Professional Documents
Culture Documents
Chemestry English Part-2
Chemestry English Part-2
QUESTION BANK
CHEMISTRY
Price
: ` 60.00
Published by :
Secretary
Gujarat Secondary and Higher Secondary Education Board,
Gandhinagar
Contribution
1
Coordination
1
Shri B. K. Patel
Shri D. A.Vankar
Shri M. P. Parmar
Expert Teachers
1.
2.
3.
Shri A. I. Patel
4.
Shri V. R. Patel
5.
Shri B. R. Patel
6.
Shri K. K. Purohit
7.
Shri M. B. Patel
8.
Shri B. A. Nayak
9.
Shri H. M. Patel
II
P R E FA C E
Uptil now , the Students had to appear in various entrance examinations for
engineering and medical courses after std-12. The burden of examinations on the side of the
students was increasing day-by-day. For alleviating this difficulty faced by the students,
from the current year, the Ministry of Human Resource Development , Government of India,
has Introduced a system of examination covering whole country. For entrance to engineering
colleges, JEE(Main) and JEE(Advanced) examinations will be held by the CBSE. The
Government of Gujarat has except the new system and has decided to follow the examinations
to be held by the CBSE.
Necessary information pertaining to the proposed JEE (Main) and
JEE(Advanced) examination is available on CBSE website www.cbse.nic.in and it is requested
that the parents and students may visit this website and obtain latest information guidance
and prepare for the proposed examination accordingly. The detailed information about the
syllabus of the proposed examination, method of entrances in the examination /centers/
places/cities of the examinations etc. is available on the said website. You are requested to
go through the same carefully. The information booklet in Gujarati for JEE( Main) examination
booklet has been brought out by the Board for Students and the beneficieries and a copy of
this has been already sent to all the schools of the state. You are requested to take full
advantage of the same also However, it is very essential to visit the above CBSE website
from time to time for the latest information guidance . An humble effort has been made by
the Gujarat secondary and Higher Secondary Education Boards, Gandhinagar for JEE and
NEET examinations considering the demands of the students and parents , a question bank
has been prepared by the expert teachers of the science stream in the state. The MCQ type
Objective questions in this Question Bank will provide best guidance to the students and we
hope that it will be helpful for the JEE and NEET examinations.
It may please be noted that this Question Bank is only for the guidance of the
Students and it is not a necessary to believe that questions given in it will be asked in the
examinations. This Question Bank is only for the guidance and practice of the Students. We
hope that this Question Bank will be useful and guiding for the Students appearing in JEE and
NEET entrance examinations. We have taken all the care to make this Question Bank error
free, however, if any error or omission is found, you are requested to refer to the text
books.
M.I. Joshi
Secretary
III
INDEX
UNIT 15 P - BLOCK ELEMENTS
48
63
76
82
94
UNIT 21 HYDROCARBONS
128
154
173
190
UNIT 25 POLYMER
209
UNIT 26 BIOMOLECULES
220
234
241
IV
of this group is carbon, so it is also known as carbon group elements. Carbon shows
catenation property due to its small size, high electronegativity and very high carbon-carbon
bond energy. Due to typical characteristic of catenation it forms number of compounds
which are studied in organic chemistry. It also forms compounds with metals and nonmetals. Group 14 elements have variation in properties like atomic radii, ionisation enthalpy
electropositive character, electronegativity, melting points and boiling points density, catenation and allotropy. The oxidation state of group 14 elements are +2 and +4. The trends in
chemical reactivity are as given in the text. The carbon shows anomalous behaviour. The
crystalline allotropes of carbon are diamond, graphite and fullerenes. The physical properties and chemical properties are as given in the text. Some important compounds of carbon
are halides of carbon, carbon disulphide, carbide compounds, carbon monoxide and carbon
dioxide, and the method of preparation and uses are as given in the text. The important
compounds of silicon are silicon hydrides having general formula
Si n H2n+2. The
1
value of bond enthalpy for silicon-silicon is 297 kJmol hence catenation character is observed in silicon and it forms limited hydride compounds, having formula Si n H2n+2 where
n = 1 to 8, and these compounds are also known as silanes. The stability of silane compounds are less compared to hydrides of carbon and hence reducing power is more. Silicon
also forms silicon dioxide known as silica and more than 22 allotropic structures are known
in which some are crystalline and some are amorphous. Silica is acidic and hence it dissolves in liquid alkali or alkaline carbonate to form silicate compounds. Silicon reacts with
only F2 and form SiF4 while reacts with Cl2 and form SiCl4. The hydrolysis of SiCl4 gives
silicic acid and the mechanism for hydrolysis are in two steps. The silicones are synthetic
materials containing Si O Si bond linkage. These compounds are polymeric substances
containing R2SiO reapeating unit. The general formula is (R2SiO)n, where R is methyl or
phenyl group. The empirical formula is R2SiO which is similar to that of organic compound,
ketone, so it is called silicone. The prepartion, properties and uses are as given in the text.
Approximately 95% of earth's crust consists of silicates and silica compounds, containing
independent SiO 44 having tetrahedral structure. The types of silicates depending upon the
number of corners (0, 1, 2, 3 and 4) of the SiO 44 tetrahedron are shared with other
tetrahedrons and based on that they are classified as given in the text. In a three dimensional
structure of SiO2, its Si4+ partially substituted by Al3+ gives aluminosilicate are called
feldspar and zeolites. In zeolites the SiO 44 and AlO54 . tetrahedron joined together in simple
way to form three dimensional network. The uses of silicates are as a molecular sieves and
shape selectives catalyst. One important catalyst of silicate is ZSM-5 used in petrochemical
industry which converts alcohol directly into gasoline.
The elements of groups 13 to 18 in the periodic table are known as p-block elementes.
The general electronic configuration of these elements is ns2np16. We have studied about the
elements of groups 15, 16 ,17 and 18 in this unit.
General introduction of elements of groups 15, 16, 17, 18
group 15
group 16
group 17
group 18
Nitrogen
Chalogens or
Halogen Group
Noble Gas
Identification
group
Oxygen group
Electronic configuration
ns2np3
ns2np4
ns2np5
ns2np6
Ne
3, to +5
2, 1, +1, +2
P, As
S, Se, Te
Cl, Br, I
Xe
3, +3, +5
2, +2, +4, +6
Sb, Bi
+3, +5
Po
+2, +4
Common name/
Group
of valence shell
Oxidation state
18
15
16
17
He
2p
Ne
3p
Cl
Ar
4p
As
Se
Br
Kr
5p
Sb
Te
Xe
6p
Bi
Po
At
Rn
Polonium element of group 16 is radioactive. Oxygen forms metal oxides with metals. Ozone is a strong
oxidising agent. Sulphur element possessess different allotropes. Out of these and allotropes are very
important. Sulphur element combines with oxygen and forms oxide compounds like SO2 and SO3. Out
of the different oxoacids of sulphur, sulphuric acid is very important. It is called 'King of Chemicals.'
Astatine element of group 17 is radioactaive. As these elements require one electron to have stable
electronic configuration, they are very reactive. As a result of this, the elements of this group are not
available in free state, but are availalbe in the combined state as negative ions. The elements of this
group form oxides, hydrogen halides, interhalogen compounds and oxoacid compounds.
Radon element of group 18 is radioactive. As the octet structure is complete in all the elements of this
group they are chemically inert. Xenon element of this group, under specific reaction conditions combine
with fluorine and oxygen elements and form fluoride and oxide compounds.
M.C.Q.
Boron Family
(1)
(2)
(a) 60 , 120
(b) 95 ,120
(c) 95 ,150
(d) 120 ,180
(3) The stability of +1 oxidation state increases in the sequence
(a) Al<Ga<In<Tl
(b) Tl<In<Ga<Al
(c) In<Tl<Ga<Al
(d)Ga<In<Al<Tl
(4) Which of the following is most acidic
(a) Na2O
(b) Mgo
(c) Al2O3
(d) Cao
(5) Cohen Orthoboric acid (H3BO3) is strongly heated, the residue is
(a) Meta boric acid
(b) Boron
(c) Al2O3, 2H2O
(d) None of above
(6)
Bauxite has the composition
(a) Al2O3
(b) Al2O3, H2O
(c) Al2O3 2H2O
(d) None of above
(7) Which one of the following is correct statement
(a) The hydroxide of aluminium is more acidic than that of boron
(b) The hydroxide of boron is basic, while that of aluminium is amphoteric
(c) The hydroxide of boron is acidic, while that of aluminium is amphoteric
(d) The hydroxide of boron & aluminium are amphoteric
(8) AlCl3 is
(a) Anhydrous & covalent
(b) Anhydrous & ionic
(c) covalent & basic
(d) coordinate & acidic
(9) Aluminium (III) chloride forms a dimer because
(a) Higher coordination number can be achieved by aluminium
(b) Aluminium has high ionization energy
(c) Aluminium belongs to III group
(d) It cannot form a trimer
(10) Aluminium has a great affinity for oxygen & its oxidation is an exothermic process. This fact
is used in
(a) Preparing thin foils of aluminium
(b) Making utensils
(c) Preparing duralumin alloy
(d) Thermite welding
(11) Which of the following is an amphoteric oxide.
(a) MgO
(b) Al2O3
(c) Cl2O7
(d) Ti2O2
(12) When Al is added to KOH solution
(a) No action takes place
(b) Oxygen is evolved
(c) Water is produced
(13) Aluminium is more reactive than iron. But Aluminium is less easily corroded than iron because
(a) Aluminium is noble metal
(14) Aluminium vessels should not be washed with materials containing washing soda since
(a) Washing soda is expensive
(b) Washing soda is easily decomposed
(c) Washing soda reacts with aluminium to form soluble aluminate
(d) Washing soda reats with aluminium to form insoluble aluminium oxide
(15) Which of the statements about anhydrous aluminium chloride is corret
(a) It exists as AlCl3 molecule
(b) 6
(c) 5
(d) 8
(c) Zn
(d) Ca
(b) Al
(18) Aluminium chloride exists as dimer, Al2Cl6 in solid state as well as in solution of non-polar solvents
such as benzene when dissolved in water gives
(d) Al2O3+6HCl
(b) Graphite
(c) Titanium
(d) SiC
(b) B3N3H6
(c) B3O3H6
(d) (BH3)3
(21) Anhydrous AlCl3 cannot be obtained from which of the following reactions
(a) Heating AlCl3 6H2O
(b) By Passing dry HCl over hot aluminium powder
(c) By Passing dry Cl2 over hot aluminium powder
(d) By passing dry Cl2 over a hot mixture of alumina and coke
(22) Diborane combines with ammonia at 120 C to give
(a) B2H6 NH3
(b) B2H6. 2NH3 (c) B2H6.3NH3
(23) Which metal burn in air at high temperature with the evolution of much heat.
(a) Cu
(b) Hg
(c) Pb
(d) Al
(24) Aluminium hydroxide is soluble in excess of sodium hydroxide forming the ion
(a) AlO 23
(c) AlO 2
(b) AlO23
5
(d) AlO3
(b) Mg(OH)2
(c) B(OH)3
(d) Al(OH)3
(b) BCl3
(c) BBr3
(d) BH3
(b) Basic
(c) Amphoteric
(32) Which is true for an element & present in III group of the periodic table
(33)
(b) acidic
(c) basic
(d) none
(b) Ag
(c) Au
(d) Fe
(36) B(OH)3 + NaOH NaBO2+Na[B(OH)4] +H2O How can this reaction is made to proceed
in forward direction.
(a) Addition of cis Benzene - 1,2-diol
(b) B3H6
(c)B4H10
(c) Na3AlF6
(b) BCl2
(c) B2Cl2
(d) CCl2
(c) B2O3
(d) As2O3
(b) Sb2O3
(b) Al2Cl6
(c) Al2O3
(d) Al(OH)Cl2
(b) C2H6
(c) PH3
(d) SiH4
(b) C2 H6
(c) Na3AlF6
(d) SiH4
(b) In
(c) Th
(59) Which one of the following statements about diborane is not true
(a) The B atoms in it are SP3 hybridised
(b) It contains two 3-centre-2-electron bonds
(c) All B-H bond lengths in it are equal due to resonance
(d) The molecule contains 12 valence electrons
8
(d) B
(d) None
(a) AlF3-6
(c) BF62
(d) SiF62
(c) Diborane
(d) Methanol
(64) The tendency of BF3 , BCl3 & BBr3 to behave as lewis acid decreases in the sequence
(a) BF3 > BCl3 >BBr3
(65) Which one of the following molecular hydrides acts a a lewis acid
(a) CH4
(b) NH3
(c) H2O
(d) B2H6
ANSWER KEY
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
d
b
a
c
a
c
c
a
a
d
b
d
b
c
c
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
b
a
b
c
b
a
b
d
c
c
c
d
c
d
c
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
c
c
c
d
a
a
d
b
c
c
d
c
b
a
a
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
d
a
c
d
a
a
c
c
a
a
c
a
d
c
a
61
62
63
64
65
c
b
c
c
d
HINTS
(2)
122
97
H
(3)
H
0
B
H
(20) AlCl3-6H2O
Al(OH)3 + 3HCl + 3H2O
(26)
(27)
(28)
(31)
(32)
(36)
(39)
(40)
(49)
(55)
B
H
3C - 2e : BHB
2C 2e : HBH
(57) 2Al(s) + 2NaOH(aq) + 6H2O(l) 2Na+ [Al(OH)4]-(aq) + 3H2(g)
sodium tetra hydroxo aluminate (III)
10
CARBON FAMILY
(1)
(B) CrO5
(C) H2SO5
(D) PbO2
(2) Soldiers of Napolean army while at Alps during freezing winter suffered a serious problem as
regards To the tin buttons of their uniforms. white metallic tin buttons got converted to grey
powder. This Transformation is related to
(A) A change in the partial pressure of oxygen in the air
(B) A change in the crystalline structure of tin
(C) An interaction with nitrogen of air at very low to temperatures
(D) An interaction with water vapour contained in the humid air.
(3)
(4)
(5)
(C)H2SiO3
(D) Na3AlF6
(8)
(7)
(D) None
The Stability of dihalides of Si, Ge, Sn and Pb increases steadily in the sequence
(A) Gex2 SiX2 SnX2 PbX2
(C) SiX2 GeX2 SnX2 PbX2
(6)
(C) Pyrex
(B) H2SiF6
(9)
(11) In lll A group Tl (thallium) shows +1 Oxidation state while other members show +3
oxidation state. Why?
(A) Presence of lone pair of electron in Tl.
(D) None
(B) PbO2
(C) Pb3O4
(D) BaO2
(D) Coconut
(B) Charcoal
(16) Carborundum is
(A) SiC
(B) AlCl3
(C)Al2(SO4)3
(C) PbO2
(D) PbHSO4
(B) PbSO4
(B) Si(OH)2F2
(C) H2SiF6
(D)Si(OH)4
(C) Chlorophyll
(D) Haemoglobin
(C) 3
(D) 4
(B) Amalgams
(B) 2
(23) Which of the following glass is used in making wind screen of automobiles.
(A) Crook's Glass
(C) ZnCO3
(D) Al2(CO3)3
(B) CaCO3
(25) In which of the following the inert pair effect is most prominent
(A) C
(B) Si
(C) Ge
12
(D) pb
(B) Acids
(D) CuSO4
(27) Which of the following glass is used to make lenses and prisms
(A) Flint
(B) Jena
(C) Pyrex
(D) Quartz
(B) PbO
(C) PbO2
(D) Pb4O3
(31) Name of the structure of silicates in which three oxygen atoms of [SiO4]4 are shared is
(A) pyrosilicate
(B) Lead
(C) Tin
(D) Nickel
(B) Pb+Zn
(C) Pb+Sn
(D) Sn+Zn
(34) Which of the following statement is correct with respect ot the property of elements in the
carbon Family with an increase in atomic number their.
(A) Atomic size decreases
(B) Graphite
(C) FeS
(D) Pb
(B) Mg2C3
(C)B4C
(D) La4C3
(B) TiC
(C)SiC
(D) CaC2
(B) NH+4
(C) SCl4
(D) SO42
(B) PbO2
(C) Pb3O4
13
(D)PbSO4
(D) None
(B) Pb(NO2)2, O2
(C) Pb2O3
(D) Pb3O4
(C) 80
(D) 70
(C)N2O5
(d) NO2
(B) PbO2
(B) 20
(B) NH4NO3
(B) PbO2
(C) Pb3O4
(D) Pb(CH3COO)2
(C) B
(D) Pb
(C) Mixed
(D) Amphoteric
(B) Ca
(B) Super
(B) Lead
(C) Tin
(D) Copper
(C) Ge
(D) C
(C) C2H6
(D) CO2
(C) HI
(D) HBr
(B) Sn
(B) C2H2
(B) HF
14
(D) None
(56) SiCl4 on hydrolysis forms 'X' & HCl Compound 'X' loses water at 1000oC & gives 'Y'. Compound
'X' & 'Y' are respectively.
(A) H2SiCl6, SiO2
(B) H2SiO4, Si
(C) SiO2, Si
(B) PbNO3 + NO
(B) Si
(C) Ge
(D) Sn
(B) Acidic
(C) Neutral
(D) Amphoteric
(60) PbO2 is
(A) Basic
(D) R3Si4O4
(B) TiCl4
(C) SiCl4
(D) CCl4
(B) Insulator
(B) CO + O2
(C) CO2+ O2
(D) C + H2 + N2
(65) The element evolving two different gases on reaction with conc. H2SO4 is ______.
(A) P
(B) C
(C) Hg
(D) S
(B) CO
(C) CO2
(D) CaCo3
(D) Water
(C)+3, +4
(D) +4
(B) Conc.H2SO4
(B) +1, +2
15
Answer Key
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
D
B
B
B
C
C
B
A
A
C
B
A
C
B
C
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
A
B
C
D
A
B
B
c
D
D
C
A
C
C
A
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
D
B
C
D
C
B
B
D
C
C
D
C
C
D
A
16
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
A
A
A
D
C
C
C
A
B
A
D
A
D
C
D
61
62
63
64
65
66
67
68
69
A
D
C
C
B
A
C
A
D
HINTS
(2)
Grey tin is very brittle & easily crumbles down to a powder in very cold climates
Grey Tin
White Tin
(Cubic)
(Tetragonal)
The change of white tin to grey is accompanied by increase in volume. This is called disease
or tin Plague.
(3)
Zeolite have SiO4 & AlO4 tetrahadrones linked together in a three dimensional open structure
in which four or six member ring predominate. Due to open chain structure they have cavities
& can take up water & other small molecules.
(4)
Crook's glass is a special type of glass containain cerium oxide. It does not allow the passage
of ultraviolate rays & is used for making lense.
(5)
Due to inert pair effect, stability of +2 oxidation state increases as we move down this
groupSiX2 GeX2 SnX2 pbX2
(6)
Sodium oxalate react with conc. H2SO4 to form CO & CO2 gas
(10) tin is oxidized to meta stannic acid when it is treated with nitricacid
Sn + 4 HNO3 H2SnO3 + 4NO2 + H2O
(11) Inert pair effect become significant for 6th & 7th period of p- block element.
(12) Carbon Suboxide has linear structure with C - C bond lenth equal to 130 Ao & C - O
bond length equal to 120Ao O = C = C = C = O O C C C O+
(13) Pb3O4 is mixed oxide. It can be represented as 2PbO PbO2
(14) Noble gas are found in very minute amount in atmosphers. These are separated from each other
by using coconut char coal. Which absorb different gas at different tempera tures.
(15) SolidCO2 is known as dry ice because it evaporate at -18oC without changing in Liquid state.
(17) When hydrogen peroxide reacts with PbS then they forms PbSO4
(18) Silicon occurs in combined state in nature as silica, SiO2
1s2
2s2
(21)
No of unpaired e- in p = 2.
(22) Metal oxides or some salts are fused with glass to imparted colour of glass.
(24) Al2(CO3)3 is less soluble in water than Na2CO3, ZnCO3
(25) inert pair effect is most prominent in Pb because from top to bottom due to increase in number
of shells.
17
(47)
O
O
O Si O Si O
O
O
18
(55) Solid CO2 is called dry ice because it changes to vapour state directly without changing to liquid
state.
(57) HNO3 is best solvent for lead
Pb + 4HNO3
Pb (NO3)2 + 2NO2 +2H2O
SiO2 + 3C
SiC + 2CO2
1
O Pb (CH3 COO)2 + H2O.
2 2
19
NITROGEN FAMILY : 15
(1)
Which of the following elements does not form stable diatomic molecules
(A) Iodine
(2)
(C) HNO3
(d) NO2
(B) NO
(C) N2O5
(B) Zn
(C) Cu
(D) Ag
(B) NCl3
(C)NBr3
(D) NI3
(B) H4P2O7
(C)HPO3
(D) H3PO4
(C) As
(D) Bi
(9)
(B) N2O
(8)
(7)
Which of the following metal produces nitrous oxide with dil HNO3
(A) Fe
(6)
(5)
(D) Oxygen
(4)
(C)Nitrogen
(3)
(B) Phosphorous
(B) P
(B) KNO3
(C) NaNO2
(D) NaNO3
(D) H2 is evolved
(B) HNO3
(C) NH3
(D) PH3
(D) It is paramagnetic
(B) PCl4+
(C) PCl6-
(B) H6P4O13
(C) H5P5O15
(D) H7P5O16
(19) Which catalyst is used in the haber process for the manufacture of NH3
(A) Pt
(B) Fe+Mo
(C) CuO
(D) Al2O3
(B) PH3
(C) SbH3
(D) ASH3
(C) Pb(OH)Cl
(D) Na2HPO4
(B) BiOCl
(22) Which of the following is manufactured from the molecular nitrogen by bacteria
(A) NO3
(B) NO2
(D) Ammonia
(23) Which of the following Tendencies remains unchanged on going down in the nitrogen family
(A) Highest Oxi. State
(24) (NH4)2 Cr2O7 on heating liberates a gas. The same gas will be obtained by
(A) heating NH4NO2
(25) When plants and animals decay, the organic N is converted in to inorganic N. The inorganic
N is in the form is
(A) NH3
(B) Elements of N
21
(C) Nitrates
(D) Nitrides
(B) Mg3(PO4)2
(C) H3PO4
(D) P2O5
(C) CO and H2
(C) N, H, O3
(B) PH3
(C) ASH3
(D) SbH3
(30) The element which catches fire in air at 30oC and is stored under water is
(A) Calcium
(B) Sodium
(C) Phosphorous
(D) Zinc
(C) H3PO4
(D) None
(C) H3PO2
(D) NF3
(B) PF3
(C) SbCl3
(D) NF3
(B) PH3
(C) AsH3
(D) SbH3
(B) H4P2O7
(B) H3PO4
(35) The cyaide ion, CN, N2 are iso electronic. But in contrast to CN, N2 is chemically inert because
of
(A) Low bond energy
(37) A mixture of ammonia and air at about 800oC in the presence of Pt gauze forms
(A) N2O
(B) NO
(C) NH2OH
(D) N2O3
(C) Al2O3
(D) Sb2O3
(B) SeO2
(B) Brine
(C) Water
22
(D) Mercury
(B) NH4OH
(C) NH4Cl
(B) Chlorobenzene
(D) Dichlorobenzene
(B) White
(C) Black
(C) AsH3
(D) BiH3
(B) CO2
(C) Cl2
(D) CCl3NO2
(B) NH3
(C) P4O6
(D) P4O10
(B) NaH2PO2
(C) Na3HP2O6
(D) Na4P2O7
(B) PH3
(B) 4
(C) 5
(D) 7
(B) Arsine
(C) Phosphine
(D) Ammonia
(C) AsH3
(D) SbH3
(B) PH3
(B) PH3
(C) AsH3
(D) SbH3
(C) NO 2 and OH
(D) -3,+3,+4
(C) Sb
(D) Bi
(B) Tin
23
(B) 2
(C) 3
(D) 4
(B) Ammonia
(D) Urea
(B) H2
(C)NO2
(D) NH3
(B) PH3
(C) SbH3
(D) AsH3
(59) Aquaregia is
(A) 1:3 conc. HNO3 and conc. HCl
(B) SbH3
(C) NH3
(D) PH3
(C) AsH3
(D) SbH3
(C) AsH3
(D) SbH3
(B) PCl3
(C) AsCl3
(D) All
(B) P2O3
(C) Sb2O3
(D) Bi2O3
(B) As2O3
(C) SbCl2
(D) As2H3
(C) N2O + Ca
(D) (NH4)2Cr2O7
(C) NH4NO2
(D) Ba(NO3)2
(C) NaNO2
(D) NaNO3
(B) PH3
(B) PH3
(B) Ca3N2
(B) KNO3
24
(B) N2O3
(C) N2O4
(D) N2O
(C)N2H2
(D) N3H
(B) N2H4
(B) (NH4)2SO4
(B) H4P2O7
(C) HPO3
(D) H3PO4
(C) PH3
(D) SbH3
(C) SbCl3
(D)
(B) NH3
(B) PF3
NF3
(B) Bi(OH)3
(C) BiOCl
(D) BiOCl2
(D) Hg(OH)2
(B) IV A Group
(B) Phosphorus
(C) Arsenic
(D) Antimony
(78) Which of the following elements of group VA does not show allotropy
(A) N
(B) Bi
(C) P
(D) As
ANSWER KEY
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
B
C
A
D
B
A
A
A
D
A
D
A
B
C
A
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
D
C
C
B
A
D
A
A
A
A
A
A
B
A
C
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
A
D
D
A
D
D
B
A
D
D
C
A
D
D
A
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
25
D
B
D
D
A
B
A
A
B
C
D
D
D
A
B
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
A
B
A
B
C
B
C
A
D
D
D
A
B
D
C
76
77
78
A
A
B
HINTS
(4)
(5)
(6)
NF3
It is least basic bacause of high electronegativity of 3F atoms. The lone pair present on
nitrogen atom is not easily available for donation.
(7)
(8)
(9)
COOH
|
(11) C12 H22O11
HNO 3
COOH
+ H2O
(24) (NH4)2Cr2O7
N2 + Cr2O3+4H2O
NH4NO2
N2+2H2O
(28) NH4NO3
2H2O + N2O
(30) because of its very low ignition temp (303K) it is always kept under water.
(32) 3H2O + PCl3 H3PO3 + 3HCl
(33) Due to absence of d - orbital in N - atom, it can't accept e from H2O for hydrolysis of NF3
Pt
4NO + 6H O
(37) 4NH3 + 5O2
2
800 C
NH3
BP 238.5
PH3
185.5
AsH3
SbH3
210.6
254.6
OXYGEN FAMILY
(1)
(2)
(9)
(B) Matalloids
(C) Radioactive
(D) Plymorphic
(B) Polyzone
(C) Trizone
(D) Ozone
(B) HCl
(C) H2SO4
(D) HNO2
(B) Na2SO4
(C) CaCl2
(D) P4O10
(8)
(D) S8
(7)
(C)S4
(6)
(B) S2
(5)
(D) CO2
(4)
(C) SO2
(3)
(B) O2
(B) Cr2O3
(C) V2O3
(D) MnO2
Which of the following is the best scientific method to test presence of water in a liquid
(A)Taste
(B) Smell
(B) CdSO4
(C) PbSO4
(D) Bi2(SO4)3
(10) When sulphur is boiled with Na2SO3 solution, the compound formed is
(A) Sodium Sulphide
(B) 6
(C) 8
(D) 1
(D) H2SO4 + S
(C) KO2
(D) BaO2
(15) Which of the element of the oxygen family is most poisonous to human race
(A) O
(B) S
(C) Se
27
(D) None
(D) None
+
(B) H2S
(C)H2Te
(D) H2Se
(19) Among H2O, H2S, H2Se and H2Te the one with highest boiling point
(A) H2O
(B) H2Te
(C) H2S
(D)H2Se
(B) O2 + CO
(C) O2 + H2
(21) Carbogen is
(A) Pureform of C
(B) COCl2
(22) The products of the chemical reaction between Na2S2O3, Cl2 and H2O are
(A) S+ HCl + Na2S
(25) Aqueous solutions of H2S and SO2 when mixed together yield
(A) Sulphur and water
(B) CO2
(C)CaO
(D) ZnO
(C)Water
(B) K2Cr2O7
(C)KMnO4
(D) All
(C) Sulphite
(D) Sulphid
(B) Sulphurate
(31) The final acid obtained during the manufacture of H2SO4 by contact process
(A) H2SO4(conc.)
(B) H2SO4(dil)
(C) H2SO4
(D) H2S2O7
(B) MnO2
(C) Al2O3
(D) CrO3
(C) Hydrolysis
(B) Oxidisation(oxide)
(37) When conc.H2SO4 comes in contact with sugar it becomes black due to
(A) Hydrolysis
(B) Hydration
(C) Decolourisation
(D) Dehydration
(C) H2S2O7
(D) H2S2O8
(B) H2SO4
(B) H2S
(C) S2O
(D) SO3
(D) None
(C) S2 O32
(D) S2 O 72
(C) Ur
(D) Ag
(42) Oleum is
(A) Castor oil
(B) S2 O52
(B) S
29
(B) Ba(OH)2
(C) KOH
30
(D) Zn
(D) PH3
(D) H2S2O7
(D) KI
(D) 0oC
(D) H2S2O3
(D) None
(D) H2O
(D) N2O
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
C
D
D
D
C
A
C
D
C
D
A
A
A
C
C
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
A
C
C
A
A
D
B
C
C
A
A
B
D
A
C
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
D
A
A
A
B
A
D
B
D
C
D
C
D
B
B
31
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
B
B
B
A
D
A
C
A
C
A
B
D
C
C
A
61
62
63
64
65
66
67
68
69
70
71
C
B
B
B
A
C
C
D
B
B
B
Hints
(7)
O
O
||
||
(43) S2O 72- O S O S O
||
||
O
O
(54) Sulphur -
(1) monoclinic
(2) Rhombic
(3) Plastic
O
F
97
1.48A
F
O
O
F
32
HALOGENS FAMILY
(1)
(2)
(3)
(4)
(B) Phosphine
(B) Chloroform
(B) KClO4
(C) KClO2
(D) KIO3
(7)
(D) Na2SO4
(D) Cryolite
(C) Ratherlford
(D) Sheele
(9)
(C) Na2S
(A) Caliche
(8)
(B) Na2S2O3
(B) Priestley
(B) I2
(D) SO2
(10) Chlorine reacts under various conditions with sodium hydroxide to give
(A) Sodium Chloride
(B) Red
(C) Colourless
(D) Yellow
(C) HBr
(D) HI
(D) Chlorine
(B) HCl
(B) I
(C) Br
(D) Cl
(C) I2
(D) F2
(B) Br2
(B) Cl
(C) Br
(D) I
(B) S2P6
(C) S2P4
(D) S2P5
(B) K2Cr2O7
(C) HNO3
(D) HCl
(22) Aqueous solution of which of following acid can not be kept in bottle of glass
(A) HF
(B) HCl
(C) HBr
(D) HI
(B) Cl
(C) Br
(D) I
(C) HBr
(D) HI
(B) HCl
(26) Fluorine is stronger oxidizing agent than chlorine in aqueous solution. This is attributed to
many factors except.
(A) Heat of dissociation
(B) e-affinity
(27) Mark the element that displaces 3 halogens from their compound
(A) F
(B) Cl
(C) Br
(D) I
(B) Cl
(C) Br
(D) I
(29) Which of following arrangement for 3 halogens Cl, Br, I when placed in order of
increasing e-affinity
(A) Cl, Br, I
(B) I, Br, Cl
(C) Br, Cl , I
34
(D) I , Cl , Br
(B) Br
(C) Cl
(D) F
(C) O3
(D) N2X
(B) CH4
(34) Inisolation of F., a number of difficulties were encounted. Which statement is correct?
(A) Potential required for discharge of F. ions is the lowest.
(B) F. reacts with most glass vessel
(C) F has great affinity for H.
(D) Electrolysis of aqueous HF gives ozonised O2
(35) Chlorin gas is dried over
(A) CaO
(B) NaOH
(C) KOH
(C) Cleansing
(B) Sterilisation
(D) HI & KI
(C) I2O5
(D) I4O9
(D) H - bonding
(B) KI & I2
(B) BrO2
(43) HBr & HI reduce Sulphuric acid, HCl can reduce KMnO4 & HI can reduce
(A) H2SO4
(B) KMnO4
(C) K2Cr2O7
(D) None
(C) HBr
(D) HI
(B) HCl
(47) The halide NaF has high melting point than NaCl , NaBr, & NaI because
(A) Minimum ionic character
(B) Br
(C) Al
(D) Ca
(B) Sn
(C) S
(D) F2
(51) Which one of following in aqueous solution gives a white precipitate with per chloric acid
(A) NaCl
(B) KCl
(C) MgCl2
(D) FeCl3
(52) NOCl is used as a bleaching agent & storilisng agent It can be synthesized by action of
(A) NaCl with H2O
(53) A one litre flask is full of brown bromine vapour intensity of brown colour of vapour will not
decrease a appriciable on adding to flask some of
(A) Pieces of marble
(B) Crystallization
36
(C) Sublimation
(56) Hydrogen has a tendency to gain one e to acquire helium configuration. In this respect
it resembles.
(A) Halogens
(B) Actinides
(57) The compound added to table salt for maintaining proper health is
(A) KCl
(B) KBr
(C) NaI
(D) MgBr2
(B) Cl2
(C) Br2
(D) I2
(B) BCl3
(C)MgCl2
(D) NaCl
(62) Concentrated H2SO4 can not be used to prepare HBr from NaBr because it
(A) reduces HBr
(63) When Fluoride is heated with conc. H2SO4 & MnO2 the gas evolved is
(A) F2
(B) SF
(C) HF
(D) None
(64) Unlike other halogens Fluorine does not show higher oxidation states because
(A) It is highly electionegative
(B) OF2
(C) SF4
(D) O2F2
(C) FeSO4
(D) NH4SO4
(B) CaSO4
(67) Among Cl, Br, I correct order for being oxidized to dihalogen is
(A) I Cl Br
(B) CI Br I
(C) I Br CI
(D) Br I CI
(69) When thiosulphate ion is oxidized by iodine , which one of following ion is produced?
(A) SO 32
(B) SO 24
(C) S4 O 62
(D) S2 O 62
(C) HBr
(D) HI
(B) HCl
(71) When Cl2 is passed through hot & Conc. Solution of KOH following compound is formed.
(A) KCl
(B) KClO3
(C) KClO2
(D) KClO4
(B) HBr
(C) HClO3
(D) HCl
(C) KI2
(B) KI2
(D) KI3
(79) When Cl is passed over dry slaked lime at room temperature, main reaction product is,
(A) Ca(ClO2)2
(B) CaCl2
(C) CaOCl2
(D) Ca(OCl2)2
(C) HBr
(D) H2S
(B) NaClO2
(C) NaClO3
38
(D) None
(B) ClO2
(C) Cl2O6
(D) Cl2O7
(C) I2
(D) Cl2
(B) F2
(85) Electrolysis of a liquid resulted in formation of Hydrogen at cathode & Cl2 at anode.
Liquid is
(A) Pure water
(B) HOI
(C) HOIO2
(D) HOIO3
(87) Manufacture of Bromine from sea water, the mother liquor containing bromides is treated
with
(A) CO2
(B) Cl2
(C) I2
(D) SO2
(88) Formula of some fluorides are given. Which of them will combine with fluorine?
(A) IF5
(B) NaF
(C) CaF2
(D) SF5
(C) Br
(D) I
(B) F
(90) A solution of HCl in water is good conductor while gaseous Hydrogen chloride is not .
This is because
(A) Water is good conductor of electricity
(C) Gas can not conduct electricity but water can (D) None of these
(91) Bleaching action of bleaching powder is due to liberation of
(A) Chlorine
(92) What products are expected from disproportion reaction of hypochlorous acid.
(A) HClO3 & Cl2O
(93) Mixture of conc. HCl & HNO3 made in 3:1 ratio contains
(A) ClO2
(B) NOCl
(C) NCl3
(D) N2O4
(C) Br
(D) F
(C) Hydrolysis
(C) P
(D) S.
(B) I
(B) Reduction
(B) C
39
(B) Na
(C) F
(D) I.
(C) Cl
(D) All
(B) Cl+
(100) Which of following sequence is correct with refrence to oxidation number of iodine
(A) I2 < ICl < HI < HIO4
(C) Hg(CN) Cl
(D) Hg [Hg(CN)2Cl2]
(B) KBr
(C) CaCl2
(D) AgF
(B) SO2
(C) ClO2
(D) SiO2
(C) CCl4
(D) Alcohol
(B) CCl4
(C) C2H5Cl
(D) C2H6
(B) CaO
(C) CaO(Cl).
(D) CaCl(OCl)
(B) CaCO3
(C) CaSO4
(D) Ca(OH)2
(109) Which is formed when F reacts with hot & conc. Sodium Hydroxide.
(A) O2
(B) O3
(C) NaO
(D) HF.
(B) Cl2
(C) CrOCl2
(D) CrO2Cl2
(112) Amongst LiCl , RbCl , BeCl2 & MgCl2 , max. & min. ionic character will be shown by
(A) LiCl , MgCl2.
BeCl2
(D) MgCl2,
(B) AgCl
(D) None
(114) The alkali metal halide are soluble in water but LiF is insoluble because
(A) It's Amphoteric
(115) Which of following is present as an active ingredient in bleaching powder for bleaching action
(A) CaCl2
(B) CaOCl2
(C) Ca(OCl)2
(D) CaO2Cl
(C) Cl2O6
(D) ClO4
(C) HBr
(D) HI
(B) Cl2O
(B) HCl
(118) When KBr is treated with concentrated H2SO4 redish brown gas evolved, gas is
(A) Mixture of Br & HBr
(C) Bromine
Answer Key
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
B
A
D
A
C
B
B
A
A
D
A
A
D
C
A
B
D
D
D
A
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
D
A
D
A
B
B
A
A
B
C
C
A
D
A
D
A
D
B
B
D
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
B
C
D
A
B
D
B
A
D
C
B
C
A
C
B
A
C
D
D
D
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
41
B
B
C
B
A
B
C
A
C
A
B
A
A
D
B
A
A
D
C
A
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
A
A
D
B
C
C
B
A
B
B
C
D
B
A
B
A
A
C
A
D
101
102
103
104
105
106
107
108
109
110
111
112
113
114
115
116
117
118
B
D
A
C
B
B
D
D
A
B
D
B
B
C
C
C
A
C
HINTS
(1)
(2)
(3)
Iodine has the least affinity for water and is only slightly soluble in it . However it is dissolved
I2 + I
I3 (Complex)
(4)
2KClO3 + I2 2KIO3
+ Cl2
(5)
(6)
The acidic strength of oxy acids decreases down wards in a group. The correct order of acidic
C strength of oxy - acids of Halogens is HClO4 > HBrO4 > HIO4
(7)
Carnellite is KCl. Mg Cl2.6H2O. The mother liquor remain after crystallisation of KCl from carnellite
contains about 0.25% of Bromine as MgBr2 or KBr.
(9)
Cold
(10) 2NaOH(dil) + Cl2
NaCl + NaClO + H2O. Sod. Hypochlorite.
heat
6NaOH(conc) + 3Cl2
5NaCl + NaClO3 + 3H2O Sodium chlorate.
(12) HF is weakest acid. Since it is on able to give H + ions which are trapped in H - Bonding.
(69) 2Na2S2O3 + I2 2NaI + Na2S4O6
(70) HF is liq. Because of int . molec. H - Bond
(71) 6KOH + 3Cl2 5KCl + KClO3 + 3H2O
(72) Cl2 + 2NaBr 2NaCl + Br2
(73) HClO H+ + ClO(74) Br2 + 2KI I2 + 2KBr
(75) 2NaCl + 2H2O 2 NaOH(aq) + Cl2(g) + H2(g)
(76) I2 + 10HNO3 2HIO3 + 10NO2 + 4H2O
(77) MnO 2 + 4HCl MnCl2 + 2H 2 O + Cl2
(4 )
(2 )
42
(78) KI + I2 KI3
(79) Ca(OH)2 + Cl2 CaOCl2 + H2O
(80) Cl2 + 2Br 2Cl + Br2.
(81) 2KBr + H2SO4 K2SO4 + 2HBr
(82) 2NaOH + Cl2 NaClO + NaCl + H2O
(83) 2HClO4 H2O + Cl2O7
(84) H2 + F2 2HF (anode)
(85) 2NaCl + 2H2O 2NaOH + Cl2 + H2 (cathode)
(86) I2 + 10HNO3 2HIO3 + 10NO2 + 4H2O
(87) Mg Br2 + Cl2 MgCl2 + Br2
(88) IF5 + F2 IF7
(89) 2F2 + 2H2O 4HF + O2
H2O
(90) HCl
H (ag ) Cl
43
Cl
(107) CaCl(OCl)
Ca
O
Cl
44
(2)
(4)
(C) Rectile
(D) Haematite
(D) Is diatomic
(D) Ramsay
(C) Helium
(D) Xenon
(C) Methane
(D) Xenon
(7)
(A) Monoatomic
(A) Argon.
(6)
Molecules of noble gas do not posses vibrational energy bec. Noble gas is
(A) Rayleigh
(5)
(3)
(B) Argon
(8)
Monazite is source of
(A) He
(9)
(B) Kr
(C) Ar
(D) Ne.
(B) Beryllium
(C) Aluminium .
45
(D) Krypton.
(16) Which of following noble gas does not have octate of e - in outer most shell.
(A) Ne
(B) Rn
(C) Ar
(D) He
(B) 2%
(C) 3%
(D) 4%
(B) Ne
(C) Ar
(D) Xe.
(A) XeO6
(B) H XeO 4
(C)
XeO 4
(D) Xe.
(B) He
(C) Ar.
(D) Rn
(C) N2.
(D) Argon.
(B) O2
(B) He
(C) Ar
(D) Kr
(C) Kr & Ne
(D) Ar & Xe
(B) Ar & Ne
(B) Rutherford
(D) Dorn
(B) Reducing
(C) Un reactive
(C) Xe
(D) Ne
(B) He
46
(B) Duterium .
(C) He
(D) Krypton
(C) SF4
(D) CF4
(C) 18
(D) 8
(D) 1S2
(B) Ar
(C) Ne
(D) He
(B) XeO
(C) XeO2
(D) Xe
(B) HeF4
(B) 2
Answer Key
1
2
3
4
5
6
7
8
9
10
B
B
A
D
C
B
A
A
A
B
11
12
13
14
15
16
17
18
19
20
B
D
A
C
A
A
B
A
D
A
Hints
(26) all the xenon fluorides are strongly oxidizing
(27) XeF2, XeOF2, XeF4, XeOF4, XeF6, XeO3
2
(28) 1H 1H 2He
21
22
23
24
25
26
27
28
29
30
D
D
B
D
C
A
C
C
B
D
31
32
33
B
D
A
Blo ck
periodic table
Groups 1 to 2
s-Block
Groups 13 to 18
p-Block
Groups 3 to 12
d-Block
f-Block
The elements which in their ground state or any one of their oxidation states, d-orbital is
incompletely filled are called transition elements.
Amongst the d-block elements Zn, Cd and Hg do not act as transition elements.
In the first transition series, atomic radii decrease from Sc to V, while atomic radius remains
same in elements Cr to Cu and the atomic radius of Zn is found increasing instead of
decreasing.
Not much difference is observed in first and second ionization enthalpies of two neighbouring
transition elements but the value of second ionization enthalpy of Cr and Cu are more than
those of their neighbouring elements.
Most of the ionic and covalent compounds of transition elements are coloured.
The capacity to form complex compounds is much more than other elements because of
definite characteristics of transition elements.
In the formation of crystals of transition metals, the voids are there in which non-metal
elements (H, C, N, B) arrange and form interstitial compounds.
Scientists Hume and Rothery suggested the rules for the alloys and accordingly alloys having
useful properties are obtained from transition metal elements.
48
The compounds of transition element- KMnO4 and K2Cr2 O7 are very useful in laboratory and
in synthesis of organic compounds.
f-Block elements (Innertransition elements)
f-Block elements are divided in to (1) Lanthanide series and (2) Actinide series.
Lanthanide series
Elements of lanthanide series are called lanthanoids which are shown by symbol Ln.
49
MCQ
1.
Whieh groups of elements are called d-block elements in modern periodic table ?
(A)
2.
6.
7.
8.
9.
11.
12.
3 to 12
(D)
13 to 18
(B)
(C)
(D)
(B)
(C)
(D)
(B)
(C)
(D)
(C)
Transition elements
(B)
(D)
[ Rn ] 5f o 6d 2 7s2
(C)
[ Rn ] 5f 2 6d 2 7so
(B)
[ Rn ] 5f 2 6d 2
(D)
[ Rn ]
7s2
5f 6d 2 7so
(B)
(C)
(D)
(B)
(C)
(D)
10.
(C)
Which elements transist between more electropositive and less electropositive elements ?
(A)
5.
3 to 10
4.
(B)
3.
1 to 2
Ac, Rt
(B)
Ac, Re
(C)
Rf, La
(D)
( n - 1) d 1-9
(C)
(n 1)d1-10 ns1
ns1- 2
(B)
(D)
(n-1)d1-9 ns2
[Ar] 3d 4
4s 2
(B)
[Ar] 3d 5
(C)
[Ar] 3d 5
4s1
(D)
[Ar] 3d 5 3s1
4s 2
[Ar] 3d 9
4s 2
(C)
(B)
[Ar] 3d 9 3s 2
(D)
[Ar] 3d10
50
4s1
Y, Rf
13.
14.
15.
16.
17.
18.
Ru
Pt
(A)
(C)
(B)
(D)
19.
20.
21.
2t
22.
23.
(A) yellow
(B) violet
(C)
What is colour of aqueous solution of [Co(NH3)6]3+
(A) violet
(B) yellowish orange (C)
51
pink
(D)
green
red
(D)
green
24.
25.
Cr 3+ , Mn 2+
(B)
Co 2+ , Mn 3+
(C)
Co 2+ , Mn 2+
(D)
Co 3+ , Mn 2+
(C)
Fe3+
26.
(B)
Ti3+
27.
V4+
Cr 2+ , Cu +
a.
b.
c.
d.
e.
Column-B
colourless
pink
purple
blue
vilot
1.
2.
3.
4.
V
Ti3+
Ti4+
Mn2+
(A)
1 d
2c
3a
4e
(B)
1 d
2c
3a
4b
(C)
1 d
2e
3a
4b
1 e
2c
Match column-A and B.
Column-A
1. NiCl2 . 6H2O
2. Co (NO3)2 . 6H2O
3. FeCl3
4. CuSO4 . 5H2O
3b
4a
4+
Column-B
a.
b.
c.
d.
e.
pink
colourless
blue
green
yellow
(A)
1 e
2c
3b
4a
(B)
1 d
2c
3b
4e
(C)
1 d
2a
3c
4b
(D)
30.
Ti +4, Mn +3
(D)
29.
Cu +
Ti4+ Cu+1
(D)
Column-A
28.
(D)
1 d
2a
3e
4c
Which catalyst is used to prepare SO3 from SO2 in contact process of production of H2SO4 ?
(A) NO
(B) V2O 5
(C) Fe
(D) Ni
Which of the following trantion metal ion has magnetic moment 3.87 BM ?
(A) Co2+
(B) Co3+
(C) Fe2+
(D) Fe3+
52
31.
32.
33.
34.
35.
36.
37.
38.
39.
40.
In which of the following compound of trantion metal ion has 4.90 BM magnetic momentum?
(A) KMnO 4
(B) NiCl2
(C) CoCl2
(D) FeSO 4
Which of the following sentence is not suitable for the capacity of transition metal to form complex
compounds ?
(A) Transition metal ions are small in size.
(B) Nuclear charge of trantion metal ion in comparatively more.
(C) Co-ordination covalent bond is not directional.
(D) Transition metal ions possesses different oxidation states.
Which of the following rules to prepare alloys should be obey ?
(A) Difference in atomic radii should be less than 15%.
(B) Valence electron configuration should not be equal.
(C) Atomic volume should not same.
(D) Crystal lattice structure are different.
What is the difference in atomic radii of two metallic elements to prepare alloys ?
(A) 15%
(B) more than 15%
(C) less than 15%
(D) 24.5 %
What is the difference of atomic radii of Au and Cu in 22 carate gold ?
(A) 15%
(B) more than 15%
(C) less than 15%
(D) 24.5%
Mn, Co, Cu metals are generally useful to prepare alloys because
(A) the difference in their atomic volume is more than 15%.
(B) the difference in their atomic volume is less than 2%.
(C) the difference in their atomic volume is 15%.
(D) the difference in their atomic volume is 2%.
Which alloy is used in preparation of coins ?
(A) Brass
(B) Bronze
(C) German-Silver
(D) Nichrome
Which alloy is used in preparation of antic - piece ?
(A) Nitinol
(B) Bronze
(C) Cupronickle
(D) German-Silver
Which alloy possesses facinating property of memory ?
(A) Brass
(B) Nitinol
(C) Nichrom
(D) Cupronicle
Match column-A and column-B properly.
Column-A
Column-B
1. Brass
a. Ni (60%) Cr (40%)
2. Bronze
b. Cu (80%) Sn (20%)
3. Cupronicle
c. Cu (90%) Sn (10%)
4. Nicnrom
d. Cu (70%) Zn (30%)
e. Cu (75-85%) NI (25-15%)
53
(A)
1 d
2c
3e
4a
(B)
1 d
2c
3e
4b
(C)
1 d
2e
3a
4b
1 e
2c
3a
Where amalgum alloy is used ?
(A) In electric heater
(C) To make surgical appliaces
Match Column-A and Column-B properly.
4d
(D)
41.
42.
(B)
(D)
In space reaserch
In filling tooth cavity
1.
2.
3.
4.
Column-A
Stainless steel
Bronze
Nitinol
German silver
Column-B
(A)
1 e
2d
3b
4c
(B)
1 e
2c
3b
4d
(C)
1 e
2c
3a
4b
a.
b.
c.
d.
e.
In reveting
In antic piece
To make coins
To make surgical appliances
Cu (75-85%) NI (25-15%)
(D)
43.
44.
45.
1 e
2c
3a
4d
Which of the following proportion of constituent is present in amalgam alloys ?
(A) Hg (50%) Ag (35%) Sn (12%) Cu (3%)
(B) Hg (50%) Ag (35%) Sn (12%) Cu (3%) Zn (0.2%)
(C) Hg (50%) Ag (12%) Sn (35%) Cu (3%) Zn (0.2%)
(D) Hg (50%) Ag (35%) Sn (3%) Cu (12%)
Fe Cr2 O 4 + Na 2 CO 3 + O 2 mention which product is obtained ts ?
(A)
Na 2 CrO 4 + Fe3O 4 + CO 2
(B)
Na 2CrO 4 + Fe2O3 + CO 2
(C)
Na 2 Cr2 O 7 + Fe 2 O 3 + CO 2
(D)
Na 2 Cr2 O 7 + Fe 2 O 3 + CO
46.
(A) 2:4:7
(B) 4:6:6
(C) 4:8:7
What will be mole ratio of product in the following equation ?
(D)
4:8:4
(D)
8:2:6
Fe Cr2 O 4 + Na 2 CO 3 + O 2 Na 2 CrO 4 + Fe 2 O 3 + CO 2
(A)
8:2:8
(B)
8:4:8
(C)
54
4:4:8
47.
X + H + Y + Na + + H 2 O
48.
49.
50.
51.
(A)
X = Na 2 Cr2 O 7
Y = Na 2 Cr O 4
(B)
X = Na 2 Cr2 O 7
Y = Na 2 Cr2 O 7
(C)
X = Na 2 Cr2 O 4
Y = Na 2 Cr2 O 7
(D)
X = Na 2 Cr2 O 4
Y = Na 2 Cr O 4
(A)
X = Na 2 Cr2 O 7
Y = Fe3 O 4
(B)
X = Na 2 Cr O 4
Y = Fe3 O 4
(C)
X = Na 2 Cr O 4
Y = Fe 2 O 3
(D)
X = Na 2 Cr2 O 7
Y = Fe 2 O 3
X + KOH + O 2 Y + H 2 O
Y + H 2SO 4 + Z + K 2SO 4 + MnO 2 + H 2 O
What are X, Y and Z in above reactions ?
52.
(A)
(B)
(C)
(D)
53.
(D)
2:2
(D)
2:2:1:1
54.
55.
56.
57.
58.
59.
60.
61.
62.
63.
64.
65.
(B)
(D)
(A)
K 2 Cr2 O 7
(B)
KMnO 4
MnO 2
(C)
As corrosion inhibitors
In preparation of azo compound
(D)
(B)
(D)
Zinc chloride
Mercury Amalgam
(A)
(C)
FeSO 4
(B)
K 2Cr2O7
KMnO 4
(D)
K 2 MnO 2
K 2 MnO 4
(B)
( n - 2 ) f 0-14 ( n - 1) d1-2 ns 2
(C)
( n - 1) f 0-14 ( n - 1) d1-2 ns 2
(D)
(D)
[ Xe ] 4f 2 5d o
(C)
[ Xe]
6s2
5d 2 6s 2
(B)
[ Xe]
4f 1 5d1 6s 2
(D)
[ Xe]
4f 2 5d1 6s1
[ Xe ] 4f 0-14 5d 0-1 6s 2
(B)
(C)
(D)
[Ra ] 5f 0-14
6d 0-1 7s 2
(B)
[Rn ] 5f 1-14
(C)
(D)
56
6d 0 - 2 7s 2
La
66.
67.
68.
(A)
69.
70.
71.
72.
73.
74.
75.
76.
C om busting in O
What is x
Ln O 3
(B)
X2
(C)
Ln 2 O
Ln 2 O 3
(D)
Ln 2 O 3
d xy @ d y 2 @ d xz < d x 2 - y 2 @ d z 2
(B)
d x 2 - y 2 @ d z 2 < d xy @ d yz @ d xy
(C)
d xy @ d z 2 < d yz @ d xz @ d x 2 - y 2
(D)
d x 2 - y 2 @ d xz < d xy @ d yz @ d z 2
77.
78.
79.
Why do theoritical value of magnetic moment differ from their practical value ?
(A) Due to decrease in volume of metal ion.
(B) Due to unsymmetrical arrangement of dipoles in orbital.
(C) Due to rotation-orbital combination.
(D) Both are different methods to calculate magnetic moment.
What is the value of magnetic moment of central metal ion in K2MnO4 ?
(A) 0.0 BM
(B) 1.73 BM
(C) 2.83 BB
(D) 3.87 BM
Which of group of ions has coloured ions ? [PMT-2001]
(1)
80.
81.
Cu 2 +
(2)
(3)
Ti 4+
(4)
Co 2+
Fe 2+
(A) 1, 2, 3, 4
(B) 3, 4
(C) 2, 3
(D) 1, 2
Which of following pair of elements has (n-1)d10 ns2 electronic configuration ? [Pb CET-1996]
(A) Fe, Co, Ni
(B) Cu, Ag, Au
(C) Zn, Cd, Hg
(D) Sc, Y, La
Which is correct increasing order of ionic radii of Ce3+, La3+, Pm3+, Yb3+ ? [AIEEE-2002]
(A)
(B)
(C)
La 3+ = Ce 3+ < Pm 3+ < Yb 3+
(D)
82.
The atomic no. of V, Cr, Mn and Fe are 23, 24, 25 & 26 respectively. Which of following has
highest value of their second ionization enthalpy ? [AIEEE-2003]
(A) V
(B) Cr
(C) Mn
(D) Fe
83.
If the radius of La3+ is 1.06 A , than what will be the approximate value of radius of Lu3+ from the
following ? [AIEEE-2003]
(A) 1.40A
84.
85.
86.
(B)
(C)
1.40A
0.85 A
(D)
1.60 A
58
87.
88.
89.
90.
(B)
(C)
(D)
(A)
(B)
(C)
(D)
>
Fe (CN )6
4-
>
[CoCl4 ]2-
The canthanide contraction is responsible for the fact that ................. [AIEEE-2005]
(A)
(B)
(C)
(D)
91.
92.
(A)
Ti 3+ , V 2+ , Cr 3+ Mn 4+
(B)
Ti + , V 4+ , Cr 6+ Mn 7 +
(C)
Ti 4+ , V 3+ , Cr 2+ Mn 3+
(D)
Ti 2+ , V 3+ , Cr 4+ Mn 5+
The appreciable shilding on outer electrons by 4f electrons from the nuclear charge.
(B)
The appreciable shilding on outer electrons by 5d electrons from the nuclear charge.
(C)
(D)
The poor shilding on outer electrons by 4f electrons from the nucluear charge.
The actinides exhibit more number of oxidation states in general than the lanthanide, because..........
[AIEEE-2007, 2008, PMT-2005, 2006]
(A)
(B)
Energy differnce between 5f and 6d orbitals is less than that of 4f and 5d orbitals.
(C)
Energy difference between 5f and 6d orbital is more than that of 4f and 5d orbitals.
(D)
59
93.
94.
95.
96.
The general oxidation state of Lanthanide elements is +3. Which of following is incorrect statement
for them ? [AIEEE-2009]
(A)
(B)
Because of the large size of the Ln (III) ions, the bonding in its compounds is ionic in character.
(C)
(D)
Once the d5 configuration nis exceeded the tendency to involve all the 3d electrons in bonding
decreases.
(B)
In addition to the normal oxidation states, the zero oxidation state is also shown by these
elements in complexes.
(C)
(D)
In the highest oxidation states of the first five (transition elements (Sc to Mn) all the 4s & 3d
electrons are used for bonding ?
(B)
In lanthanide series, ionic radius decreases while moving Ce3+ to Lu3+ ion.
(C)
(D)
In which of the following pairs are both the ions coloured in aqueous solution ? [PMT-2006]
[Atomic No. SC=21, Ti=22, Co=27, Ni=28, Cu=29]
97.
(A)
Ni2+, Cu+
(B)
Ni2+, Ti3+
(C)
SC3+, Ti3+
(D)
SC3+, CO2+
98.
22
V 3+
(B)
22
Ti 3+
(C)
25
Mn 3+
(D)
24
Cr 3+
In which of the following outer most orbit will show maximum number of oxidation states ?
[PMT-2009]
99.
(A)
3d5 4s2
(B)
3d2 4s2
(C)
3d3 4s2
(D)
3d5 4s1
Mention the colourless pair from [ Ti F6 ]2- , [Co F6 ]3- , Cu2 Cl2 & [NiCl4 2-]
[PMT-2009]
(A)
Cl2
(B)
(C)
(D)
Fe, Cr, Ni
(B)
Aq, Cu, Au
(C)
Cu, Zn, Ni
(D)
Cu, Zn, Sn
60
]2-
Mn 2+ > V 2+ > Cr 2+
(B)
V 2+ > Cr 2+ > Mn 2+
(C)
Mn 2+ > Cr 2+ > V 2+
(D)
Cr 2+ > V 2+ > Mn 2+
109. Which of following is proper reason for stability of Gd3+ ion. (Tamilnadu-CET-2002)
(A) 4f orbital is completely filled
(B) 4f orbital is half filled
(C) show electronic configuration similar to inert gas.
(D) 4f orbital is completely vacant
110. Which of ion can not show d-d transition ? (Gujarat-2007)
(A) Ti4+
(B) Cr3+
(C) Mn2+
(D) Cu2+
111. Which of following electronic configuration can show highest oxidation state ? (Gujarat-2007)
(A)
(n - 1) d 5
ns 2
(B)
(n - 1) d 8
ns 2
(C)
(n - 1) d 5
ns1
(D)
(n - 1) d 3
ns 2
(B)
(C)
(D)
118. Lanthanide contraction is observed due to increase in.............. [Kerala MEE 2003]
(A) Atomic radii
(B) Volume of 4f orbital
(C) Effective nuclear charge
(D) Atomic number
119. In................. elements, atomic volume decrease with increase in atomic number. [AIEEE-2003]
(A) p-Block
(B) f-Block
(C) Radioactive series
(D) Super heavy elements
120. Which of aqueous solution is coloured ?
[IIT-1990]
(A) Zn (NO3)2
(B) LiNO3
(C) Co (NO3)2
(D) Potash Alum
KEY NOTE
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
C
A
B
C
C
A
D
B
A
B
C
D
A
B
C
D
B
D
C
A
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
B
D
B
C
B
B
B
D
B
A
D
C
A
A
D
B
B
D
B
A
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
D
A
B
B
C
A
C
C
A
C
C
A
D
C
B
D
B
B
A
A
62
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
A
D
B
C
D
A
B
C
A
B
A
C
D
B
D
A
C
B
B
C
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
D
B
C
C
A
A
A
A
B
D
D
B
B
C
A
B
D
A
A
C
101
102
103
104
105
106
107
108
109
110
111
112
113
114
115
116
117
118
119
120
C
D
D
B
C
A
B
C
B
A
A
A
D
A
C
D
C
C
B
C
The salt that is obtained when two or more salts having independent existence combine according to
the laws of combination and which maintain the properties of original salts is called double salt e.g.
Alum is a double salt.
Similarly, the compound that is obtained when two or more salts having independent existence combine
according to laws of chemical combination and compound having new properties, formed is called
complex compound. e.g. K3[Fe(CN)6] is a complex salt.
Most of the complex compounds are formed by elements of d-block (transition elements). In the
electronic configuration of these elements, there is successive arrangement of electrons in d-orbitals.
when the atom or ion of transition elements has vacant (n1)d, ns and np or ns, np and nd orbitals,
these transition elements accept negative ions or neutral molecules and they form the compounds
which are called complex compounds. In this type of compounds, the bond that is formed between
metal ions of elements and the negative ion or neutral molecules is called co-ordinate covalent bond.
Around the centre of the metal ions of the molecules of these compounds, the negative ions or neutral
molecules are combined with co-ordinate covalent bond.
Alfred Werner, first of all gave the theory for complex compounds which is known as Werner's coordination theory. Some metals have the secondary valency in addition to their primary valence. By
this the ions of that metal combine strongly with the negative ion or neutral molecules in first attraction
sphere [ ].
According to Werner's theory, the metal ion possesses two types of valencies : Primary valency and
secondary valency.
The primary valency of the metal is equal to its oxidation number or equal to the positive electric
charge of the positive ion, which forms ionic bond, so that it gets ionized. The negative ion combines
with primary valency.
The secondary valency depends on the vacant orbitals in metal ion. The secondary valency is satisfied
by negative ions or neutral molecules. It does not get ionized. The secondary valency mentions its coordination number. The secondary valency is fixed for the metal ion but now, it has been proved that
the transition metal ions possess more than one co-ordination number. As the secondary valence being
directional determines the geometrical shape of complex compound. From the magnetic properties
also the shape of complex can be determined. e.g. In [Cr(NH3)6]Cl3, Cr is metal ion and six molecules
of neutral molecule ammonia (NH3) are combined with it by secondary valency which do not get
ionized. Hence, the co-ordination number is six. Three Cl are combined by primary valency which
gets ionized. Hence the primary valency of Cr is three.
63
Ligand is an ion having negative electric charge or neutral molecule. The classification of ligand is
made on the basis of the number of electron pair donating atoms.
If the negative ion or neutral molecule in the ligand forms one co-ordinate covalent bond by giving one
electron pair to metal ion, then it is called unidentate ligand. Neutral molecules like H2O, NH3, CO,
NO and negative ions like Cl, Br, CN act as unidentate ligands.
The ligand which donates two electron pairs to metal ion, and form two co-ordinate covalent bonds
is called didentate ligand. e.g. ethane 1,2-diamine (en), neutral and SO 24 - , CO32 - negative ions act as
didentate ligands.
The ligand in which three co-ordinate sites are indicated then it is called tridentate. In this type of
ligand the atoms donate three pairs of electrons to metal ion and form three co-ordinate covalent
bonds. e.g. Propane-1, 2, 3-triamine (ptn) neutral and PO34- , AsO34- act as negative tridentate ligand.
Six atoms in EDTA, (ethylene diaminetetracetate) ion, the six atoms donate six electron pairs and form
six co-ordinate covalent bonds, which act as hexadentate ligand.
Generally, the ligand in which two or more than two co-ordination sites are indicated, or the ligand in
which two or more than two atoms form co-ordinate covalent bonds by donating electron pairs to
metal ion is called polydenate ligand, which combines with metal ion and form complex compounds.
They are called chelate compounds which are cyclic and possess higher stablity.
The basic requirements for formation of complex compounds are ligand which can easily donate
electron pairs, there must be vacant d-orbitals in the metal ion to accept electron pairs and the metal
ion should have the symmetry same as that of the ligand.
The ion satisfying these basic requirements can easily form complex compounds.
The strength of formation of co-ordinate covalent bonds of different ligands being different, the
stronger ligand possesses more attraction towards metal ion and form strong coordinate covalent bond.
As a result, the stability of complex having strong ligand is more and the weak ligand containing
complex compounds have less stability e.g. The strength of [Ni(CN)4]2 is more than that of [NiCl4]2 .
A complex compound, in which different types of ligands combine with metal ion and form complex
compound, is called mixed ligand complex. If in any of the complex compounds only one metal ion
is present, then it is called unicentred complex compound. If in any complex compound, more than one
metal ions are present then it is called polycentred complex compound. In such unicentred or polycentred
complex compounds, the three dimensional arrangement of ligand, the different geometrical structures
are produced in co-ordination compounds, it is called polyhedra. Mostly the geometrical structures are
of shapes-tetrahedral square planar, octahedral square pyramidal, trigonal bipyramidal. To understand
these geometrical structures, the hybridization of orbitals of metal ion and magnetic properties are very
useful. sp3 hybridisation, dsp2 hybridisation, d3s hybridization in metal ions of co-ordination number four
is seen. In sp3d2 hybridization and d2sp3 hybridization, the metal ions of transition elements is seen in
64
metal ions having co-ordination number six. The metal ions of transition elements, magnetic moments of
complex compounds of ions, their geometrical structures, types of ligands etc. are described.
The nomenclature of complex compounds keeping in mind the rules of IUPAC is carried out. In
complex compounds the rules are applicable.
In nomenclature in co-ordination sphere, the name of the ligand according to English alphabets are
first mentioned. Then the name of metal is written. The suffix "O" is attached after the name of
negatively charged ligand. The name of the neutral ligand is mentioned as its original name. If the
number of same ligand is more than the one the prefixes di, tri, tetraetc. are applied. In the prefix
of organic ligand, the prefix is a mumber then the ligand is placed in bracket and the prefix bis, tris,
are attached. If the complex is negative ion then the name of ligand is written first and, in the end
the suffix 'ate' is applied to the metal ion. Its oxidation state is shown in Roman number in bracket.
If the complex is positive ion or neutral molecule, then successively writing the name of ligand, the
name of metal is added at the end and oxidation state is shown in the Roman number.
The geometry of complex compounds and magnetic properties of the complex depends on the hybridization in it. In complexes having co-ordination number 6 if strong ligand is attached with metal ion
in complex, the oxidation state is shown in Roman numbers.
In complex compounds, the geometrical structures are dependent on hybridization in it. In complex
having co-ordination number 4, if the strong ligand is combined with metal ion then dsp2 hybridization
takes place in the complex and the structure is square planar. The example of this are [Ni(CN)4]2
, [Ni(NH3 )4]2+ etc. If the co-ordination number is 4 in the complex, and the weak ligand combines
with the metal ion then sp3 hybridization takes place e.g. [NiF4]2, [Ni(H2O)4 ]2+, etc. If the coordination number in complex ion is six, and the strong ligand is combined with metal ion, then d2sp 3
hybridization and if weak ligand is combined with metal ion, then sp3d2 hybridization takes place, e.g.
In [Cr(NH3)6]3+, [Fe(CN)6]4, [Co(NH3)6]3+ d2sp3 hybridization is there, while in [FeF6]4, [Fe(H2O)6]2+
sp3d2 hybridization is there. In MnO 4- and CrO 24 - there is d3s hybridization, there are no unpaired
electrons in d-orbital due to Mn7+ and Cr6+ oxidation states; but d-d transition takes place by electrons
of ligand, and so it becomes coloured.
Three types of isomerism are observed in complex compounds-geometrical isomerism, optical isomerism and structural isomerism.
In geometrical isomerism, complex compounds having co-ordination number four- ML2A2 type, cis and
trans isomerism is observed. In complex compounds having co-ordination
type, cis and trans while in ML3A3 facial and meridional isomerism are observed. In optical isomerism,
leavo and dextro isomers are observed.
In structural isomerism, ionic isomerism, hydration isomerism, co-ordination number isomerism and
linkage isomerism are observed.
65
In formation of co-ordination compounds the magnetic nature and structural formation with the help
of valence bond theory; it has limitations. It does not produce more hindrance in magnetic property
and can not explain about the colour in co-ordination compounds. It can not give the magnitude of
hindrance in thermodynamical stability of co-ordination compounds, also it is not able to detect the
difference between weak and strong ligand. To overcome these limitations the crystal field theory
(CFT) was presented.
Crystal field theory is known as electrostatic model in which it is believed that there is ionic bond
between metal ion and ligand. According to this theory negatively charged ligand or neutral molecule
forms ionic bond. In free metal atom in gaseous state, all the five types of d-orbitals are of equal
energy (degenerate) but when ligands are arranged around the metal atom or ion in the complex, the
d-orbitals do not remain of equal energy but get splitted. The splitting of orbitals depends on the nature
of the crystal field.
The crystal field splitting (D0) depends on the field produced by electric charge of metal ion and the
ligand. Some ligands produce strong field and so splitting is in more proportion. Some ligands produce
weak field, so that the splitting is in less proportion. The series of ligands on the basis of the strength
of the field produced by ligand can be shown as below :
I < Br < SCN < Cl < S2 < F < OH < C 2 O 24- < H2O < NCS < EDTA
A < NH3 < en <
NO 2 < CN < CO : Spectrochemical series.
Metal complexes have large magnitude of colours. When the white light passes through the sample,
then it forms a specific visible spectrum and the remaining colours of white light are removed. The
absorption of colour by complex compounds is dependent on wavelength. If green colour is absorbed
then it appears of red colour.
The colour of co-ordination compounds can be explained on the basis of crystal field theory e.g.
[Ti(H2O)6] 3+ violet colour, [Ni(H2O)6] 2+ green colour, and [Ni(en)3]2+ violet colour,
Co-ordination compounds have great importance. They have immense utility value in nutrition of
minerals in plants and animals, analytical chemistry, metallurgy, biological systems and industries. They
are also used in various drugs.
66
M.C.Q.
1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
12.
13.
14.
15.
16.
67
17.
18.
19.
20.
21.
22.
23.
24.
25.
26.
27.
28.
29.
30.
68
31.
32.
33.
(C) [ZnCl4]2-
(D) [Cu(NH3)4]2+
ex-
34.
(B) 3
(C) 4
(D) 6
36.
Geometrical shapes of the complexes formed by the reaction of Ni2+ with CI-,CN - and H2O
respectively are
(A) Octahedral, tetrahedral and square planer
37.
38.
39.
(D) [Ni(CN)4]2-
(B) 2.84
(C) 4.90
(D) 5.92
(D) Linear
43.
(B) [NiCI4]2-
The spin only magnetic moment value (in Bohr magneton units) of Cr(CO)6 is
(A) Tetrahedral
42.
(D) 1.41 BM
Among the ligands NH3,en,CN and CO the correct order of their increasing field strength, is
(A) 0
41.
(C) 2.82 BM
(A) Ni(CO)4
40.
(B) 5.46 BM
(C) dz2,dxz
(B) [FeF6]3+
(C) [Co(C2O4)3]369
(D) [CoF6]3-
44.
45.
46.
47.
48.
49.
50.
51.
52.
53.
54.
55.
56.
In which of the following octahedral complexes of Co (at. no.27) will be magnitude of D 0 be the
highest ?
(A) [Co(CN)6]3(B) [Co(C2O 4)3]3(C) [Co(H2O)6]3+
(D) [Co(NH3)6]3+
The number of unpaired electrons calculated in [Co(NH3)6]3+ and [Co(F6)]3- are
(A) 4 and 4
(B) 0 and 2
(C) 2 and 4
(D) 0 and 4
In the grignard
reaction, which metal forms an organometallic bond ?
(A) Sodium
(B) Titanium
(C) Magnesium
(D) Palladium
The p - bonded organometallic compound which has ethane as one of its component is
(A) Zeises salt
(B) Ferrocene
(C) Dibenzene chromium (D) Tetraethyl tin
Which one of the following complex is an outer orbital complex ?
(At. no. Mn=25, Fe=24, Co=27, Ni=28)
(A) [Fe(CN)6]4(B) [Mn(CN)6]4(C) [Co(NH3)6]3+
(D) [Ni(NH3)6]2+
The magnetic moment of [Co(NH3)6]CI3 is
(A) 1.73
(B) 2.83
(C) 6.6
(D) Zero
In Fe(CO)5 the Fe - C bond possesses
(A) p - character only
(B)both s and p - character
(C) ionic character
(D) s - character only
According to werners theory :
(A) Primary Valeccy can be ionized
(B) Secondary valency can be ionized
(C) Primary and secondary valencies cannot be ionized
(D) Only primary valency cannot be ionized
Ligand in a complex salt are :
(A) Anions linked by coordinate bonds to a central metal atom or ion
(B) Cation linked by coordinate bonds to a central metal atom or ion
(C) Moleculer linked by coordinate bonds to a central metal atom or ion
(D) Ions or molecules linked by coordinate bonds to a central metal atom or ion
According to Lewis the ligand are :
(A) Acidic in nature
(B) Basic in nature
(C) Neither acidic nore basic
(D) some are acidic and other are basic
Which of the following acts as a bidentate ligand in complex formation ?
(A) Acetate
(B) oxalate
(C) Thiocyanate
(D) EDTA
The coordination number of cobalt in the complex [Co(en)2Br2]cl2 ?
(A) 2
(B) 6
(C) 5
(D) 4
Which is the example of hexadentate ligand ?
(A) 2,2-dipyridyl
(B) Dimethyl glyoxime
(C) Aminodiacetate ion
(D) Ethylene diammine tetra actate ion
70
57.
58.
59.
60.
61.
62.
63.
64.
65.
66.
67.
68.
69.
70.
71.
72.
73.
74.
75.
(B) [CuCl2(O=C(NH2)2)2]
(D) [CuCl2(O=C(NH2)2H2]
76.
77.
78.
80.
(A) Na 4[Fe(CN)5NOS]
(B) Na 2[Fe(CN)5NO]
(C) NaFe[Fe(CN)6]
(D) Na 2[Fe(CN)6NO 2]
83.
85.
(C) VI
(D) III
(C) [Cr(NH3)2Cl3
(D) [ Cr(en)2Cl2]
(C) +1
(D) +2
The pair of the compounds in which both the metals are in the highest possible oxidation state is ?
(A) [Fe(CN)6]3-, [Co(CN)6]3-
The number of unpaired electrons in the complex ion [CoF6]-3 is (Atomic no of Co=27)
(A) zero
84.
(B) IV
(A) -1
82.
(D) [Ag(NH2)2]Cl
(A) [ Pt(NH3)2Cl2]
81.
(C) [Ag(NH3)2]Cl
(A) II
79.
(B) Ag(NH2)Cl
(B) 2
(C) 3
(B) [Co(en)2Cl2]Cl
(D) [Pt(NH3)2Cl2]
(B) [Co(en)2Cl2]
(D) [Cr(en)2Cl2]
72
(D) 4
86.
87.
88.
89.
90.
92.
(A) [ Cr (NH3)6]Cl3
(C) [Cr(en)2Cl2]
(D) [Cr(en)3Cl3]
(A) [ Cr (H2O)6]+3
(B) [Fe(H2O)6]+2
(C) [ Cu (H2O)6]2+
96.
97.
(C) K4[Fe(CN)6]
(D) [Cu(NH3)4] SO 4
99.
(D) Polymerisation
(C) 2.23
(D) 2.38
(D) [NiCl4]2
(C) Three
(D) Five
98.
(C) Ionisation
(A) K2[PtCl6]
(A) zero
95.
(B) Linkage
Pick out from the following complex compounds,a poor electrolytic conductor in solution ?
(D) Optical
Among the following ions which one has the highest paramagnetism ?
(A) 1.414
93.
(C) Ionisation
(A) Optical
91.
(B) Geometrical
(B) Red
(C)Violet
(D) Green
(C) Triangularbipyramidal
(D) Octrahydra
(B) sp3d 2
(C) sp 3
73
(D) dsp2
100. One mole of the complex compound Co(NH3)5 Cl3 gives 3 moles of ions on dissolution in
water.one mole of the same complex react with two moles of AgNO3 solution to yeild two moles
of AgCl(s) the structure of the complex is...
(A) [Co(NH3)5 Cl]Cl2
101.
102.
103.
104.
105.
106.
107.
108.
(B) [Co(NH3)3Cl3]Z NH 3
109. In the process of extraction of gold, Roasted gold ore +CN + H2O X +OH
[X] +Zn Y + Au Identify the complexes [X] and [Y]
(A) X = [Au(CN)2]Y = [Zn(CN)4]2(B) X = [Au(CN)4]3- Y = [Zn(CN)4]-2
(C) X = [Au(CN)2]Y = [Zn(CN)6]-4
(D) X = [Au(CN)4]Y = [Zn(CN)4]-2
110. Which of the following statement is incorrect ?
(A) In K3[Fe(CN)6], the ligand has satisfied both primary and secondary valencies of ferric ion
(B) In K4[Fe(CN)6], the ligand has satisfied both primary and secondary valencies of ferrous ion
(C) In K3[Fe(CN)6], the ligand has satisfied only secondary valencies of ferric ion
(D) K4[Fe(CN)6] is diamegenetic while K3[Fe(CN)6] is paramagnetic
Assertion and Reason
Read the assertion and reason carefully to mark the correct option out of the option given below :
(A) If both assertion and reason are true and the reason is the correct explanation of the
assertion.
74
(B)
If both a ssertion and reason are true but reason is not the correct explanation of the
assertion.
(C) If assertion is true but reason is false.
(D) If the assertion and reason both are false.
(E) If the assertion is false but reason is true.
(111) Assertion : Potassium ferrocyanide and potassium ferricyanide both are diamagnetic.
Reason
: Both have unpaired election.
(112) Assertion : The [Ni(en)3]Cl2 has lower stability than (Ni(NH3)6]Cl2
Reason
: In [Ni(en)3]Cl2 the geometry of Ni is trigonal bipyramidal.
(113) Assertion : Geometrical isomerism is also called cis - trans isomerism.
Reason
: tetrahedral complexes show geometrical isomerism.
(114) Assertion : H2N - NH2 is a chelating ligand.
Reason
: A chelating ligand must possess two or more lone pair at such distance that it may form
suitable strain free ring at the metal ion.
(115) Assertion : [Ti(H2O)6]+3 is coloured while [Sc(H2O)6]+3 is Colourless
Reason
: d-d transition is not possible in [Sc(H2O)6]+3
(116) Asserion : All the octahedral complexes of Ni+2 must be outer orbital complexes.
Reason
: Outer orbital octahedral complexes are given by weak ligand.
ANSWER KEY
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
a
c
b
c
b
b
b
c
c
b
c
c
c
a
a
b
c
b
c
c
c
c
c
a
c
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
b
b
c
a
b
b
b
a
a
b
c
c
b
b
a
b
a
a
a
d
c
a
d
d
b
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
a
d
b
b
b
b
b
c
a
d
d
b
b
b
d
a
b
d
a
d
c
b
a
b
c
75
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
b
a
b
c
b
b
b
d
c
a
c
c
b
b
b
b
b
d
a
d
a
a
b
b
a
101
102
103
104
105
106
107
108
109
110
111
112
113
114
115
116
b
a
a
c
d
a
b
c
a
c
d
c
c
e
a
b
M.C.Q.
1.
2.
3.
6.
(b) S Faecalis
(d) S aurous
5.
Which of the following bacteria are responsible for the Gastrointestinal Disease ?
(a) Ecoli
4.
(b) 70 ppb
(c) 50 ppb
(d) 60 ppb
7.
Which of the following disease increase due to Green house Gases effect ?
(a) Malaria
8.
13.
(b) SOx
(c) CFC
(d) COx
14.
Which of the following size of particulate will cause diseases related to lungs ?
(a) 10-2 meter
12.
(b) Chamberlin
11.
10.
Which of the following chemist associate with Green house Gas effect ?
(a) Jean fowier
9.
(b) Dengue
(b) Na
(c) K
Which of the following ion is encouraging for the formation of algae in water ?
(a) SO42-
(b) PO43-
(c) ASO43-
77
(d) CO32-
15.
16.
17.
The lowest region that extends upto the height of 10 to 15 km from sea level is called ?
(a) Troposphere
(b) Stratosphere
(c) Smoke
18.
(c) CO2
(d) O3
(b) petrochemical
21.
(b) O2
Which of the following industries will be the best source of producing CO in the atmosphere ?
(a) Dyes
20.
19.
(b) NOx
(c) COx
22.
23.
(d) N2O5
(b) Air
(c) Soil
(d) Chlorine
28.
(c) NO
27.
(b) N2O
26.
(d) Thermoshpere
25.
(C) Troposhpere
24.
(b) Mesoshpere
(b) Arsenic
(c) Mercury
(d) Cadmium
DDT is _______________
(a) An antibiotic
29.
30.
31.
33.
38.
39.
42.
(d) 1000
(b)Aluminium sheet
(c) sugar
(d) Detergent
(c) sugar
(d) leather
(b) Refrigerators
In the coming years, skin realated disorders will be more common due to
(a) water pollution
(c) algle
43.
(c) 250
Which of the following industry produces the waste of phenolic compounds and suspended solids ?
(a) Smog
41.
(b) 500
(a) Carbon
40.
(a) petroleum
37.
(a) petroleum
36.
(b) Kidney
(a) 100
34.
(c) Carving
The pollutants like SOx, CO and NOx caused for the damage of :
(a) Throat
32.
(b) Building
(c) Fourier
(d) Newton
(b) Einstein
79
44.
A substance which may alter environmental constituents or cause pollution is called ...
(a) Radiator
45.
(b) Pollutant
(c) Reducer
(d) Decomposer
The percentage of total amount of CO present in atmosphere, due to forest fires is ...
(a) 63%
(b) 17%
(c) 9.5%
(d) 7.4%
46. The homosphere constituents how much percent of the total atmosphere
(a) 80%
(b) 86%
(c) 90%
(d) 99.99%
47. Acid rain is due to the increase in the concentration of which of the following in the atmoshpere ?
(a) O3 + NO2
52.
(b) O2 and N2
(c) O2 and O3
(d) O3 and N3
56.
(b) C6F16
(c) C6H6CL6
(d) C6F6
(c) Ozone
55.
(4) CH2=CH-CH=O
(a) PAN
54.
(3) CH3COOONO2
(2) NO2
Regular use of which of the following fertilizers increases the acidity of soil ?
(a) potassium nitrate
(b) Urea
(d)Ammonium Sulpate
In Antartica, ozone depletion is due to the formation of the following compound ...
(a) Acrolein
80
5
ANSWER KEY
1
16
31
46
17
32
47
18
33
48
19
34
49
20
35
50
21
36
51
22
37
52
23
38
53
24
39
54
10
25
40
55
11
26
41
56
12
27
42
13
28
43
14
29
44
15
30
45
81
Important Points
1.
2.
3.
Lassaigne test : It is a test used to detect the presence of N, S, P and X in organic compund.
1. L.S + FeSO4 + con H2SO4
N - present
S - present
violet colour
S - present
Cl - present
NH4OH
yellowish ppt.
Br - present
Sparingly soluble
in NH4OH
yellow ppt
I - present
Insoluable in
NH4OH
5. L. S + con HNO3 +
yellow ppt
P - present
ammonium molybdate
L.S = Lassagine solution. It is also called sodium fusion extract.
4.
5.
2mass of H2O100
18mass of O.C.
6.
28 vol of N2 at S.T.P.
224 mass of O.C.
7.
1.4 NV
Precentage of N (Kjeldahls method) = mass of O.C.
8.
9.
10.
62 mass of Mg 2 PO
100
2
7
222 mass of O.C
- 410
2
mass of platinum
M.C.Q.
1.
2.
(c) Distillation
(d) Hydrolysis
Which of the following is/are method (s) of checking the purity of organic
(a) Chromatography
3.
(b) Reduction
(b) Spectroscopy
compound ?
(c) Both (a) and (b) (d) Neither (a) nor (b)
The formula representing a simple ratio of atoms of different elements present in a molecule of
the substance is called
(a) Empirical formula (b) Molecular formula (c) Structural formula (d) Condensed formula
4.
What is called the purification technique based on difference in the solubilities of the
compound
and the impurities in a given solvent ?
(a) Sublimation
(b) CH 2
(c) C3H 2
(d) C3H 4
7.
(c) Distillation
6.
(b) Crystallization
(b) C2H4O 2
(c) C2H4O
Wh at is th e
(d) CH2O
(b) CH 3
(c) CH2O
83
(d) C2H2O 2
8.
9.
10.
Which method of purification of organic compound is useful to separate volatile liquids from
non volatile impurities ?
(a) sublimation
(b) Distillation
(c) crystallisation
11.
(b) C2H4N 2
(c) C12H24N12
(d) C16H32N16
(b) Crystallisation
(c) Sublimation
(b) 470
(c) 560
(d) 940
15.
(d) Crystallisation
14.
(c) Filtration
13.
(b) Distillation
An organic compound on analysis gave C = 48gm, H = 8gm and N = 56gm. Volume of 1.0
gm
of the compound was found to be 200 ml at STP. What is the
molecular formula of the
compound ?
(a) C4H8N 4
12.
(b) Carbon
(c) Hydrogen
(d) Halogen
16.
17.
18.
(b) 71.7
(c) 46.2
(d) 80.5
(b) SO 2
(c) H2S
84
(d) SO 3
19.
20.
21.
22.
23.
Which of the following techniques is used to separate glycerol from spent-lye in soap
industry ?
(a) Simple distillation
(c) sublimation
Chromatography is used
(a) to separate mixtures
In chromatography Rf means
(a) Retardation factor
Statements regarding Chromatography are given below. Identify True or False statements and
give your answer.
(1) Silica - gel is used as adsorbent in TLC. (2) Rf = Retardation factor.
24.
(a) TTFF
(c) TFFT
(b) Ca(OH)2
(c) CuSO4
(b) Ca(OH)2
(c) CuSO4
(b) S
(c) P
(c) X
29.
(d) glucose
28.
(c) hydrocarbons
27.
(b) ethers
26.
(d) TFTF
25.
(b) TTTT
(b) P
30.
(b) Fe4[Fe(CN)6]
(c) CuSO4
85
(d) FeSO4
31
In the Lassaigne test of detection of Sulphur, black precipitates are obtained. These are due
to the formation of
(a) Na2S
32
(b) (CH3COO)2Pb
(b) Violet
1.4 NV
W
(d) O2
NV
1.8
1.4VW
N
(c) % N =
(d) % N =
1.4 NW
V
(c) C3H4O
(d) C4H8O
(c) C2H5N
(d) C2H6N
(c) C2H4O 2
(d) CH4O
(c) C2H4O
(d) C2H8O 2
42.
(b) % N =
(b) C2H4O
(a) CH2O
41.
(c) CuO
(a) CH2O
40.
(d) O2
(a) C2H5N 2
39.
(c) CuO
(b) An.CaCl2
(a) CH3O
38.
(d) K4[Fe(CN)6]
(a) % N =
37.
(a) KOH
36
(d) Brown
35
(c) Blue
co mp ou nd is
In a Lassaigne test of Sluphur containing compound the violet colour is due to the
(a) [Fe(CN)5NO]2-
34
(d) CH3COOH
33
(c) PbS
(b) 182
(c) 17.5
(d) 175
12 m 100
44 V
(b) %C =
12 m2 100
44 m1
2 m2 100
18 m1
(d) % N =
28 V 100
22400 m
(c) % H =
86
43.
44.
(c) NO x
28 V 100
(b) 22400 m
14 V 100
(c) 22400 m
14 m 100
(d) 22400 v
(c) 34.5%
(d) 25 %
In Kjeldahls method, when nitrogenous organic compound is heated with con. sulphuric acid,
the nitrogen is converted into
(a) (NH4)2 SO 4
51.
(b) O2
(a) 20.8 %
50.
28 m 100
(a) 22400 v
49.
(c) CO 2
In Dumas method the gaseous mixture produced is passed through KOH(aq ). As a result of
this
_______ is absorbed in KOH(aq).
(b) Kjeldahlis method (c) Both (A) & (B) (d) Neither(a) nor (b).
(b)CuO
(a) CO 2
47.
(d) 21, 19
In the Dumas method nitrogen containing organic compound is first heated with
(a) O2
46.
(c) 19, 21
45.
0.1014 g H2O.
(b) NH4OH
(c) NH 3
(d) None
(a)
(b)
N:
(c)
N:
52.
(c)
During estimation of nitrogen present in organic compound by Kjeldahls method, the ammonia
cvolved from 0.5 gm of the compound neutralized 10 ml of 1 M H2SO4Calculate the %N in
the compound.
(a) 65
54.
(b) 28
(c) 56
(d) 30
In the estimation of halogen by Carius method, the halogen of the organic compound is
converted into
(a) Silver nitrate
55.
56.
59.
60.
61.
62.
63.
64.
(c) SO 2
(d) SO 3
(b) 14.20%
(c) 42.10%
(d) 38%
(c) Sublimation
(d) Distillation
(b) Chromotography
(b) Crystallisation
(d) Distillation
(b) Crystallisation
(d) Distillation
Which of the following compound will not give positive Lassaigne test for nitrogen ?
(b) urea
(c) ethylamine
(d) nitroethane.
66.
(b) BaSO4
(a) Hydrazine
65.
(d) 18.8%
58.
(c) 53.19%
57.
(b) 17.02%
(b) Sublimation
(c) Distillation
(d) None
The fragrance of flower is due to the presence of some steam volatile organic compounds
called essential oils. These are generally insoluble in water at room temperature but are
miscible with water vapour. A suitable method for the extraction of these oils from the flower
is,
(a) Distillation
(c) Crystallisation
67.
68.
69.
70.
72.
73.
75.
(c) Sublimation
What conclusion can be drawn if red colour is obtained during Lassaigne test ?
(a) Pressure of S
(b) Pressure of N
77.
78.
(b) Fe3[Fe(CN)6]4
(c) Fe4[Fe(CN)6]
(d) Fe3[Fe(CN)6]
Two volatile liquids A and B differint their boiling points by 15K. Which process can be used
for their sepration ?
(a) Fractional distillation
The ammonia evolved from the treatment of 0.3gm of organic compound for estimation of
nitrogen was passed in 100ml of 0.1m H2SO4. The excess acid required 20ml 0.5 M NaOH
for complete neutralisation The organic compound is...
(b) benzamide
(c) urea
(d) thiourea
Which of the following compound gives blood red colouration when its Lassaigne extract is
treated with alkali and ferric chloride ?
(a) Thiourea
(d) Benzomide
Which of the following compounds will give Lassaigne test for nitrogen ?
(a) NH2NH 2
76.
(a) Crystallisation
(a) acetamide
74.
(c) a and B
Name the method used to separate a mixture of iodine and sodium chloride ?
(a) Fe4[Fe(CN)6]3
71.
(b) RNA
(b) NaNO3
(c) NH4Cl
(d) NaCN
Which of the folowing will give bloodred colour while doing Lassaigne test for nitrogen
(a) urea
(c) Hydrazine
Name the method used to determine the molecular weight of organic compound.
(a) Silver salt method
While detecting phosphorous in organic compound yellow colour is obtained due to the
formation of
(a) (NH4)2MoO4
(b) (NH4)3PO 4
(c) (NH4)3PO 4 . 12MoO3 (d) MgNH4PO 4
89
79.
0.306 gm of the silver salt of a monobasic organic acid yeilds 0.216gm of Silver on ignition.
Find molecular weight of the acid.
(a) 46
80.
(b) 23
(b) 192
(b) 91.45
84.
85.
(c) Cl /hv
(b) C H O & C H O
91.
12
22
11
12
12
22
11
12
An organic compound having molecular mass 60 is found to contain C=20%, H=6.67% and
N=46.67% while rest is oxygen. On heating it gives NH along with a solid residue. The solid
3
residue give violet colour with alkaline CuSO , the compound is
3
(b) CH CONH
3
(c) (NH ) CO
2 2
(d) CH CH CONH
3
(c) Distillation
(d) Crystallisation
When 32.25 gm ehtyl chloride dehydrohalogenated it gives 50% alkene. What is the mass of
product ?
(b) 14 gm
(c) 21 gm
(d) 28gm
How much sulphur is present in organic compound if on analysis 0.53gm of this compound
gives 1.158gm of BaSO ?
(a) 10%
90.
(a) 7 gm
89.
(c) gases
(a) Sublimation
88.
(d) 410
(a) CH NCO
87.
(c) 98
(b) liquids
86.
(d) 234
83.
(c) 208
0.3557gm of the Platinum salt of monoacidic organic base yeilds 0.117gm of platinum. Find
molecular weight of base
(a) 95
82.
(d) 20
1.026gm of the silver salt of a tribasic organic acid gave an ignition 0.648gm silver. Find
molecular
weight of the acid.
(a) 148
81.
(c) 122
(b) 20%
(c) 30%
(d) 40%
(c) Sublimation
(d) Distillation
(b) P
(c) X
90
(d) S
92.
An organic compound weighing 4.337mg yielded 10.35mg of CO2 and 3.42mg of H2O on
oxidation with CuO. Calculate the empirical formula of the compound.
(a) C3H 5
93.
94.
(c) C4H6O
An organic compound contains 69% C and 4.8% H, the remainder being oxygen. Calculate
the masses of CO2 and H 2O produced when 0.2gm of this substance is completely
combusted.
(a) 0.506g & 0.864g
95.
(b) C3H5O
(b) 40.5%
(c) 35.7%
(d) 31.23%
In the estimation of sulphur by Carius method, 0.468gm of organic compound gave 0.668gm
BaSO4. Calculate % of S.
(a) 19.6
(b) 21.7
(c) 17.9
(d) 16.9
In each of the following questions, a statement (A) is given followed by Reason (R).
Give your answers as
(A) If both A and R are true, and reason is the true explanation of the assertion.
(B) If both A and R are true, but R is not the true explanation of the A.
(C) If A is true but R isfalse.
(D) If both A and R are false.
96.
97.
A: Lassaignes extract is boiled with dil.HNO3 before testing for halogens by AgNO3.
R: CN- and S2- present in Lassaigne extract interfere with the test of halide ions by silver
nitrate.
98.
99.
100. A: Sulphur present in organic compound can be estimated quantitavely by Carius method.
R: Sulphur is separated easily from other atoms in the molecules and gets precipitated as light
yellow solid.
91
Answer Key
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
C
C
A
B
D
B
C
C
B
B
A
A
D
D
C
A
B
A
C
A
D
A
A
A
A
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
C
D
D
A
B
C
B
B
A
B
A
B
B
C
B
A
A
B
C
D
A
A
B
B
A
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
92
D
A
C
B
A
B
C
D
C
B
B
A
D
A
B
D
C
C
C
A
A
B
C
A
D
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
D
D
C
A
B
B
D
B
C
D
C
C
A
C
B
D
D
D
A
A
D
A
D
A
C
HINTS
11.
17.
%Cl =
39.
35.5 0.287
100
143.5 0.099
Elements
No. of moles
C
H
6/12 = 0.5
1/1
=1
O
8/16 = 0.5
\ E.F = CH2O
M.W = 2VD =60
\ n = 2 \ M.F = C2H4O2
%S =
49.
P = 715 - 15 = 700 mm
Vol of N 2 at STP =
273 700 50
= 41.9 ml
300 760
\ %N =
73.
1
2
1
32
0.35
100 =18.52
233 0.2595
41.
53.
Simple ratio
14 20
g nitrogen
1000
14 20 100
= 56.0%
1000 0.5
1.4 2 50 0.1
= 46.6
0.3
28
% N in urea = 100 = 46.6
60
%N =
108 0.306
- 107 = 46
0.216
79.
MW =
81.
1 195 0.3557
MW =
- 410
2 0.117
93
28 41.9 100
=17.46%
22400 0.3
Variety of organic compound are obtained by subtitution of one or more hydrogen atom of
hydrocarbon by element like nitrogen, oxygen, sulpher and halogen OR by functional group.
So, organic chemistry consists of hydrocarbon and large variety of compounds obtained from the
subsitution of their hydrogens.
Tetravalency of Carbon :
The atomic number of carbon is 6 and hence, the number of electron in carbon is 6, so the
electronic configuration is 1s2 2s2 2px1, 2py1 2pz0. Here the number of electrons in its outermost orbit
are four. In order to attain a stable electronic configuration like inert gs carbon atom should either
lose four electrons or gain four electrons. To achive this, a very large amount of energy is required.
Consequently it cannot form C4+ or C4- ion. However, the carbon atom shares four electrons with
some elements and forms four covelentbonds.
Thus a carbon atom forms four covalent bonds in its compounds. For example, a molecule of
methane (CH4) is formed when four electrons of carbon are shared with four hydrogen atoms as
shwon below :
H
x
C + 4H
H C H
or
H C H
Methane
In a similar manar carbon can complete its octet by sharing its valence electrons with the
electrons of atoms as well. This charactersitc of carbon atom by virtue of which it forms four covalent
bonds is generally referred to as tetracovalency of carbon.
Catenation : a unique property of carbon :
One of the remarkable property of carbon atom is its unique capacity to form bonds with
other carbon atoms. This property of forming bonds with atoms of the same element is called
catenation. Carbon shows maximum catenation in its group (group 14) in the periodic table. This is
because of the larger strength of carbon to carbon bond as compared to that of other atoms. For
example, C-C bond is very strong (335 kJ mol-1) in comparison to Si-Si bond (220 kJ mol-1) or
Ge-Ge bond (167 kJ mol-1). As a result, carbon atoms can link with each other to form either linear
94
E:\JEE NEET\Bhaveshbhai\07012013\ Unit 20 summary eng 1 to 11 pg
chains of various lengths of branched chains and even rings of different sizes as shown below :
2p
(Ground state)
C
(Excited state)
sp hybridisation
form four hybrid orbitals
(a)
(b)
(c)
95
2s
2p
(Ground state)
sp3 hybridisation
C
(Excited state)
Unhybridised
orbiral
For example in the case of ethylene one sp2 hybrid orbital of one carbon atom overlaps with
sp2 hybrid orbital of the other carbon atom to form C-C sigma bond. The remaining two sp2 hybrid orbitals of both the carbon atoms overlap with 1 s-orbitals of two hydrogen atoms to form
C-H sigma bonds.
The unhybridised orbital (shown dotted) participates in the formation of pi bond. The orbital
structure of ethylene has been shown in fig.______
3.
C
(Ground state)
C
(Excited state)
For example, in the case of acetylene, one sp-hybrid orbital of one carbon atom overlaps with
sp-hybridorbital of the second carbon atom and forms C-C sigma bond. The remaining sphybridorbital of each C-atom forms sigma bond with H-atom. Each of the unhybridised orbitals of
one carbon atom forms bond with the second carbon atom so that there are two bonds in acetylene
molecule. The structure of acetylene (ethyne) is shown in Fig. 12.4
97
E:\JEE NEET\Bhaveshbhai\07012013\ Unit 20 summary eng 1 to 11 pg
7.5
Sigma bonds are stronger bonds than bonds because during the formation of bond, the
overlapping of orbitals takes place to a larger extent.
Important features of Bonds : As already discussed, the double bond in ethylene molecule consists
of a bond and a bond. The bond has some important features as listed below :
1.
In ethylene, as discussed earlier, the two 2p (unhybridised) orbitals participating in the bond
are parallel to each other. For the proper sidewise overlap of these 2p-orbitals, all the atoms in
C2H4 molecule must be in same plane. Thus, the formation of bond restricts the molecule into a
plannar shape. Therefore, ethylene is a flat or planar molecule.
2.
Due to the bond formed by sidewise overlap of 2p-orbitals, the rotation of one CH2 fragment
with respect to other will be hindered. The rotation of one carbon atom throug h 900 will break the
bond because in that case, the unhybridised 2p-orbitals become perpendicular to each other and no
sidewise overlap is possible. Hence, to rotation about the double bond is restricted or hindered. As
a result, there are two distinct forms of molecules such as C2H2Cl2 as shown ahead :
Functional Groups :
An atom or group of atoms that determines the characteristic reaction of an organic compound
is known as functional group. In alkane hydrocarbons due to their saturation they do not contain
functional group for their characteristic reaction. The different compounds have the same functional
group under similar reactions.
Class of
Functional
compound group
Alkane
R-H
IUPAC
group
prefix/suffix
-/ ane
Alkane
C=C
-/ ene
Alkyne
-C = C-
-/ yne
Halide
-X
halo/(-F,-CI,-Br,-I)
Ether
-OH
alkoxy/-
Examples
TUPAC Name
CH 3-CH 3
CH3 -CH2-CH3
CH3-CH 2-CH2-CH3
CH2=CH 2
CH3CH=CH 2
CH3CH 2CH=CH2
CH3CH=CH-CH3
HC = CH
CH3-C=CH
CH3CH2C=CH
CH3C=C CH3
CH3CH2 CH2CI
CH3CH CH3
CI
CH3CHCH2 CH 2CH3
CI
CH 3 OH
CH 3CH 2OH
CH 3CH 2 CH 2OH
CH3 CHCH 2
OH
Ethane
Propane
Butane
Eshene
Propane
But-1-yne
But-2-yne
Ethyne
Propyne
But-1-ene
But-2-ene
1-Chloropropane
2-Chloropropane
98
E:\JEE NEET\Bhaveshbhai\07012013\ Unit 20 summary eng 1 to 11 pg
1-Chloropentane
Methanol
Ethanol
Propan-1-ol
Propan-2-ol
Class of
Functional
compound group
Ether
-O-
IUPAC
group
prefix/suffix
alkoxy/-
Aldehyde
-CHO
-/ al
Ketone
-CO-
-/one
Carboxylic -COOH
Acid
-/oic Acid
Estar
-COOR
-/oate
Amide
-CONH 2
-/ amide
Amine
-NH 2
(10)-/ amine
(Primary)
Nitro
Cynide
OR
Nitrile
-NH-
(2 )-/ amine
(Primary)
-N-
(30)-/amine
(Tertiary)
-NO 2
-C=N
nitro/-
-/ nitrile
Examples
TUPAC Name
CH3-O-CH 3
CH3-O-CH 2CH 3
CH3-CH2-O-CH2-CH3
HCHO
CH 3CHO
CH 3CH 2CHO
CH3 COCH 3
CH 3COCH 2CH 3
CH 3CH 2COCH 2CH 3
HCOOH
CH3 COOH
CH3 CH 2COOH
HCOOCH3
CH3 COOCH3
CH3 COOCH2CH 3
CH 3CONH 2
CH 3CH 2CONH 2
CH3 NH 2
CH 3CH 2NH 2
CH 3CH 2CH2 NH 2
Methoxy methane
Methoxy ethane
Ethoxy ethane
Methanal
Ethanal
Propanal
Propanone
Butan-1-one
Pentan-3-one
Methanoic acid
Ethanoic acid
Propanoic acid
Methyl methanoate
Methyl ethanoate
Ethyl ethanoate
Ethanamide
Propanamide
Methanamine
Ethanamine
1-Propanamine OR
Propan-1-amine
CH3CH CH3
NH 2
CH3NHCH 3
CH 3CH 2NHCH 3
CH 3
CH 3NCH 2CH 3
CH 3
CH3N CH3
CH 3CH 2NO 2
CH 3CH 2CH2 NO 2
CH3 CHCH 3
NO 2
Propan-2-amine
N-methyl methanamine
N-methyl ethanamine
N-N dimethyl ethamine
N-N dimethyl
methamine
Nitroethane
1-Nitropropane
2-Nitropropane
CH 3CN
CH 3CH 2CN
Ethane nitrile
Propane nitrile
CH 3CH 2CH 2 CN
Butane nitrile
99
E:\JEE NEET\Bhaveshbhai\07012013\ Unit 20 summary eng 1 to 11 pg
7.6
Homologus Series
A series of organic compounds having same functional group in which two successive members
differ from each other by fixed number of carbon and hydrogen (CH2). Such series of organic
compounds is known as homologus series. Almost all types of organic compounds form homologus
series and they have similar chemical characteristics e.g. CH4, C2H6, C3H6, C3H8 etc.
7.6.1. Characteristics of Homologus series :
(1) The elements and functional group present in compound of a homologus series are same.
(2) Each member of the series can be expressed by common molecular formula. For example, each
member of alkane series can be indicated by a common formula CnH2n+2.
(3) The difference between the molecular formula of two successive members of the series will be of
CH2.
(4) The difference between the molecular weights of two successive members of a series will be of 14
amu (u).
(5) The name of each member of a series begins either with a common prefix orsuffix.
(6) The chemical reactions of each member of series are same are same if the functional group present
in them is same and their methods of preparation are also the same.
(7) As the number of carbon and hydrogen atoms increase with member of a given series the molecular
mass of the members increases. Hence there will be gradual change in the properties of the members
which depend upon their molecular mass which include boliling point, melting point, density, solubility
etc. The characteristics homologous series of alkane compounds are given in table 7.2.
Characteristics of homologous series of alkanes.
Name of
Alkane
Bolling
polint0K
State
gram/mole
Methane
CH4
16
91
109
gas
Ethane
C2H6
30
87
184
gas
Propane
C3H8
44
83
231
gas
Butane
C4H10
58
135
272.5
gas
Pentane
C5H12
72
143
309
gas, liquid
7.7
Isomerism
The organic compounds having the same molecular formula but different structures are called
isomers. This phemenon is called isomerism. The isomers have been classified mainly in two types
depending upon their differences in structural aspects :
(1) Structural isomerism
(2) stereo isomerism
7.7.1. Structural Isomerism : Structural isomerism is a result of different arrangements of atoms or groups
of atoms in molecules or organic compounds having same molecular formula. Hence, the organic
compounds having same molecular formula but different structures are called structural isomers and
and phenomenon as structural isomerism. There are five different types of structural isomerism :
100
E:\JEE NEET\Bhaveshbhai\07012013\ Unit 20 summary eng 1 to 11 pg
(1) Skeletal or chain isomerism (2) Position isomerism (3) Functional group isomerism (4) Metamerism
(5) Tautomerism.
(1) Skeletal or chain isomerism : The organic compounds having same molecular formula but
arrangement of carbon atoms in a linear or branch are different ; such type of isomerism is called
chain isomerism. Methane, ethane and propane do not exhibit chain isomeism but butane has two
isomers. Pentane has three isomers, hexane has give isomers. For example three isomers of pentane
are given below.
(i)
n-pentane
CH3CH2CH2CH2CH3
(ii) 2-methyl butane
CH3CHCH2CH3
CH3
(iii)
(2) Position isomerism : Organic compounds have same molecular formula and similar carbon
chain but differ in the position of functional group. This type of isomerism is called position isomerism.
For example,
(i)
CH3CH2CH2NH2
1-Propanamine
CH3CHCH3
(ii)
NH2
CH3CH2CH2CH2CH2OH
CH2CH2CH2CHCH3
2-Propanamine
Pentan-1-ol
Pentan-2-ol
OH2
CH3CH2CHCH2CH3
OH2
Pentan-3-ol
(3) Functional group isomerism : The organic compounds having the same molecular formula but
different functional groups are called functional isomers and this phenomenon is called functional
group isomerism ; for example,
(i)
CH3CH2CH2OH
CH3-O-CH2CH3
propan-1-ol
methoxy ethane
(ii) CH3CH2CHO
CH3-CO-CH3
propanal
propanone
(iii) CH3CH2COOH
CH3-COO-CH3
propanoic acid
methyl ethanoate
101
E:\JEE NEET\Bhaveshbhai\07012013\ Unit 20 summary eng 1 to 11 pg
M.C.Q.
1.
2.
3.
(d) vanderwals
5.
(c) metallic
(b) covalent
(b) 2
(c) 3
(d) 4
(b) 2
(c) 3
(d) 4
Shape of molecules
6.
7.
(b) C2H4
(c) C2H2
(d) C4H8
(b) 139 pm
(c) 134 pm
(d) 120 pm
10.
(d) n- pentane
9.
(c) Neohexane
8.
(b) Isopentane
(b) p-orbitals
(d) sp orbitals
Look at the figure given below and select the right option.
(a) a and b are sp3 orbitals and their side wise overlapping forms two p - bonds.
(b) c and d are two p - bonds concentrated around bond axis.
(c) c and d are two electron clouds of one p - bond and it is formed by the side wise overlap
between two pz orbitals.
(d) c and d are two s - bonds formed by the lateral overlap of two pz orbitals.
11.
12.
(1) C having CH3 bond in the molecule is in sp3 hybridisation and so all the sp3 hybride orbital
and used in s - bonds.
(2) That 4C H and 2C C type bonds are present in the molecule.
(3) The molecule becomes planar triangular because of two s bonds having sp hybridization two
bonds in which bond angle is 120o.
(4) The H-C-C angle is 109o 28 because of sp3 hybridization of CH3 group in C in the whole
molecule but the other two C with it are in sp hybridation and so linear and joined by triple
bond.
(a) 1
13.
14.
15.
16.
17.
(b) 2
(c) 3
(d) 4
Hybridization
The compound in which carbon uses only its sp3 hybrid orbitals for bond formation is
(a) HCOOH
(b) (NH2)2CO
(c) (CH3)3 COH
(d) (CH3)3 CHO
The bond between carbon atom (1) and carbon atom (2) in compound N = C CH = CH2
involves the hybridised carbon as
(a) sp2 and sp2
(b) sp3 and sp
(c) sp and sp2
(d) sp and sp
2
Number of electrons in cyclobutadienyl anion (C4H4) is
(a) 2
(b) 4
(c) 6
(d) 8
Homolytic fission of C - C bond in ethane gives an intermediate in which carbon is
(a) sp3 hybridized
(b) sp2 hybridized
(c) sp hybridized
(d) sp2d hybridized
A straight chain hydrocarbon has the molecular formula C8H10. The hybridisation for the carbon
atoms from one end of the chain to the other are respectively sp3, sp2, sp2, sp3, sp2, sp2, sp
and sp. The structural formula of the hydrocarbon would be
(a) CH 3 - C C - CH 2 - CH = CH - CH = CH 2
(b) CH 3 - CH 2 - CH = CH - CH 2 - C C - CH = CH 2
(c) CH 3 - CH = CH - CH 2 - C C - CH = CH 2
(d) CH 3 - CH = CH - CH 2 - CH = CH - C CH
18.
19.
20.
21.
When the hybridization state of carbon changes from sp3 to sp2 and finally to sp, the angle
between the hybridized orbitals
(a) decreases
Match the following : (More than one option in column - II may match with single option in
column-I). Match the hybridization state of below listed carbon atoms.
CH2 = C = CH CH2 C ? C CH2 NH2
Column - I
Carbon atoms
(A) C1
(B) C2
(C) C5
(D) C6
Column - II
Hybridization state
(P) sp
(Q) sp2
(R) sp3
(S) dsp2
(a) A = R
B = P
C = Q
D= P
(b) A = P
B = P
C = Q
D =R
(c) A = R
B = P
C = S
D= P
(d) A = S
B=R
C = Q
D= P
Homologous series
22.
23.
(b) atom
(c) proton
24.
(b) 14
(c) 16
(d) 18
(b) solubility
(c) density
(d) all
27.
(d) CnH2n+2H
As number of C atom in homologus series increases Then which of the following will increases?
(a) B.P/M.P
26.
(c) CnH2nH
25.
(b) CnH2n-1H
(b) propane
(c) butane
(d) pentane
28.
In homologous series :
(a) Molecular formula is same
29.
30.
31.
32.
33.
34.
35.
36.
37.
38.
39.
40.
41.
42.
43.
44.
45.
46.
47.
48.
50.
51.
52.
53.
54.
The maximum number of structural isomers (acyclic and cyclic) possible for C4 H6 are
(a) 4
(b) 5
(c) 6
(d) 7
The structures (CH3)3 CBr and CH3(CH2)3 Br present
(a) chain isomerism
(b) position isomerism (c) functional isomerism (d) both (a) and (b)
The maximum number of isomers of an alkene with molecular formula C4H8 is
(a) 2
(b) 3
(c) 4
(d) 5
A compound which is not isomeric with diethyl ether is
(a) enantiomers
(b) diastereomers
(c) structural isomers (d) none of the above
Which of the following compounds can be optically active?
(a) propionic acid
(b) 2-chloropropionic acid
(c) 3-chloropropionic acid
(d) chloropropionic anhydride
Which one of the following can exhibit cis-trans isomerism?
(a) CH3CHClCOOH
(b) HC CCl
(c) ClCH = CHCl
(d) ClCH2CH2Cl
Compound having open chain is (A) Pentane
(B) Isopentane
(C) Neopentane
(D) All the above
In unsaturated compound have
(A) Carbon - carbon double bond
(B) Carbon - carbon tripel bond
(C) Carbon - carbon double and triple bond (D) Carbon - oxygen double bond
114
55.
56.
57.
58.
(C) Pyrrole
(A) A
(B) A
(C) A
(D) A
C
C
C
C
p,
p,
p,
p,
s,
s,
q,
s,
r, s
r,
r, s,
r, s,
D
D
D
D
q
s
p
p
(C) Two
(D) Three
(C) 6
(D) 4
The total number of secondary H-atoms in the structure given below are : (CH3)2CHCH2C2H5
(A) 1
61.
(A) 5
60.
p
p, q,
p, s,
p, q,
(A) None
59.
B
B
B
B
(D) Cyclobutane
(B) 4
(C) 3
(D) 2
iso-octane contains
(A) 5 primary. one secondary. & two tertiary. C atoms.
(B) 4 prim. 2 sec. & one ter. C atoms.
(C) 5 (1oC). one (2oC), one (3oC) & one (4oC) atoms.
(D) 4 (1oC). two (2oC), one (3oC) & one (4oC) atoms.
62.
(b) Vinylidene
(c) Benzyl
(d) Methylidyne
(A) a , d
(B) a , b , d
(C) a , b
(D) a, b, c
115
mirror\Desktop\\CHEMISTRY\Unit - 9 Chemistry Apurav (2nd Proof)
87.
88.
89.
(A)
(B)
(C)
(D)
90.
91.
92.
93.
119
mirror\Desktop\\CHEMISTRY\Unit - 9 Chemistry Apurav (2nd Proof)
94.
Write the correct IUPAC name of the following bond line formula :
96.
97.
(B) 3-bromo-1-chlorocyclohexene
(D) 2-bromo-6-chlorocycohex-1-ene
98.
(A) 6-bromo-2-chlorocyclohexene
(C) 1-bromo-3-chlorocylohexene
IUPAC name of the compound is
99.
(B) 2-Methylbutanal
(D) 2-Ethylpropanal
100.
(A) Butan-2-aldehyde
(C) 3-Methylisobutyraldehyde
The IUPAC name of the compound is :
95.
101.
102.
(B) 5-vinyloct-3-en-1-al
(D) 3-butyl-1,4-hexadien-6-al
103.
(A) 4-butyl-2,5-hexadien-1-al
(C) 5-vinyloct-5-en-8-al
The IUPAC name of is :
104.
105.
106.
121
mirror\Desktop\\CHEMISTRY\Unit - 9 Chemistry Apurav (2nd Proof)
107.
108.
(A)
(C)
109.
110.
111.
&
(B)
&
(D)
&
&
(B)
(C)
(D)
Reasoning
(A) If both Statement- I and Statement- II are true, and Statement - II is the correct explanation
of Statement I.
(B) If both Statement - I and Statement - II are true but Statement - II is not the correct
explanation of Statement I.
(C) If Statement - I is true but Statement - II is false.
(D) If Statement - I is false but Statement - II is true.
122
mirror\Desktop\\CHEMISTRY\Unit - 9 Chemistry Apurav (2nd Proof)
112.
113.
114.
115.
116.
117.
118.
119.
120.
121.
Statement
Statement
(A) A
Statement
Statement
(A) A
Statement I :
is called cyclohexancarbonitrile.
122.
123.
124.
125.
126.
127.
128.
129.
130.
(A) C6 H5CH 2 C H 2
131.
132.
133.
134.
135.
(B) C6 H5 C HCH3
(C) CH3 C H 2
(D) CH3 C HCH3
Which of the following is the most stable carbocation (carbonium ion)?
(a) CH3 CH2+
(b) (CH3)2 C+H
(c) (CH3)3 C+
(d) C6H5 C+ H2
What is the decreasing order of stability of the following ions?
(i) CH3C+HCH3 (ii) CH3C+HOCH3 and (ii) CH3C+HCOCH3
(a) i > ii > iii
(b) ii > iii > i
(c) iii > i > ii
(d) ii > i > iii
Find the no. of functional groups and no. of chiral centres respectively
(A) 5, 4
(B) 8, 3
(C) 6, 3
(D) 6, 2
Inductive effect Electromeric effect Resonance and hyperconjugation
Decreasing I power of given groups is (a) CN
(b) NO2
(c) NH2
(d) F
(A) b > a > d > c (B) b > c > d > a
(C) c > b > d > a
(D) c > b > a > d
The reaction C2H5Br + KOH ? C2H5OH + KBr is an example of
(a) free radical substitution
(b) electrophilic substitution
(c) nucleophilic substitution
(d) rearrangement reaction
124
136.
137.
138.
(d) 1, 3, butadiene
141.
Which of the following has the smallest heat of hydrogenation per mole?
(a) 1 - butene
140.
(d) CH3CH2CH3
139.
(b) hyperconjugation
142.
143.
The correct order of increasing basic nature for the bases NH3, CH3NH2 and (CH3)2NH is:
(a) CH3NH2 < NH3 < (CH3)2NH
(1)
(a) (1), (2), (3), (4)
144.
(A)
(C)
(a) 1 and 4
(B)
(b) 3 and 4
(c) 2 and 4
(d) 1 and 3
HH
(1)
146.
(4)
145.
(3) CN
H
H
H
H
(2)
(3)
H
C
H
H (4)
(B)
+
(C)
+
125
mirror\Desktop\\CHEMISTRY\Unit - 9 Chemistry Apurav (2nd Proof)
H
H
(D)
147.
148.
149.
(B) (CH 3 )3 C OH
(C) CH 3 CH 2 - OH
(D) CH 3 - CH 2 - O - CH 2 - CH 3
150.
151.
152.
(b) C2 H 5 - S - C2 H 5
(c) CH 3 - O - CH 3
(d) CH 3 - O - C2 H 5
ANSWER KEY
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
b
c
c
b
d
d
c
d
b
c
a
c
c
c
d
b
d
c
c
d
a
d
a
b
d
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
d
d
d
c
d
b
a
a
c
d
d
a
b
b
b
d
d
c
d
c
c
d
d
a
c
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
b
c
d
c
a
d
d
c
b
b
c
c
c
b
a
c
b
b
b
d
c
c
c
b
d
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
b
b
c
b
a
b
d
b
d
b
b
c
d
c
d
a
a
b
b
b
c
b
d
b
b
126
mirror\Desktop\\CHEMISTRY\Unit - 9 Chemistry Apurav (2nd Proof)
101
102
103
104
105
106
107
108
109
110
111
112
113
114
115
116
117
118
119
120
121
122
123
124
125
c
a
c
b
b
c
c
d
b
c
b
b
b
c
a
c
c
d
b
b
a
c
a
d
b
126
127
128
129
130
131
132
133
134
135
136
137
138
139
140
141
142
143
144
145
146
147
148
149
150
c
b
a
c
b
c
d
c
a
c
c
c
d
b
b
b
c
c
b
c
a
b
b
b
c
151
152
d
d
UNIT : 21 HYDROCARBONS
Important Points
Organic Compounds Containing Only Carbon and hydrogen are Called hydrocarbons. These are
Classified as follows
Hydrocarbons
Alkane
Alkene
Alkane
Arene
Cn H2n + 2
Cn H2n
Cn H2n - 2
Cn H2n - 6
C-C
C=C
C=C
Alternate
SaturatedUnsaturated
Unsaturated
C - C and C = C
specific unsaturated
Missing Points :In this Hydrocabon unit following points are in the syllabus of JEE but not discussed is GSEB Text
Book. So prepare following points.
-: Alkyne :(1)
Na / NH 3
Bireh Reduction R CH = CH2 CH OH R CH2 CH3
3
(2)
Corey-House Reaction
(3)
Franklands Reaction:-
2R X + Zn R R + ZnX2
(4)
Kolbes Electrolysis:-
R - COONa R - COO + Na +
At anode :(5)
2R - COO R - R + CO2 + 2e
D
Pyrolysis or Cracking :- C3 H8
-: Alkenes :(1)
(2)
H 2 SO4 / HgSO4
CH 3CH 2OH
CH2 = CH2 + H2O
Hydration
(3)
Cold Alk.
CH CH
Baeyer`s Test :- CH2 = CH2
2
2
KMnO
4
127
OH
OH
(4)
Hot Alk.
2H COOH
CH2 = CH2
KMnO4
-: Alkyne :(1)
/ liq NH 3
-X
HC CH Na
HC C Na a R
R - C CH + Nax
(2)
Cold Alk.
CH3 C CH CH3 COOH + CO2
Kmno4
(3)
Hot Alk.
CH3 COOH + CO2
CH3 C CH
Kmno4
(4)
HC CH + R - Mg - X R - H + HC C - MgX
-:Arene:(1)
Br
ether
+ 2Na + CH3 CH2 Br
(2)
(3)
Cr2O3 / Al2 O3
CH3 (CH2)4 CH3
770K
+ 3H2
Benzene
CH 3 - ( CH 2 )5 - CH 3
CH3
n - heptone
CH3
(4)
+ 2NaBr
Cr2O3 / Al2O3
770 K
CH3 C C H
( i ) O3
|| ||
+2
( ii ) Zn / H 2 O
O
Methye Glyoxal
CH2 CH3
(5)
Toluene
Alk KMnO
4
373 - 383K
COOH
128
CHO
|
CHO
Glyoxal
M.C.Q.
(1)
(2)
(9)
(b) Propane
(d) Propene
(b) Ethane
(c) Propane
(d) Butane
(b) n- pentane
(c) iso-Pentane
(8)
(d) C4 H6
(7)
(c) C3 H8
(6)
(b) C5 H12
(5)
(d) Ethene
If Sodium Propionate is heated with sodium propionate then what will be the product ?
(a) Ethane
(4)
(c) Butane
(3)
(b) Propane
Mg / Ether
(a) CH3CH2CH2Cl
H 2O
CH 3 Mg X
(b) CH3COCI
H 2O
B2 H 6
(d)
CH3 - CH - CH3
OH
2HI
Re d P
(10) When ethyl iodide and propyliodide react with Sodium in presence of ether they form ?
(a) Only One alkane
(b) Ethane
(c) Propane
(d) Butane
(b) C3 H8 + C4 H10
(c) C2 H4 + C2 H2
(d) C6 H6 + C6 H12
(13) Aqueous solution of the which of following compound on electrolysis gives ethane ?
(a) Sodium formate
(c) Ethanoicacid
(d) Ethylacetate
(14) As the number of branches in a chain increases the boiling point of alkane.....
(a) Increases
(b) Decreases
129
(b) Staggered(Anti)
(c) boat
(b) 9
(c) 10
(d)12
(20)
/c
C2 H5Cl + H2 Pd
(a) Ethene
(b) Ethane
(c) Ethyne
(b) Addition
(c) Pyrolysis
(d) Isomerisation
(c) C3 H8
(d) C4 H10
(b) C2 H6
(23) n- butane on reacting with bromine in presence of sun light given mainly ----(a) CH3 - CH2 - CH2 - CH2 Br
CH3 CH CH 2 Br
|
(c)
CH3
CH3
|
(d) CH3 C Br
|
CH3
(25) How many Chiral Compounds are possible on monochlorination of 2methyl butane
(a) 2
(b) 4
(c) 6
(d) 8
(26) How many moles of O 2 are required for complete combustion of one mole of propane
(a) 3
(27)
(b) 10
(c) 5
(d) 6
Zn - Cu
HCl
CH 3CH (OH )CH 3
130
(28) Methyl chloride react with Lithium diethyl Copper to give---(a) Ethane
(b) Propane
(c) Butane
(d) Propene
(29) Which of the following alkyl bromides may be used for the synthsis of 2,3-dimethyl butane by
Wurtz raection ?
(a) n- propyl bromide
(a)
CH3
CH3
(b)
(c)
Br
Br
(d)
CH3 Br
Br
(b) Addition
(c) Elimination
(d) Rearrangement
(32) When ethene treated with Br2 in presence of CCl4Which compound is formed
(a) 1, 2-dibromoethane
(b) 1-bromo-2-chloroethane
(d)1-bromo ethaen
Alcoholic
A.the product is
(33) CH3CH2 CI
KOH
(a) CH3CH2 OH
(b) CH3CHO
(34) When butane 2-ol is heated with H2 SO4 the major product is
(a) But-1-en
(b) But-2-en
KMnO4
X. In this reaction product X is
(35) CH2 = CH2
KOH/H 2 O
(a) Ethanol
(c) Ethane
(a) propane
(37)
(a)1-bromo propane
(d) propane
(38) when 3-phenyl propene reacts with HBr in the presence of peroxide, the major product form is
(a) 2-bromo-1-phenyl propane
(c) 3-(0-bromo phenyl )propane
(b) R - COOH
(c)
RCR
||
O
(d)
R CH CH R
|
|
OH OH
RCR
||
(c)
O
(d) R - CHO
(c) O
(b) C2 H5OH
CH2 O
CH2 O
(d) CH3CHO
(c) Formaldehyde
(d) Acetaldehyde
CH2 CH 2
D
|
|
+ Zn
product, The product is
Br Br
(a) Ethane
(b) Ethene
(c) Ethyne
(d) 1- bromopentane
(a) 2 CH3CHO
(b) 2 CH3COCH3
(c) 2CH3COOH
(49) A hydrocarbon reacts with hypochlorous acid to give 1-chloro-2-hydroxy ethane, The hydrocarbon
will be
(a) Methane
(b) Ethylene
(c) Ethane
(d) Ethyne
Y
Z
I 2 Excess
(a) C2 HS I
(c) CHI3
(d) CH3CHO
(51) What Would be the product when ethene is Oxidised with Baeyer`s reagent ?
HCH
||
(a) CH2 OH - CH2 OH (b)
O
H C OH
||
(c)
O
132
(d)CO2 + H2 O
(52)
H3C CH CH = CH 2
|
+ HBr A. predominantly product A is
CH3
(a)
CH3CH CH CH 3
| |
Br CH3
(b)
CH3 CH CH CH 3
| |
CH3 Br
Br
CH3 CH CH 2 CH 2 Br
|
(c)
CH3
(b) 2-Chloropropane
(c) 3-Chloropropane
(56)
(b) CH C - CH 2 - CH 2 - CH 3
(c)CH3 - CH = CH - CH = CH2
2 H6
H 2 O 2 /OH R - CH = CH2 B
X
Y. Final product Y is
R CH CH2
| |
(c)
OH OH
CH3 CH CH 2
|
|
(b)
NO Cl
NO
|
(c) CH3 CH 2 CH
|
Cl
(d) |
CH2 CH 2 CH 2
|
NO
Cl
(58) Which of the following sequence of reagents can be used for the Conversion of C6 H5 - CH2 - CH3
into C6 H5 - CH = CH2
(a) SO2 CI 2 ; H2 O
133
(b) 2-methyl-but-2-ene
(c) But-2-ene
(b) Cyclohexane
(c) Cyclohexene
(d)2,3-dimethyl butane
(61) Which of the following represents the given mode of hybridization SP 2 - SP 2 - SP - SP from
left to right
CH
(a)
CH2
CH
(b)
(c)
CH2
(d)
(63) The product obtained when Chloroform is heated with Silver powder is
(a) Ethane
(b) Ethene
(c) Ethyne
(d) Chloromethane
(64) What is the Chief product of reaction between Ethylidene dichloride and alc. KOH / NaNH 2
(a) CH3 - CH2 - CI
(b) CH = CH
. NH
CH3 CH CH 2 + 2 NaNH 2 Liq
X
| |
(65)
Br Br
3
(b)CH3 - CH = CH2
(c) CH3 - C = CH
(b) Ethylene
(c) Acetylene
(b) But-2-ene
(c) Ethyne
(d) But-2-yne
Na / Liq.NH 3
CH 3 CH 2 Br
P
Q
(68) CH CH
196k
(a) CH3 - CH2 - C CH
134
(70) The gas which gives Benzene on passing through a red hot iron tube is
(a) C2 H6
(b) C2 H4
(c) C6 H12
(d) C2 H2
(b) Cyclohexane
(b) Hg +2 / H2 So 4
(d) CH C - Br
b g gives
(b) propanenitrile
(c) Acrylonitrile
(75) What is the product formed when acetylene reacts with hypochlorous acid ?
(a) CH3COCl
(c) Cl 2 CHCHO
(b) Ethane
(c) But-1-ene
(d) Ethene
(79) The Compound X C5 H8 reacts with Ammonical AgNO 3 to gives a white ppt and on oxidation
b g
with hot alk, KMnO4 gives acid CH3 2 CHCOOH there fore X is
(a) Pent-1, 3-diene
(80)
(b) pent-1-yne
CH 2Cl2
Zn / H 2 O
X
Y . End product y is
HC CH + O3
196k
(a)
HCCH
|| ||
O O
CH3 C C CH3
|| ||
(c)
O O
135
(b) 2 CH3COOH
(d) Butanal
CH3CH2 C = CH 2
OH
Na NH 2
X Indentify product X
(83) CH3 - C C - CH3
Paraffin Oil
(a)
CH3 C = C CH 3
|
|
Na NH2
(c)CH3CH2 C CH
(a) Ethene
H 3 PO4
Br2
alc.KOH
B
C
D.
D
(b) Ethyne
(c) Ethane
Lindlars
Catalyst
Na in
Liq.NH3
(b) Ethene
(c) Ethanol
(d) Ethanaime
(b) Li / NH 3
(c) Pd / BaSO4
(d) LiAlH 4
(b) Be2 C
(c) Mg 2 C3
(d) Al 4 C3
(c) 3
(d) 4
(b) 2
(b) Br2
136
(d) Ag ( NH 3 ) 2
(91) Point out the wrong statement in relation to the structure of Benzene.
(a) It forms only one monosubstitated derivative
(b) The C-C bond lenght is benzene is uniformly1.397 A0
(c) It is a resonance hybrid of a number of canonical forms
(d) It has three delocalised p- molcular orbitals
(92) Which of the following when treated with super heated steam under pressure gives benzene?
(a) Benzene Sulphonic acid
(a)
(b)
(c)
(d)
(c)
(d)
(c) phenol
(d) Napthalene
(a)
(b)
..
N
|
H
(b) Toluene
(b) C6 H5COCl
(c) C6 H5COCH3
(d)C6 H5CH3
(a) NO2
(c) NO2 +
(d) NO3 -
+ 3H2
(b) Br -
(c) Br2
(d) Br
(c) Elimination
(d) Rearrangement
[ Ni ]
150 C
(b) Addition
137
(b) Chlorobenzene
(b) -OH
(c) -CHO
(d) -OCH3
(c)-COCH3
(d) -OCH3
conc. HNO3
[ H 2 SO4 ]
(106)
(b) - NO2
X. Product X is
CH3
CH3
NO2
(a)
CH3
(b)
(d)
NO2
NO2
NO2
Cl 2
[Fecl3 ] X. product X is
(107)
NO2
NO2
NO2
(a)
Cl
(b)
NO2
(c)
Cl
(d)
Cl
(a) Phenol
Cl
Cl
(c) Xylene
(d) Benzene
(a)
CH3
CH3
CH3
(b)
(c)
Cl
Cl
COOH
CH2OH
(a)
Cl
(b)
(c)
CH2 Cl
(d)
OH
(d)
(112)
(b)
(113)
(c)
Cl
(d)
Cl
+ 3 HNO3 H2SO 4
(fuming) 111 c X Identify product X
(a) ONT
CH3
Cl
COOH
CHO
(b) PNT
(c) TNT
(d) DNT
110C
Fu min g HNO3
KMnO4 / HF
Soda lim e
P
Q
R
Fu min g H 2 SO4
(b) PTS
(c) TNT
138
(d) TNB
(114) When a mixture of O-bromotoluene and methyl bromide is treated with sodium in presence of
ether it gives
(a)
CH3
(b)
CH3
CH3
CH3
CH3
(c)
CH3
Br
(d)
CH3
CH3
(c) Xylene
(d) Ethylbenzene
(b) Toluene
AlCl3
2 3
2 3
Y
+ CH2 = CH2
X
600 c
(d) Styrene
Br + 2 Na+ Br
+ 2 NaBr
Bi - Phenyl
(a) Wurtz
(b) Fitting
(c) Wurtz-Fitting
(d) Grignard
(119) Benzene on ozonolysis followed by reaction with zinc and water gives
(a) Benzoic acid
(b) Benzaldehyde
(c) Glyoxal
(d) Acetylene
3
2
X
Y In this reaction Y is
(120) C6 H6
H 2SO 4
FeCl3
HNO
Cl
(c) Ethylbezoate
(d) chlorobezene
(b) I > II > IV > III (c) II > I > IV > III (d) IV > I > III > II
(b) Toluene
(c) Hept-2-ene
(d) Hept-1-ene
(b)
(c)
(d)
-
139
(126) In presence of light and heat toluene chlorinated and react with aq. NaOH to give
(a) O - Cresol
(b) P - Cresol
(127) Sulphonation of compound A followed by fusion with NaOH gives mixture of O- cresol & pcresol. compound A is
(a) Benzene
(c) phenol
CH3
(b) Toluene
(d) Benzene sulphonic acid
CH3
CH COCl
[ Anhy. Alcl3 ]
(128)
P
AlCl3
tube
CH Cl
(a) Benzene
(b) Toluene
(c) Chorobenzene
(d) Xylene
A Sn
B
3 PO2
C H
E
D
KOH
0 -5 C
NO2
COOH
(a)
(b)
CH3
COOH
COOH
Br
Br
(c)
Br
(d)
NO2
NO2
(B)
(C)
(D)
(E)
140
A
B
C
D
141
(141) Match the reactions in column I with approp type of reaction as given in column II
column I
CH3
(A)
CH3
CH3
Cl2
[Fe Cl3]
column II
Cl
+
Cl
( i) Alc K O H
( ii) H 2/ N i
CH3
(B) C H 3 C H 2 C l
(C)
C H3 -
( i) H SO / H gSO
( ii) [ AlC l ]3
4
H C = C H 2 4
CCHH
O3
CH = CH2
(D)
(s) Rearrangement
(142)
column I
column II
(A)-CHO
(B)-OH
(C)-NH 2
(R) m-Director
(D)-CI
(143)
column I
column II
(A) Benzene
(B) Ethene
(C) Ethyne
(D) Butane
(a)
CHO
(b)
CHO
H
C=O
C=O
H
CHO
(c)
CHO
(d)
(a)
CHO
(b)
(c)
CHO
142
COOH
(d)
Answer key
1C
2D
3A
4D
5C
6B
7C
8B
9C
10 C
11 A
12 B
13 B
14 B
15 C
16 B
17 A
18 B
19 A
20 B
21 C
22 A
23 B
24 B
25 B
26 C
27 C
28 B
29 B
30 D
31 B
32 A
33 D
34 B
35 B
36 C
37 A
38 D
39 B
40 B
41 D
42 B
43 C
44 C
45 C
46 B
47 C
48 A
49 B
50 C
51 A
52 D
53 C
54 B
55 C
56 B
57 A
58 B
59 B
60 C
61 A
62 D
63 C
64 B
65 C
66 C
67 C
68 A
69 B
70 D
71 C
72 B
73 C
74 C
75 C
76 C
77 B
78 B
79 C
80 A
81 C
82 D
83 C
84 B
85 A
86 A
87 B
88 C
89 A
90 D
91 C
92 A
93 C
94 B
95 C
96 D
97 C
98 A
99 C
100 A
101B
102 D
103 B
104 C
105 D
106 C
107 A
108 B
109 D
110 B
111 A
112 C
113 D
114 A
115 B
116 D
117 D
118 B
119 C
120 B
121 C
122 A
123 B
124 A
143
125 C
126 D
127 B
128 D
129 B
130 B
131 A
132 B
133 C
134 A
135 D
136 E
137 B
138 A
139 B
140 C
141 A. (p), B. (r ), C. (q), D. (p)
142 A. (r ), B. (p), C. (p, q), D. (p)
143 A. (s), B. (r ), C. (q), D. (p)
144 B
145 A
Hints
(1)
(2)
Alkyne Cn H2n - 2 C4 H6
(3)
(4)
cao
soda - lime
Electrolysis
2 CH3CH2 COONa + + 2 H2 O
CH3CH2 CH2 CH3 + 2 CO2 + H2 + 2 Naot
(5)
(6)
1
Boiling a Molecular mass a number of branches
(7)
According to Que-6
(8)
2O
CH3COCl + CH3 MgCl H
CH3COCH3 + MgCl 2
(9)
(10) R - X + 2 Na + R - X Ether
R - R + R - R + R - R
(11) C2 H5 O H + CH 3 Mg Br CH4 + Mg
Br
Oc2 H5
(14) Que-6
1
CH3
CH2 - CH3
3, 3 dimethyl pentane
CH3
(16) The relative stability of conformation isomers of Alkane like Ethane, propane staggered
(Anti) > Skew or Gauche > partial eclipsed > Full eclipsed
(17) The relative stability of conformation isomer of cyclohexane is
Chair > twist boat >boat >half Chair
(18)
(19) 2R - X + Zn R - R + ZnX 2
(Frankland`s Reaction)
Pd /c
(20) C2 H 5Cl + H 2
C2 H 6 + HCl
144
CH3 - CH 2 - CH 2 CH - CH 3
CH 3
isopropyl group
*
hv
CH 3 - CH - CH 2 - CH 3 + Cl 2
CH 2 - CH - CH 2CH 3 + CH 3 - CH - CH - CH 3
(25)
CH 3 Cl
CH 3
Cl
CH 3
(R + S)
(R + S)
Star (*) indicate chiral (assymetric) carbon. Here in both product R and S configurations
are possible so that total 4 chiral compound are possible.
(26) C3 H8 + 502 3CO2 + 4 H2 O
Zn - Cu
CH3 CH CH3 HCl
CH3 - CH - CH 3
C
CH 3CH 2CH 3 + HCl
2 H 5 OH
(27)
2[ H ]
OH
Cl
(28)
iso-propyl bromide
CH3
+ Br2
(30)
+ HBr
1- bromo-1-methyl cyclopentane
4 Br - CH2 - CH2 - Br
b
.KoH
(33) C H C H CI Alc
( b - Elimination reaction)
b
Conc.H SO
2 4
CH - CH3
160 c
OH
145
CH 3
C CH 2CH3
OH
R - CH CH - R
dil aq. KMnO 4
(41) R - CH = CH - R
Room temp.
OH OH
Conc. KMnO 4
(42) R - CH = CH - R
Heat
(Markownikoff)
glycol
R COOH + R - COOH
(43) Ozonolysis
CH2 = CH2 + O3
(44)
CH2
Alk . KmnO4
CH2
Zn
2HCHO
HO
2
OH
OH
Acidic
(45) CH 2 = CH2 + 2 [ 0]
KMnO4 HCHO + HCHO
(46)
CH 2 - CH 2 + Zn
.KOH
(50) CH2 = CH2 HBr
CH3 CH2 Br aq
CH3 CH2OH
CHI3 Iodoform
H+
=
CH - CH 3
(52) CH3 - CH - CH CH2 CH3 - CH -(2
CH3
CH3 )
1, 2
Hydride shift
Br
CH3 CH - CH2 CH 3 Br CH
C
CH2 CH3
3
CH3 (3)
CH3
This reaction follows markownikoff`s rule. Because peroxide effect or Anti markownikoff`s
rule is applicable only to HBr. It is not for HCl and HI.
(55) Ozonolysis of alkene gives two carbonyl group (C=0) for cleavage of each > C = C < s
(i ) O3
CH3CHO + CHO + HCHO
CH3 - CH = CH - CH = CH2
(ii ) Zn / H 2O
CHO
(56) 3R - CH = CH 2 +
1
B2 H 6
2
H 2O2
( R - CH 2 - CH2 ) 3 B
OH -
N-2, OH
HCl
3 R - CH2 - CH
2
+
(57) CH3 - CH = CH2 + N OCI CH3 - CH - CH2
Cl NO
2 CI 2
CH2 CH3 SO
(59) CH3
.koh
CH2 CH2 CI Alc
CH3
KOH
C CH2 - Br alc
.
CH3
CH3
CH = CH 2 + KCl + H 2O
CH3 +
Methyl
C CH2
Shifting
CH3
CH3
CH3
E limination of
C CH2 - CH3
b - Hydrogen
C = CH - CH3
CH 3
3 carbonium (morestable)
CH2
CH
(60) |
CH
CH2
200 c
||
CH2
(Diels-Alder Reaction)
CH2
(61)
SP 2
SP 2
SP
SP
CH2 = CH - C CH
(Colour less)
HC CH + 2 KCl + 2 H2O
Liq . NH 3
CH3 C CH + 2 NaBr + 2 H2O
CH3 CH Cl 2 Br + 2 NaNH 2
Br
147
(66)
D
CH2 - CH2 + 2 KOH ( alc )
HC CH + 2 KBr + 2 H2 O
Br
Br
(Vicinal)
(67) H C COOK
||
OR||
H C COOK
Potasium Maleate
(cis)
(68) HC CH
Acetylene
H C COOK
+ 2H O
2
CH
|||
+ 2CO 2 +2NaOH + H2
KOOC C H
CH
Potasium Fumrate
(trans)
At anode
Na / liq.NH 3
3CH2 Br
HC C Na + CH
Benzene
Nil ( N )2
(71) 4CH CH
( HC = CH ) 4 OR
Cyclooctutetruene
H 2 SO4 / Hg
(72) CH C CH 2 CH 3 + H 2 O
CH2 = O CH2 - CH3
OH
+2
Tax tomerise CH C CH - CH
2
3
3
O
(73) CH CH HBr
CH2 = CH - Br HBr
CH3 - CHBr2
Ethylidene bromide
(74) CH CH HCN
CH2 = CH - CN
HOCI
HOCI
(75) CH CH CI - CH = CH - OH
H2 O
Cl - CH - CH - OH -
CHCI 2
Cl
At Cathode
OH
(76) CH3 - CH 2 - C CH
CH = O
KMnO4 / KOH
(terminal alkyne)
Oxidation of terminal alkyne gives acid and CO 2
KMnO4
(77) CH3 - C C - CH3
KOH CH3COOH + CH3COOH
(nonterminal alkyne)
Oxidation of nonterminal alkyne gives mixture of two acids
(78) CH CH + CH3CH2 MgBr CH3CH3 + CH CMgBr
(79) According to Que-76
148
(80) HC CH + O3 CH
CH
HCCH
|| ||
O O
Zn/ H 2 O
Glyoxal
(81) CH3 - C C - CH3 + O3 CH 3 CH
C C CH
/ H2 O
Zn
CH3 C C CH3
|| ||
O O
CH 3 - C C - CH 3
(85) Alkyne with Lindlar`s Catalysist ( Pd / BaSO4 ) gives Cis- alkene while with Na / Liq. NH 3
(Birch Redaction) gives trans-alkene
pd
(86) CH CH + 2 H2 Ni/
CH3 - CH3
Mg 2 C3 + 4 H2 O CH3 - C CH + 2 Mg ( OH ) 2
1- Alkyne will give reaction while 2- Alkyne will not give reaction
SO3 H
D
+ H2 O (g )
(92)
+ H2 SO4
(93) 6 p electrons
(94) According to Hukels Rule Compound to be aromatic it should have ( 4 n + 2 ) p e s i.e It
should have 2,6,10,14 p e electrons. But cyclo octa tetraene has 8 p e so it is non-aromatics
OH
(95) phenol
(96)
(97)
CH 3COCl
[ Al Cl ]
3
Acetophenon.
(98) Nitration, Sulphonation, Halogenation, Alkylation and Acylation of Benzene are Electro
philic Substitation Reactions.
+
(100) Br + is electrophile
(101) Beacause double bonds of Benzene breaks on addition of H2
Cl
Cl
Cl
hv
+3Cl 2
Cl
(102)
Benzenehexachloride(BHC)
Cl
Cl
Cl
(103)
+ HCI
+ CI 2
[ FeCI3 ]
conc.HNO3
[ H SO ]
(106)
CH3
CH3
CH3
CH3
CH3
Cl2
[ FeCl ]
(107)
Cl
CH3
CH3
OH
(108)
Zn
O-Cresol
+ Zno
Toluene
CH2 Cl
CH3
Cl2
uv
(109)
Benzylchloride
COOH
CH3
KMnO4 / H
3[O ]
+
(110)
CHO
CH3
CrO2 Cl2
2[O ]
(111)
+ H2 O
+ H2 O
CH3
CH3
O2N
NO2
H 2 SO 4
+3 HNO3
111 c
(112)
2,4,6-Trinitrotoluene(TNT)
NO2
CH3
CH3
O2N
(113)
COOH
NO2
KMnO 4
H+
NO2
NO2
NO2
NO2
NO2
Soda lim e
NO2
NO2
1,3,5-Trinitrbenzene(TNB)
CH3
(114)
CH3
Br
+ CH3 Br + 2 Na
ether
CH3
+ 2 NaBr
O-Xylene
This is known as wurtz- Fitting Reaction
150
COOH
COOH
COOH
Phthalic acid
Isophthalic acid
Terthalic acid
CH2 = CH 3
CH = CH2
(116)
COOH
H2
Ni+
Styrene
Ethylbenzene
CH2 = CH 3
(117)
CH = CH2
[O ]
600 C
AlCl 3 ]
+ CH2 = CH2 [
,
+ H2
CH3
CH3
CH2
[ Al O + Cr O ]
CH2
|
(123)
CH2
2 3
2 3
CH3
+ 4H2
[o ]
|
Toluene
CH2
CH2
n-Heptane
OH
(124)
Zn
+ Zno
(125) p e s in , , , are 4,4,6,4 there for according to Hukelis Rule (c) is Aromatic
CH3
CCl3
3 Cl / hv
Heat
(126)
COOH
3 NaOH
CH3
(127)
Sulphonation
Compound A
(Toluene)
CH3
CH3
CH3
+ 3NaCl + H 2O
SO3H
NaOH
fusion
+
So3H
151
CH3
OH
+
OH
H2 O
(129) CaC2 2
HC = CH + Ca ( OH ) 2
CH3
CH Cl
hot iron
3CH = CH
tube
CH3
Br
Br2
Br
/ HCI
Sn
NO2
NO2
NaNO / HCl
0.5 c
NO2
CH3
COOH
CH3
H PO
Br
+ HCI
CH3
CH3
(130)
[ AlCl ]
3
2
2[ H ]
Br
Br
KMnO
KOH
[O ]
N = N Cl
(131)
N
|
H
6 p e s ( 2 2 p -bonds + lonepair of N)
(132) Correct explanation :- Chlorination of CH 4 is free radical reaction and free radicals are
obtained in sunlight.
CH3
|
(133) CH3 C CH3
|
CH3
3
(144)
Zn / H O
2
CHO
CHO
aq. KOH
CHO
152
2.
SP 3
SP
(C)
SP 2
(D)
(C)
chloramphenicol (D)
B&C
chloroquine
3.
4.
(B)
(B)
chloroform
chlorapetite
(i)
Goiter
(p)
Anaesthetic
(ii)
Malaria
(q)
(iii)
Typhoid fever
(r)
chloroquine
(iv)
haloethane
(s)
chlor amphenical
(v)
(t)
Thyroxine
(A)
(B)
(C)
(D)
(A)
5.
(B)
(C)
CI
(i)
CH3
CH2 Cl
(ii)
(p)
2, chloro toluene
(q)
1, Benzyl chloride
(r)
1, chloro toluene
(s)
chlorophenyl methane
(t)
(A)
i - t, ii - s
(B)
i - p, ii - s
(C)
i - r, ii - q
(D)
i - r, ii - q
153
(D) A & C
6.
7.
(B)
10
(C)
CH3
CH3
H
H Br
H
H
(B)
H
H 3C
CH3
H
CH3 BR
(D)
(D)
H
H
H BR
CH3
H
H Br
(A)
OH
(C)
(D)
N+
2 X
OH
+ HCl + N
N+2 X
273278K
+ H 2O
(B)
N=N
(D)
+ KI
+ N2
OH + HCl
?
X ; X = .............
+ HBr
(A)
Above all
H
9.
(C)
8.
Br
H
HH
(B)
(C)
Br
HH
HH
H
H
None of these
H
CH 2C = CH 2
10.
+ HBr Peroxide
Y. For Y =
CHCH
CH 3
2
(A)
CH 2 CH 2CH 2 Br
(B)
Br
CH 2 C CH 3
(C)
CH CH 2 CH 3
(D)
Br
154
Br
11.
(CH )
CO
(i)
2
CH 3 Br + NaI 3
CH 3 I + NaBr
(ii)
2CH 3 Br+Hg 2 F2
2CH 3F+Hg 2 Br2
x : Finkel stein
12.
14.
15.
16.
3 2
CH 3CH 2Cl+NaI
C2 H5 I+NaCl
(iv)
2C 2 H 5 Br + COF2
2C 2 H 5 F + COBr2
(v)
COF2 + 2CH 3 Br
2CH 3 F + COBr2
(A)
(B)
(C)
(D)
y : Swart reaction
R - OH + PX 3
R - X + Z. For Z = ..................?
(A)
13.
( CH )
(iii)
X 2 PO 4
(B)
x + HCl
Aniline
=Y
HPO3 X 2
N+
2X
(C)
H 2 PO3 X
(D)
H 3 PO 3
(A)
NH 3 , 298 - 300K
(B)
(C)
(D)
NaNO, 298 K
(B)
(C)
(D)
For nucleophilic substitution bimolecure SN2 reaction give the correct order of reactivity.
(A)
(B)
(C)
(D)
In the following pairs of halogen compounds which would undergo SN2 reaction faster ?
(A)
(C)
CH 2Cl
(B)
Cl
Cl
(D)
155
Cl
None of these
17.
18.
19.
(B)
(D)
Br
CI
a&b
(B)
Br
(C)
Br
20.
CH 3CH 2 CH 2 CH CH
OH
3
OH
Br
21.
22.
CH 3 CH 2 CH 2 CH = CH
x - pent 1 - ene
CH 3 CH 2 CH = CH CH
y - pent 2 - ene
(B)
(C)
C 6 H 5CH 2 Br < C 6 H 5CH (CH 3 )Br < C 6 H 5CH (C 6 H 5 )Br < C 6 H 5C(CH 3 )(C 6 H 5 )Br
(D) b & C
Predict the true R or S for the following structres
r
(i) s
q
r
(ii) s
(iii) q
r
p
P = I; Q = Br, S = Cl; r = H
(A) i - S ii - R, iii - R
(C) i - S ii - R, iii - S
(B)
(D)
156
i - R ii - R, iii - S
i - S ii - S, iii - R
( C6 H 5 ) Br
23.
24.
25.
26.
27.
29.
30.
31.
(B)
(C)
(D)
(B)
(C)
(D)
(A)
CH 2 OCl
(B)
CH 2 Cl 2
(C)
COCl
(D)
COCl 2
Alkoh olic
A
KOH
CH 3CH 2 CH2 I
NaNH 2
C For ; C
- NH 3
- NaBr
Br 2
B
Alkoholic KOH
(A)
Alkenol
(B)
Alkene
(C)
Alkaiene
(D)
Alkele amine
For given compounds gives proper reactivity order for SN1 reaction.
(x)
28.
Me
Me
(y)
Br
Me
Br
(z)
Br
Me
(A)
Z>X>Y
(B)
X >Y> Z
(C)
Y>Z>X
(D)
X>Z>Y
(C 2 H 5 )2
(C)
CH 3Cl
CHCl
(B)
(CH 3 )3 CCl
(D)
(CH 3 )3
C.Cl
CH 3CH 2Cl + Ag CN
(A)
CH 3CH 2 CN
(B)
CH 3CH 2 N = C
(C)
CH 3CH 2 N = C
(D)
a&b
Propine
(B)
I-chloro ethene
(C)
ethene
(D)
1-chloro propane
2, chloropanten
(B)
1-chloropanten
(C)
(D)
157
32.
Cl
Cl
33.
Cl
34.
Cl
H 2N
37.
i - R, ii - S, iii- R, iv - R
i - R, ii - S, iii- S, iv - S
Br
(A) R and R
(B)
(C) S and S
(D)
2
Predict the order of reactivity in R-X for SN reaction.
(A) R-F >>R-Cl > R-Br > R-I
(B)
(C) R-F < R-Br < R-F < R-Cl
(D)
Freons which is use in industry
R and S
S and R
R-I > R-F > R-Cl > R-Br
R-F << R-Cl < R-Br < R-I
(A)
6 -( CCl2 F2 )
(B)
4 - CCl2 F3
(C)
10,- CCl 2 F2
(D)
12,- CCl 2 F2
38.
39.
(B)
(D)
CH 2OH
36.
CH 3
COOH
35.
(B)
(D)
(i)
(ii)
(iii)
(iv)
(v)
D.D.T
Iodo form
Carbon tetra chloride
Freon
CHCl3
(a)
(b)
(c)
(d)
(e)
Dry cleaning
Freon refrigerant R-22
For air conditioning
antiseptic
an insecticide
(A)
(C)
(B)
(D)
158
40.
CH
(1)
41.
42.
Pho -
CH 3O -
(3)
OH -
(4)
AcO-
4>3>2>1
(D)
(A)
I - < Cl - < Br -
(B)
Cl - < Bi - < I -
(C)
I - < Br - < Cl -
(D)
Br - > Cl - > F -
(A)
(B)
CH 3
(C)
H
CH 3
COOH
COOH
H 2N
NH 2
COOH
CH 3
NH 2
COOH
43.
CH 3
(D)
1.
p. elimination reaction
2.
q. substitution reaction
3.
KOH + Ethanol
CH 3CH 2
Ethene
D
|
Cl
r. courtz reaction
+ + OH
4.
(A)
(C)
(B)
(D)
s. grignard reaction
1-s, 2-r, 3-q, 4-p
1-s, 2-r, 3-p, 4-q
44.
A
(1)
(2)
Cl
2
Br
B
+ 2NaCl
+ 2Na Ether
CH3
+ 2NaCl
+ 2Na + CH 3 Br Ether
Cl
(3)
+ 2NaCl
O
O
(A)
(B)
(C)
(D)
45.
Na / Ether
R' X
. Identify R1
CH 3
(A)
(C)
46.
CH 3 - C - CH 3
|
CH 3
|
(B) CH 3 - C |
CH 3
CH 3
|
CH 3 - C - CH 2|
CH 3
CH 3
|
(D) CH 3 - C |
CH 3
Mg
H 2O
B.
Mg Br
Mg Br
(A)
(B)
Mg Br
Mg Br Br
(C)
48.
CH 3
|
C |
CH 3
47.
CH 3
|
C - CH 2 |
CH 3
(D)
For recemisation.
(A) 50 : 50 mixture & opticall active.
(B) 75 : 25 mixture & optically inactive
(C) 50 : 50 mixture & optically inactive
(D) 25 : 75 mixture & optically active
Classify the configuration of product of a symmetric carbon atom. Consider the replacement of a
group X by Y in the following reaction.
C 2H 5
H 3C
C 2H 5
x
H
CH 3
C 2H 5
CH 3
A+B
160
49.
Predict the conect order for following reaction the approaching nucleophilies.
P = Nu :
CX
q Nu :
H H
50.
51.
54.
55.
Nu :
H CX
; S
(A)
NaNO2 + 2 HCl
C6 H 5 NH 2
C6 H 5 N 2Cl + NaCl + H 2O
273 - 278 K
(B)
C6 H 5 N 2Cl
C6 H 5 Cl + N 2
DCuCl2 + HCl
(C)
C6 H 5 N 2Cl
Send Mayur
C6 H 5 Br + N 2 + HCl
DCuCl2 + HBr
Nu :
CX
KI
D
C 6 H 5 N 2 Cl
C 6 H 5 I + KCl + N 2
(A)
53.
(D)
52.
H
H C X ;
H
PCl 3
(B)
SOCl 3
(C)
PCl 5
(D)
SOCl 2
161
56.
1.
2.
3.
4.
Benzail Bromaid
Ethilidin bromaid
Finail Bromaid
Alail Bromaid
M.
N.
O.
P.
CH3CH2Br2
H2C = CHCH2Br
(A)
(C)
(B)
(D)
Br
CH 2Br
Cl
57.
58.
Cl
(A)
Cl
(B)
H
H
59.
60.
61.
(C)
H
(D)
Cl
Cl
H 3 PO 3
(B)
HPOX 3
(C)
POX 3
(D)
H 3 PO 4
C 2 H 5 I AgNO
2 X. ..............?
(A)
C2H5 - O - N = O
(B)
C2H5 - N = O
(C)
C 2H 5 O N
O
Ag
(D)
C 2H 5 O N
O
O
162
62.
63.
64.
65.
66.
(A)
(B)
(C)
(D)
X
Y
Benzene
Chlorobezene
For X & Y respectively..
(A)
Cl 2 , [FeCl3 ] ; Cl 2 [FeCl3 ]
(B)
(C)
(D)
Silver nitrate not giving the Precipates with chloro form because of .............
(A)
(B)
(C)
(D)
Chlorobenzene
(B)
ChloroTolune
(C)
Benzyl Chloride
(D)
Chloro phenol.
(C)
a&b
67.
68.
DDT
(B)
BHC
(D)
None of these
Formile Chloride
(B)
Formic Acid
(C)
Cl 3C - COOH
(D)
COCl 2
(B)
CH 3CHO
(D)
Benzophenone
C 2 H 5OH
COCH 3
(C)
69.
70.
71.
(B)
(C)
(D)
What is DDT ?
(A)
Insecti side
(B)
Bleaching agent
(C)
Weedkiller
(D)
Oxydiging agent
Bl2 / FeBr3
(B)
HBr
(C)
Bl2 / Light
(D)
Br2
163
72.
73.
74.
75.
CH 3 - F,
(B)
CH 3Cl
(C)
CH 3 I
(D)
CH 3 . Br
CH 2CH 2Br
CH 2CH 3
(A)
Br
(B)
CH 2CH 3
CH 2CH 3
(C)
(D)
Br
76.
77.
78.
79.
80.
Br
3 .......... ?
(A) propile benzene
(B)
(C) 3-propile 1-chloro benzne
(D)
For Lucast test............
n-propile benzene
none of these
(A)
(B)
(C)
(D)
HCl + ZnCl 2( aq )
(B)
(D)
1,1 dichlorobutane
none of these
164
81.
82.
(1)
83.
(2)
(3)
CH 3
C
CH 3
(1)
+ CH 2
+ CH 2
(2)
(3)
84.
Cl
(B)
Cl
Cl
CH3
(C)
(D)
85.
86.
87.
(ii)
(iii)
Br
Br
(A) IV > III > I > II
(C) I > IV > III > II
The reactivity of the compounds............
(I) MeBr
(III) MeCl
(A) I > II > III > IV
(C) IV > III > I > II
Cl
CH3
(iv)
(B)
(D)
Br
I > II > IV > III
I > IV > II > III
(II)
(IV)
(B)
(D)
PhCH2Br
P - Meo C6H4Br decreases as
IV > II > I > III
II > I > III > IV
Br
165
Br2 / Fe
CH2CH = CH2
88.
Br2 / Water
(A)
Br
Br
(C)
; x & y respectively
CH2CH = CH2,
CH2 CH2Br,
(B)
Br
CH2 CH CH2 Br
|
Br
CH2 CH CH2
|
|
Br Br
CH2 CH = CH2,
CH2 CH2 Br
Br
89.
90.
91.
92.
93.
(B)
(D)
The no. of structural & configurational isomers of a bromo compound C5 H 9 Br obtained by the
addition of HBr on 2-pentyne respectively are............
(A) 2, 4
(B) 4, 2
(C) 1, 2
(D) 2, 1
HBr
Hint : CH3 - CH2 C - CH3
CH3 CH2 - C = C - CH3 ; CH3 CH2 - C = C- CH
3
|
|
|
|
H Br
Br H
Thus, each one of the these will existas (I) as a pair of geometrical isomer. Structural isomers = 2 &
stereosomers = 4.
How many enantiomer pairs are obtained by monochlorination of 2, 3-dimethyl butane ?
(A) two
(B) three
(C) four
(D) one
Which intermidiat increase the SN2 reaction ?
(A) carboniyan ion
(B) activated complex ion
(C) Freeredical
(D) carbenion ion
3CCl 4 + 2SbF3
SbCls
high Pr essure
A + 2SbCl 3 ; A = .....................
(A)
CH 2 Cl 2
(B)
CCl 3 F
(C)
CCl 2 F2
(D)
CClF3
166
94.
95.
96.
97.
98.
99.
CCl 4
(B)
CHI 3
(C)
CHCl 3
(D)
CCl 2 F2
CH3
|
H C D Which is the configuration of this compound.
|
Br
(A) S(B) R (C) L (D) D Reaction of chlorobenzene with Mg in presence of dry other will gives compound A. Compound A
reacts with aqueous halogen acid give which product.
(A) Phenol
(B) Phenyl Ether
(C) Phenyl ketone
(D) Benzene
In sulfonation of chlorobenzene gives ................
(A) Benzen sulfonic acid
(B) m-chloro benzene sulfonic acid
(C) O & P Chlorobenzen sulfonic acid
(D) O-chlorobenzen sulfonic acid
C2H5I
Ethenol
KOH
Br2
A
B ; Where B = ................
(A)
CH 3 - CHBr2
(B)
CH2Br CH2Br
(C)
CH.Br = CH.Br
(D)
CH 3CH 2 Br
CH 3Cl ; CH 3 - Br, CH 3 - F
(B)
CH 3 Br, CH 3 - F, CH 3 - Cl
(C)
CH 3 - CI ; CH 3 - F, CH 3 - Br
(D)
CH 3 - Br, CH 3 - Cl, CH 3 .F
Cu 2 (CN )2 + KCN
(B)
Cu 2 Cl 2 + HCl
(C)
Cu 2 I 2 + KI
(D)
Cu 2 Br2 + HBr
CH3
101. H3C
(A)
(C)
(B)
(D)
167
(B)
(D)
Tras 2-Butene
1-Butene
(A)
DCH2CH2CH2Cl
(B)
CH 3CH.D.CH 2 Cl
(C)
CH 3CH.Cl.CH 2 D
(D)
CH 3CH 2 CH.D.Cl
3-chlorobutene
tertiary butile chloride
(B)
(D)
109. C3 H 8 + Cl 2 light
168
CH 4 + HF
(B)
CH 3OH + HF
(C)
CH4 + F2
(D)
CH 3 Br + AgF
CH 2 = CHCH 2 Cl
(B)
C6H5Cl
(C)
C6H5CH(CH3)Cl
(D)
C 6 H 5CH 2 Cl
(A)
HO
(B)
CO2H
H
(C)
CO2H
OH
CO2H
(D)
CO2H
H
Cl
C 6 H 5CH 2 Br
(B)
C 6 H 5C(CH 3 ) (C 6 H 5 ) Br
(C)
C 6 H 5 CH (C 6 H 5 ) Br
(D)
C 6 H 5CH (CH 3 ) Br
Me
CH2Br
119.
Anhy.AlCL3
(B)
(D)
C;C=?
(A)
CH3
Br
(B)
CH3
(D)
None of these
(C)
CH3
169
120. The number of isomers for the compound with colecular formula C2BrClFI is ...
(A) 3
(B) 4
(C) 6
(D) 5
121. In the presence of peroxide, hydrogen chloride and hydrogen iodide do not give anti Markovnikov
addition to alke nes because.
(A) both are hightly tonic
(B) one is oxidising and other is reducing
(C)
(D)
CH 3CHO
(B)
CCl3CHO
(C)
CHCl 3
(D)
(CH 3 )2 O
(A)
CH3CH.Br.CH2
OH
(B)
CH3CH2CH.Br
(C)
CH3CH2CH.Br
OH
(D)
CH3 CH.Br.CH2
(B)
Hydrohelognation reaction
Br
Br
O-cresol
Ben zoic Acid
(B)
(D)
170
P-cresol
2, 4 dihydroxy toluene
130. 2-Phenyl 2-chloro propane on treat ment with alcok gives mainly.
(A) 2-phenyl propene
(B) 3-phenylpropane
(C) 1-phenyl propan 2-ol
(D) 1-phenyl propane 3-ol
131. Only two isomeric monochloro derivaties are possible for
(A) n-hexane
(B) 2, 4 dimethyl pentane
(C) benzene
(D) 2, methyl propane
132. The C-H bond distance is longest in
(A)
C2H 2
(B)
C2H 4
(C)
C 2 H 2 Br
(D)
C2H6
Answer Key
1. c
2. c
3. d
4. c
5. b
6. d
7. c
8. b
9. c
10. c
11. c
12. d
13. c
14. c
15. b
16. a
17. b
18. c
19. a
20. b
21. b
22. b
23. d
24. b
25. d
26. c
27. b
28. c
29. c
30. b
31. c
32. a
33. b
34. c
35. c
36. d
37. d
38. a
39. b
40. c
41. b
42. c
43. d
44. d
45. a
46. d
47. c
48. a
49. b
50. b
51. b
52. d
53. c
54. d
55. a
56. b
57. b
58. a
59. c
60. d
61. c
62. d
63. d
64. b
65. c
66. b
67. d
68. d
69. b
70. a
71. a
72. a
73. d
74. b
75. d
76. b
77. c
78. a
79. a
80. b
81. d
82. b
83. c
84. c
85. b
171
86. c
87. d
88. a
89. b
90. a
91. d
92. b
93. c
94. b
95. a
96. d
97. c
98. b
99. c
100. c
101. a
102. b
103. a
104. b
105. d
106. c
107. c
108. b
109. c
110. b
111. b
112. d
113. d
114. b
115. b
116. b
117. b
118. c
119. b
120. c
121. c
122. b
123. c
124. c
125. c
126. d
127. c
128. c
129. c
130. a
131. d
132. d
133. a
134. b
2.
3.
4.
5.
Preparation of alcohols:
Monohydric alcohols are prepared by the hydrolysis of alkyl halides with aqueous
alkali, hydration of alkenes, hydrolysis of ester, reduction of (alde hydes, ketones,
acids and acid derivatives). Grignard reagents is also used to prepare monohydric
alcohols.
Physical properties of alcohols:
The boiling points of alcohols are much higher than comperatively same molecular
masses of alkanes, ethers and alkyl halides. This is due to intermo lecular Hbond. For isomeric alcohols, the boiling points are in the order 10 > 20 > 30.
Due to the formation of H-bond between alcohol and H2O modecules,
alcohol with lower number of carbons are soluble in water.
Chemical properties of alcohols:
Alcohols exhibit three types of reactions,
(i) Reaction in which O-H bond cleaves
(ii)Reaction in which C-O bond cleaves
(iii)Reaction in which whole molecule of alcohol participate.
Victor-Meyers test and Lucas reagent are used to distinduish 10 , 20 and 30
alcohols.Oxidation reactions are also used to distiguished between 10, 20 and
30 alcohols.
Preparation of phenol:
Phenol is prepare from cumene, diazonium salt, benzene and coal tar.
Physical properties of phonol:
Phenols have higher boiling point than the corresponding hydrocarbon and
aryl halides. This is due to the presence of intermolecular hydrogen bonding.
Phenols are more acidic than alcohols because phenoxide ion is stabilised by
resonance. The presence of electon withdrawing group like NO2, increases the
acidic strength of phenol and electron donating group like R, decreases the
acidic strength of phenol.
172
6.
7.
8.
Carbonyl compounds:
+
Organic compounds containing carbon-oxygen double bond ( C = O)
O are
C called
C carbonyl
=O
group or carboxy group compounds. In aldehydes, the carbonyl group is attached to one hydrogen
atom and one alkyl (or aryl or hydrogen atom) group, while in ketones it is attached to one alkyl
and one arly group or to two alkyl (or aryl) groups, which may be same or diffrent. If carbonyl
group is attached to one hydroxyl group, the compounds are know as carboxylic acids. In carboxylic
acid compounds, if the hydrogen of hydroxyl group is substituted by alkyl or aryl group the
compounds are known as esters, but if it is substitued by acyl group, the compounds are known as
acid anhydrides. If the carbonyl group is attached to chlorine and to amino group the compounds
are known as acid chlorides and amides respectively. The general formula of these compounds are
expressed as
Aldehyde
Anhydride
2.
Carbonyl carbon atom is sp 2 hybridised and form three s -bonds and one p bond. All the three
s-bond lie in same plane having angle 1200. The p- bond lies both above and below the C-O
s bond. Thus the carbonyl carbon, oxygen atom and two atoms which are directly bonded to the
carbonyl carbon lie in one plane, and is confirmed by electron diffraction and spectroscopic studies.
Due to higher electronegativity of oxygen atom relative to carbon atom the carbonyl group is
polarized and carbonyl carbon becomes electrophile (Lewis acid) and oxygen becomes nucleophile
(Lewis base). Carbonyl group is polar in nature and has dipole moments.Aldehydes and ketones
173
have dipole moments 2.3-2.8 D. The resonance structures are as shown below :
C= O C
+
C =O
3.
The polar carbonyl groups have dipole-dipole interaction between opposite ends of the C = O
O C
group dipoles and hence due to weak intermolecular attraction the melting points and boiling points
of aldehydes and ketones are higher than corresponding non-polar compounds.
The order of boiling points is carboxylic acid > alcohol > isomeric ketone > isomeric aldehyde
> ether > hydrocarbon.
Due to hydrogen bonding with water molecules the aldehydes and ketones upto three carbon are
soluble in water.
The aromatic aldehydes and ketones due to presence of larger hydrocarbon parts (like benzene
ring etc.), are insoluble in water.
All adehydes and ketones are fairly soluble in organic solvents like benzene, ether, alcohols,
chloroform etc.
Chemical properties of aldehydes and ketones:
Due to presence of hydrogen atom, the carbonyl group of aldehyde is much more reactive
than ketone.
Aldehydes and ketones undergo nucleophilic addition reaction because the carbonyl carbon atom
is slightly positively charged.
In nucleophilic addition the first step is reversible and also slow, so it is a rate determining step.
The second step is reversible.
Due to steric effect and inductive effect the aldehydes are more reactive than ketones.
Most of the aldehydes and aliphatic methyl ketones, due to less steric hindrance are more reactive.
4.
Aldehydes and ketones react with NaHSO3 and give bisulphite addition product which are usu
ally crystalline solids. On hydrolysis they give original aldehydes and ketones, so this reaction is
useful for separation and purification of aldehydes and ketones.
Addition of HCN and Grignard reagent to the aldehyde and ketone which give a -hydroxy carboxylic
acid and 10 , 20 ,30 alcohols respectively..
Addition of alcohol to aldehyde give hemiacetal and further acetal, while ketone give the same
product.
Nucleophilic addition reaction of aldehydes and ketones with NH 3 and its derivatives ( H 2 N - Z )
are catalysed by acids.
Aldehydes and ketones on reduction give 10 and 20 alcohols respectively..
Aldehydes and ketones can be reduced to hydrocarbon by using different reagent like WolffKishner reduction, Clemmenses reduction, red phosphorus with HI. Ketones on reduction with
magnesium amalgam and water give the product pinacol. Oxidation of aldehydes : Tollens test,
Fehlings test and Benedicts test give the product carboxylic acid. Fehlings test and Benedicts
test are not given by aromatic aldehydes.
Oxidation of ketones by strong oxidizing agents like con. HNO3, KMnO 4/ H 2SO 4,
K2Cr2O7/H2SO4 give mixture of carboxylic acids.
174
+
C =O
Oxidation of aldehydes and ketones containing CH 3CO -group give iodoform test.
5.
6.
Aldol condensation and cross aldol condensation are the reactions given by aldehydes and ketones
having a -hydrogen atom or atoms using dilute alkali as catalyst.
Cannizzaro reaction is given by aldehydes and ketones which do not have an a -hydrogen atom
by using con. NaOH or 50 % NaOH.
Electrophilic substitution reactions of aromatic aldehydes and ketones are nitration, sulphonation
and halogenation.
Preparation of caroxylic acids :
Carboxylic acids are prepared from :
Primary alcohol and aldehyde
Alkyl benzene and alkenes
Nitriles and amides.
Grignard reagents
Acid halide (chloride) and anhydrides
Esters
Acidic nature of carboxylic acids :
Carboxylic acids are stronger acids than phenol and alcohols.
For convenience the strength of an acid is generally indicated by its pK a value rather than its K a
value.
pKa = log Ka
7.
175
MCQ
1.
2.
3.
4.
5.
(B) 8
(C) 6
(D) 9
Which of the following will produce only one product on reduction with LiAlH4 ?
(A) CH3COOCH2CH3
(B) CH3CH2OCOCH2CH3
(C) CH3COOCH3
(D) CH3CH2OCOCH2CH2CH3
LiAlH 4
H 2 C = CH - COOH
X . What is "X" ?
(B) CH 3CH 2 CH 2 OH
(C) H 2C = CH - CH 2OH
P+I
H O
Mg
HCHO
A
B
C
D,
In the following Sequence of reactions, CH 3CH 2OH
ether
2
6.
(A) propanal
(C) butanal
7.
8.
During dehydration of alcohol to alkenes by heating with Conc H2SO4, the initiation step is:
(A) elimination of water
(D) II and IV
9.
Which of the following alcohal on heating with conc H2SO4 gives product, which show geometrical
isomerism ?
(A) 2,4- dimethyl pentan-3-ol
(C) butan-2-ol
(D) all of the above
10. Propan -l-ol and propan-2-ol can be distingaished by
(A) oxidation with alkaline KMnO4 followed by reation with Fehing Solution
(B) oxidation with acidic dichromate followed by reation with Fehling Solution
(C) oxidation by heating with copper followed by reation with Fehling Solution
(D) oxidation with conc H 2SO 4 followed by reaction with Fehling Solution
11.
Which one of the follwing will most readily be dehydrated in acidic condition ?
O
(A)
OH
(B)
(C)
(D)
OH
OH
12.
The most suitable reagent for the conversion of primary alcohol into aldehyde with the same number of
carban is
(A) acidified K2Cr2O7
(B) alkaline KMnO4
(C) acidified KMnO4
15.
Na
P + Br
OH
x
y What is y ?
2
(A)
16.
(B)
(C)
(D)
An organic compound "X" on treatment with PDC in CH 2Cl2 gives compound "Y". Compound "Y",
reacts with I2 and alkali to form yellow precipitate. The compound "X" is
(A) acetone
(B) ethanal
(C) ethanol
177
17.
How many optically active stereoisomers are possidle for butan -2,3 -diol ?
(A) 1
18.
(B) 2
20.
(D) 4
(I)
(III)
(II)
(IV)
(C) 3
(B) hybridization
An organic compound X is oxidised by using acidified K 2Cr2 O7 . The product obtained reacts with
phenyl hydrazine but does not give silver mirror test. The possible structure of X is
21.
(A) CH 3 CH 2 OH
(B) CH 3 CO CH 3
(C) ( CH 3 )2 CH OH
(D) CH 3 CHO
22.
24.
25.
(D) ( CH 3 )3 CD
23.
(C) aldehydes
______________alcohol reacts immediately with anhydrous ZnCl2 + HCl and gives insoluble chloride
(A) Methanol
(B) Ethanol
26.
(i ) B H
2
6
P
(ii ) H O / OH -
2
(A) Both
ku
27.
H O
CH2 ........
Q P and Q respecctively are
3
CH2OH
(
Bk
)u
CH3
OH
(C)
CH2OH
and
C
CH
H32
H3
(D) CHCOH
2OHand
OH and
CH2OH
(A) Br2 + H 2 O
(B) I2 + NaOH
(C) FeCl3
28.
(B) CH 2 Cl CH 2 OH
(C) CH Cl2 CH 2 OH
30.
When a compound (Molecular formula C3H8O ) is treated with acidic sodium dichromate we get
compound "X". When"X" is treated with methyl magnesium bromide followed by hydrolysis compound
"y" is formed. The compound y is
(A) isopropyl alcohol
(B) tertiary butyl alcohol
(C) iso butyl alcohol
(D) methyl ethyl ketone
31. Idenfify P,Q and R in the following reactions,
(i) OH
(ii)
COOH
OH
OH
Zn
Q
D
C2 H 5 I
(iii) R
OC 2H 5
33.
CHCl3
50%KOH
KOH
OH
CH
(A)
OH
(B)
OH
OH
CH2 OH +
(C)
OMe
34.
OH
Given I =
COOK
, III =
OH
OH
COOK
CH2 OH +
(D)
NO2
, II =
OH
COOK
An organic compound `X' With molecular formula, C7 H8O is insoluble in aqueous NaHCO3 but
dissolves in NaOH . When treated with bromine water, `X' rapidly gives `Y' ( C7 H5OBr3 ) The
compounds `X' and `Y' respectively, are
(A) benzyl alcohol and 2,4,6 - tribromo-3-methoxy benzene
(B) benzyl alcohol and 2,4,6 - tribromo-3-methyl phenol
(C) o-cresol and 3,4,5 -tribromo-2- methyl phenol
(D) m-cresol and 2,4,6 -tribromo -3- methyl phenol
36. Willamson's Synthesis is used for the preparation of
(A) acid
(B) ester
(C) ether
(D) alcohol
37. P - cresol reacts with chloroform in alkaline medium to give the compound A, which adds hydrogen
cyanide to form the compound B. The latter on acidic hydrolysis gives chiral carboxylic acid. The
structure of the carboxylic acid is
CH3
CH 3
(A)
OH
CH2COOH
(B)
OH
CH3
CH3
(C)
CH(OH)COOH
CH2 COOH
(D)
OH
OH
180
CH(OH)COOH
38.
OH
(A)
(B)
(C)
(D)
NO2
NO2
39.
OH
OH
CH 3
The Structure of the compound that gives a tribromo derivative on treatment with bromive water is
CH3
(A)
(B)
OH
CH3
(C)
CH2 OH
CH3
OH
(D)
OH
40.
(I) Benzene 1,2 - diol (II) Benzene 1,3 -diol (III) Benzene 1,4 -diol (IV) Phenol
The incresing order of boiling points of above mentioned compounds is
(A) I < II <III < IV
(B) I < II < IV < III
(C) IV < I < II < III
(D) IV < II <I < III
41. Phenols are more acidic than alcohols because
(A) phenols are more soluble in polar solvents
(B) phenoxide ion is stabilised by resonance
(C) phonoxide ion do not exhibit resonace
(D) alcohols do not lose H atoms at all
42. The products obtained when benzyl phenyl ether is heated with HI in the mole ratio 1:1 are
1. phenol, 2 benzyl alcohol, 3. benzyl iodide, 4. iodobenzenc
(A) 1 and 3 only
(B) 3 and 4 only (C) 1 and 4 only
(D) 2 and 4 only
43. The product obtained by the reaction of HBr with phenol is
(A)
44.
HO
Br
(A)
N=N
(C)
Br
OH
(B)
Br
(C)
Br
OH
Br
+
Base
N2 Cl
OH
(B)
(D)
181
OH
45.
Which one of the following is reduced with zinc and hydrochloric to give the corresponding hydrocarbon?
(A) Ethyl acetate
(B) Acetic acid (C) Acetamide
(D) Butan -2-one
46. An organic compound x with molecular formula C5H10O yields phenyl hydrazone and gives a negative
response to the iodoform test and Tollen's test. It produces n-pentane on reduction. The compound could be.
(A) petanal
(B) pentan-2-one (C) pentan-3-one
(D) amyl alcohol
47. Which of the following on heating with aqueous KOH, produces acetaldehyde ?
(A) CH 3CO Cl
(D) CH 3 CH Cl2
48.
50.
51.
(A) CH 3 I + ( CH 3 )2 CHO -
(B) CH 3 I + ( CH 3 )2 CHOH
(C) ( CH 3 )2 CHI + CH 3 O -
(D) ( CH 3 )2 CHCl + CH 3 OH
(B) CH 3 - O - C2 H5
(C) C2 H5 - O - C2 H5
(D) ( CH 3 )2 CH - O - CH ( CH 3 )2
52.
Which of the following reagent is used to convert Butan-2-one into propnroic acid
(A) NaOH, I
/H+
(B) Fehling Solution
2
(C) Tollen's reagent
(D) NaOH, NaI/H+
53. By which of the following proceducres can ethyl n-propyl ether be obtained ?
H O
HBr
Mg
Na
I
II
III
(A) C2 H5OH
ether
C H Br
2
1.CH O
HBr
Mg
Na
I
II
III
(B) C2 H5OH
ether
C H Br
2.H O
2
140 C
(C) C2 H5OH + H 2SO 4
180 C
I
(D) C2 H5OH + Conc H 2SO 4
CH CH CH Br
3
182
54.
60.
61.
(B) H2/Ni
HO
O
CH 3
CH 2 CH 3
HO
(C) NH 2 NH 2 , OH -
(D) NaBH 4
CH 3 - CHO + HCN
A, compound A on hydrolysis gives
(A) CH 3 - CH 2 - COOH
(B) CH 3 - CH 2 - CH 2 - NH 2
(A) propan-1-ol
(C) ethanoic acid
(B) propan-1-amine
(D) propanal
62.
A compound, containing only carbon, hydrogen and oxygen, has a molecular weight of 44. On complete
oxidation it is converted in to a compound of molecular weight 60. The original compound is
(A) an aldehyde
(B) an acid
(C) an alcohol
(D) an ether
63. The major organic product formed from the following reaction
O
CH NH
(i)
..... is
3
(ii) LiAlH4
(iii) H2O
183
H CH 3
N
OH
(A)
(C)
O NHCH 3
(B)
H
N CH 3
(D)
N CH 3
H
OH
64.
65.
A Compound containing molecular formula C5 H10Cl2 on hydrolysis gives compound cotaining molecular
formula C5 H10O , Which reacts with NH 2OH and also forms iodoformbut does not give fehling test
Original compound is
(A) CH 3
Cl
|
- C - CH 2 - CH 2 - CH 3
(B)
CH 3
Cl
|
- CH 2 - C - CH 2 - CH 3
|
Cl
|
Cl
Cl
|
(C) CH 3 - CH 2 - CH 2 - CH 2 - CH
(D) CH 3 - CH - CH - CH 2 - CH 3
Cl
Cl
Cl
66.
184
69.
70.
OH
OCH - CHO
HOH 2 C - COOH The reaction given is
71.
74.
(D) CH 3COCH 3
Carboxcylic acids are more acidic than phenol and alcohol because of
(A) intermolecular hydrogen bonding
(C) highly acidic hydrogen
73.
(C) HCHO
O
O
O
||
||
||
CH
C
H
CH
C
- CH 3
ph
C
ph
3
3
The correct order of reactivityof phMgBr with
,
,
( II )
(III)
(I )
(A) I > II > III
72.
(B) CH 3CHO
(B) CH 2 = CH - CH 2OH
(C) CH 3 CO C6 H5
(D) CH 3 - CH 2 - CHO
75.
76.
77.
(A) CH3-C(OH)-C6H5
(B) CH3-CH(OH)-C2H 5
(D) CH3COC6H5
(D) CH3CH(OH)C6H5
Among the following acids which has the lowest pka vulue
(A) CH 3COOH
(B) HCOOH
(C) ( CH 3 )2 CH - COOH
(D) CH 3 CH 2 COOH
(B)Aldol condensation
(C)Reimer-Tiemann reaction
(D)Cannizzaro reaction
(B) Ag(NH3)2+
(C) HNO2
185
(D) I2
78.
79.
80.
81.
Ethanal is treated with excess of ethanol in the presence of hydrochloric acid. The product is
O
||
(A) CH 3 - CH 2 - CH 2 - C - CH 3
OH
(B) (CH3)2C OC H
2 5
O
||
(C) CH 3 - CH 2 - CH 2 - C - CH 2 - CH 2 - CH 3
(D) CH 3 C
H
82.
OC2H5
OC2H5
50% KOH
Cl
(A)
(B)
Cl
OH
OH
COO
CH2OH +
(C)
OH
CH2OH +
Cl
Cl
83.
CH2COO
CH2OH +
COO
CH2OH +
(D)
OH
Cl
OH
OH
HO
(A) 1
(B) 2
OH
OH
(C) 3
186
(D) 4
84.
85.
86.
(B)pinacols
(C)alcohols
(87) In the presence of a dilute base, C6 H 5CHO and CH 3CHO react together to give ______
product.
(A) C6H5CH3
(B) C6H5CH2CH2OH
(C) C6H5CH2OH
(D) C6H5-CH=CH-CHO
H SO
dilute
g
4
A
B. The compound B is ...
(88) CH CH
dil . H 2SO 4
NAOH
(A)
(B)
OH
OH
(C)
(D)
OH
(89)
CH 3
(C) CH3CH2COOH
187
(D) FCH2COOH
ANSWER KEY
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
B
A
D
B
D
B
D
B
C
C
A
A
C
D
B
C
B
A
A
C
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
D
A
D
A
B
C
D
B
D
B
B
C
C
C
D
C
C
A
A
C
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
B
A
D
A
D
C
D
B
A
D
C
A
B
D
C
A
C
B
B
D
188
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
C
A
C
B
A
C
D
D
B
B
C
D
B
A
B
D
B
B
B
B
81
82
83
84
85
86
87
88
89
90
D
C
C
D
B
B
D
A
B
C
CH3
|
H5C2 N C CH2 CH3
|
|
CH3 C2H5
2.
3.
4.
5.
6.
7.
R - X + NH 3
(C)
H
R - CN + H 2 O
Na
(B)
C2 H5 OH
R - CH = N.OH + [ H ]
(D)
4
R - CONH2
LiAlH
Which of the following amides will not undergo Hofmann bromamide reaction ?
(A) Ethanamide
(B) Propanamide
(C) Benzenamide
(D) Acetanilide
Which of the following represents the poisonous gas which caused Bhopal tragedy in 1984 ?
(A)
CH 3 - N = C = O
(B)
CH 3 - N = C = S
(C)
CH3 - CH = N = S
(D)
CH3 - O - N == S
Choose the proer option for given statement on the basis of physical properties
Statement : (i)
Alkyl isocyanides have bad odours while alkylcyanides have pleasant odours.
Statement : (ii)
Alkyl cynanides are poisonous compounds.
Statement : (iii) The boling points of alkyl cyanides are lower than their isomeric alkyl-isocynides.
Statement : (iv) Acetonitrile is soluble in water but methylcarbylamine is not.
(A) TTTF
(B) TFTF
(C) TFFF
(D) TFFT
Phenyl isocyanide is prepared by which of the Following reaction ?
(A) Hoffmann reaction
(B) Carbylamine reaction
(C) Reimer-Tiemann reaction
(D) Wurtz reaction
What is the end product (B) in the following reaction sequence ?
P2O5
LiAlH 4
Butanamide
A
B
D
(A)
(C)
n - butylamine
Propyl isocyanide
189
(B)
(D)
n - propylcyanide
n - Propylamine
8.
(A)
R 2 C = N.OH
(C)
|
R - C = N.OH
(D)
R 2N - N = O
R 2 C - NO 2
(B)
9.
|
NO
Cl2 / NaOH
excess
[]
HNO
CHCl3
(A)
ClCH 2 NO 2
(B)
CH 3Cl
(C)
Cl 2 CH NO 2
(D)
Cl 3CNO 2
10.
Which of the following amines can not be Prepared by Gabriel - Phthalimide reaction ?
(A) Benzylamine
(B) Ethylamine
(C) Aniline
(D) Methylamine
11.
In (CH 3 )3 N the state of hybridization of N-atom and the Spatial rearrangement of methyl groups
around it are respectively.
12.
(A)
SP 3 , Pyramidal
(B)
SP 3 , tetrahedral
(C)
SP 2 , trigonal planar
(D)
SP 3 , trigonal planar
Which of the following Compounds loses optical activity due to nitrogen inversion ?
(A)
CH 3CH 2 CH CH 3
|
NH 2
(C)
CH 3CH2 CH2
13.
CH
CH2 CH3
3s
+
N CH 2 CH = CH 2 I
|
CH 3
CH 2 C6 H 5
|
The pKa Values of same bases are given below pick out the weakest base.
(A) 4.40
(B) 4.00
(C) 2.88
(D) 10.68
190
14.
15.
16.
17.
(B)
(C)
(B)
(C)
(D)
NaNO2 + HCl
H / H 2O
CuCN / KCN
C6 H 5 NH 2
x
y
z
273 K
Boil
18.
(A)
C 6 H 5CN
(B)
C 6 H 5CONH 2
(C)
C 6 H 5COOH
(D)
C 6 H 5CH 2 NH 2
19.
20.
NH2
NH2
(B) CH3O
NH2
(D) CH3
NH2
H 3 PO 3
(B)
H 3 PO 4
(C)
H 3 PO 2
(D)
HPO 3
Which prouduct will be obtained by the hydrolysis of the product obtained by reaction of butane nitrile with Ethyl magnesium bromide ?
(A) Ethyl - n - propyl ether
(B) Ethoxy propane
(C) Ethyl propanoate
(D) Hexan - 3 - One
191
21.
Which of the following daizonium salts when boiled with dil. H 2SO 4 gives the corresponding phenol
most difficult ?
(A) HO3S
22.
23.
N+ N
(C) Br
N+ N
(D) CH3O
N+ N
Arrange the following amines in order of increasing basicity n - pentylamine (I), Sec-pentyl amine
(II), iso - pentylamine (III), tert - pentylamine (IV).
(A) I < II < III < IV
(B) II < III < I < IV
(C) IV < III < II < I
(D) III < IV < I < II
Match the entries of column - I with appro priate entries of column - II and choose the correct
option.
Column - I (Amine)
24.
25.
26.
N+ N
(B) CH3
- Cloumn - II
(A) Benzenamine
- (P)
(B) N - Methyl aniline
- (q)
(C) N, N - di Methylaniline
- (r)
(D) N - Ethyleethanamine
- (s)
(A) A-P, B-q, C-r, D-S
(B)
(C) A-S, B-P, C-q, D-r
(D)
Which of the following statement is correct ?
(A) P - nitroaniline is a stronger base than aniline.
(B) Aniline is a weaker base than O-methoxyanline
(C) P - methoxy aniline is a weaker base than aniline
(D) Aniline is a weaker base than ethylamine
Benzylamine may be preared by.............
( P K a Value)
11.0
5.08
4.30
4.62
A-q, B-p, C-r, D-s
A-S, B-r, C-q, D-P
(A)
LiAlH 4 / ether
C6 H5CONH 2
(B)
LiAlH 4 / ether
C6 H5CN
(C)
( iii ) Aq NaOH D
(D)
AC 2 O
Br2
2O
(B) H
(C)
P-toludine (A ) CH
COOH
H+
3
COCH3
Br
NH2
COCH3
(A)
(B)
CH3
(C)
CH3
NH2
Br
CH3
192
(D)
NHCOCH3
Br
CH3
27.
28.
29.
The correct order of decreasing basic nature for the bases NH 3 , CH 3 NH 2 and (CH 3 ) NH is....
(A)
(B)
(C)
(D)
When a primary amine reacts with chloroform in ethanolic KOH, then the product is............
(A) an isocyanide
(B) an aldehyde
(C) a Cyanide
(D) an alcohol
In the following sequence of reactions, what are suitable for (A) and (B) when (D) is 1 - phenyl
propan - 1 - one.
Hydrolysis
D + Mg(NH2)Br
A + B [ C ]
+ H 2O / H +
30.
31.
32.
(A)
(B)
(C)
A = CH 3CH 2 - C N, B = C6 H5 MgBr
C 6 H 5OH
(B)
CH 3 NH 3+ Cl -
(C)
CH 3 - C CH
(D)
C 6 H 5CH 2 OH
193
33.
34.
35.
36.
Statement - 1
Aniline on reaction with at NaNO2/HCl 273K following by coupling with b-naphthol gives a dark
red coloured precipitate.
Statement - 2
The colour of the compound formed in the reaction of aniline with NaNO2/HCl at 273K followed
by coupling with b-napthol is due to the extended conjugation.
Statement - 1
Primary aliphatic amine forms highly stable alkyl diazonium salt.
Statement - 2
Benzenediazonium chloride is easily soluble in water while Benzene diazonium fluoroborate is insolubel
in water.
Statement - 1
Aniline is a weaker base than ammonia
Statement - 2
Aniline is resonance stabilized.
Statement - 1
P - nitro anline is a weaker base than p-toludine
Statement - 2
The electron with drawing - NO 2 group in P-nitroaniline makes it a stronger base.
37.
38.
Statement - 1
"Benzonitrile can not be prepared by nucleophilic substitution of benzene".
Statement - 2
" Benzonitrile can be easily prepared via diazonium salt".
Statement - 1
" Carboxylic acids are obtained by hydrolysis of Cyanide compounds in presence of sulphyric acid
and ammonia is liberated."
Statement - 2
" Primary amine is obtained by reduction of cyanide compound in presence of LiAlH4 . "
39.
40.
Statement - 1
"Gabriel Synthesis is used in the preparation of primary alifatic amines."
Statement - 2
"Primary aromatic amine can be prepared by Gabriel synthesis's method."
Statement - 1
" The boiling points of alkyl isocyanides are lower than their isomeric alkyl cyanides."
Statement - 2
"Isocyanide group is polar, so its boiling points is higher than their isomeric alkyl cyanides."
194
41.
42.
An organic compound (A) on reduction gives compound (B) on treatment with CHCl 3 and alcoholic
KOH gives (C) on Catalytic reduction gives N - Methyl aniline. The compound (A) is........
(A) Methylamine
(B) Aniline
(C) Nitrobenzene
(D) Nitro methane
Which is formed when (CH3)4 N OH is heated ?
(A)
CH 3 NH 2
(B)
C 2 H 5 NH 2
(C)
(CH 3 )3 N
(D)
(CH 3 )2 NH
43.
Aniline first react with acetyl chloride producing "A". "A" reacts with nitric acid / sulphuric acid
mixure and produce compound "B", which hydrolyses to compound "C" what is the identity of "C"
?
(A) Acetanilide
(B) P - nitro aniline
(C) P - Nitroacetanilide
(D) Sulphanilic acid
44.
Statement : (1) Sulphonation of aniline with conc. H 2SO 4 at 455 - 475 gives sulphanilic acid
45.
CN
46.
H O
+ CH3MgBr Q
P The procut "P" in the above reaction is ...........
OCH3
3
CH
(A)
47.
48.
OH
CH3
COCH3
CHO
(B)
OCH3
(C)
OCH3
OCH3
COOH3
(D)
OCH3
(A)
(C)
Toluene
Benzaldehyde
(B)
(D)
195
Benzyl alcohol
Benzene diazonium chloride
49.
In the following reaction sequence, predict the compound (x) and (y).
NH2
( i ) NaNO2 / HCl
Exless Br2
273 K
x
Y
( ii ) H 3 PO2
CH3
NH2
(A)
Br
Br and CH
3
(B) Br
CH3
(C)
NH2
Br
Br
Br
and
Br
NH2
Br and
(D)
Br
Br
CH3
CH3
NH2
Br
Br
Br
Br
Br
OH
and
CH3
CH3
50.
How many primary amines are possibile with the formula of C 4 H11 N ?
51.
(A) 1
(B) 2
(C) 3
Which of the following is not the correct reaction of aryldiazonium salts ?
52.
(A)
HCl
C6 H 5 N 2+ Cl - + CuCl
C6 H 5 Cl
(B)
D
C6 H 5 N 2 + Cl - + HBF4
C6 H 5 F
(C)
C6 H 5 N 2+ Cl - + H 3 PO 2
C6 H 5 PO 4
(D)
C6 H 5 N 2+ Cl - + SnCl2 / HCl
C6 H 5 NHNH 2
(D)
9s and 3p
(B)
9s and 9p
(C)
3s and 4p
(D)
5s and 7 p
53.
54.
55.
Br
N2
(B)
H2
(C)
C2H 2
(D)
CO 2
When primary amine is heated with CS2 in presence of excess of HgCl 2 , it gives isocyanate The
reaction is called :
(A) Hoffmann's bromamide reaction
(B) Perkin's reaction
(C) Hoffmann's mustard oil reaction
(D) Carbylamine reaction
196
56.
Br2
Acetamide
KOH
(B)
(C)
57.
Ethanenitrile LiAlH
4
(D)
Acetamide LiAlH
4
58.
59.
60.
61.
62.
63.
64.
65.
CH3
(B)
NH2
NH2
NH2
(C)
CH3
(D)
CH3
66.
NHCONH2
NHCOCH3
(A)
(B)
Br
NH2
OH
(C)
(D)
Br
Br
67.
68.
(A) Hexanamide
(B)
(C) Heptanamide
(D)
Identify A, B, C and D in the following reactions :
Br
NH2
Pentanamide
Butanamide
Br2
NaNO2 / HCl
H 3 PO2 / H 2O
Sn / HCl
C
B
Nitrobenzene
D
A
273 K
Excess
(A)
69.
A = aniline, B = 2, 4, 6 - Tribromoniline,
C = 2, 4, 6 - tribromo benzene diazonium chloride
D = 1, 3, 5 - tribromo benzene
(B) A = Benzene, B = 2, 4, 6 tribromo benzene
C = 2, 4, 6 - tri chloro benzene
D = 2, 4, 6 - tri chloro phenol
(C) A = aniline, B = P-bromoaniline, C = P-bromobenzene diazonium chloride.
D = P - bromo phenol
(D) A = aniline, B = p-bromo aniline, C = p-bromobenzene diazonium chloride.
D = Bromo benzene
Identify A, B and D in the following reaction :
CH3CH2CH2NH2
70.
71.
PCl5
Na1C2 H 5OH
KCN
HONO
D
B
C
(A)
[A] = CH 3CHO,
[B] = CH 3Cl,
[D] = CH 3CH 2 NH 2
(B)
(C)
(D)
[A] = CH 3CHO,
198
72.
73.
(A)
74.
75.
76.
77.
78.
79.
80.
81.
82.
(D) CH3 N CH 3
|
CH3
The number of possible structures of amines (C7H9N) having one benzene ring is..........
(A) 3
(B) 4
(C) 5
(D) 6
Number of primary amines of the formula C4H11N is .................
(A) 1
(B) 2
(C) 4
(D) 3
The reagents needed to convert is/are : Benzenamide Acetanilide
(A) KOH/Br2, LiAlH4
(B) KOH/Br2, CH3COCl
(C) HONO, Cu2Cl2, (CH3CO)2O
(D) KOH/Br2, Ni/H2, CH3COCl
The compound C5H13N is optically active and reacts with HNO2 to give C5H11OH. The command
is
(A) N-methylbutanamine
(B) 1-amino pentane
(C) 2-Amino pentane
(D) N, N-Dimethyl propanamine
The amine which does not react with Acetyl chloride is
(C)
CH 2.NH2
(A)
CH 3 NH 2
(B)
(CH 3 )2 NH
(C)
(CH 3 )3 N
(D)
P-nitro aniline
Benzyl amine
( CH 3CO )2 O
Ni / H 2
NaCN
Chloro ethane
z Z in the above sequence is...............
x
y
(A)
CH 3CH 2 CH 2 NHCOCH 3
(B)
CH 3CH 2 CH 2 NH 2
(C)
CH 3CH 2 CH 2 CONHCH 3
(D)
CH 3CH 2 CH 2 CONHCOCH 3
Aniline when diazotized in cold and then treated with Aniline gives a coloure product, Its structure
would be.......
(A) CH3
N=N
NH2
(C) H2N
N=N
NH2
(B) H2N
7
(D)
199
(B)
(D)
N=N
N=N
Aniline
Benzylamine
83.
84.
85.
(A)
( i ) Br2 , KOH
?
( ii ) Heat
O
O
(B)
( C)
NH
86.
87.
88.
(B) H3C
NC
(D) H3C
O
O
CN
(A)
89.
NCO
(D)
NH
CH3
|
N NO2
NHCH3
NO
(B)
NHCH 3
+
(C)
OH
|
N CH3
(D)
CH3
|
NN=O
NO
Suggst a structural formula of a compound having molecular C8 H11 N(A ) Which is optically active
dissolves in dil aqueous HCl and releases N 2 with Nitrous acid.
NH2
NH2
(A)
(B)
CH2CH3
90.
NH2
CH3
(C)
CH3
(D)
H3C
CH3
CH CH3
|
NH2
Which is the oxidised product of when benzene diazonium chloride treated with hypo
phyosphrous acid ?
(A)
H 3 PO 4
(B)
H3PO 3
(C)
200
H 4 P2 O 7
(D)
None of this
91.
Re d n
[0]
NaNO2 / HCl
Br2
H 2O , H 3 PO2
Sn / HCl
E
A
B
C
D
KMnO4
Bromination
273- 278 K
NO2
Soda lim e
F
D
92.
(A) Benzene
(C) Bromobenzene
(B) 1,2-dibromobenzene
(D) 1,-2 - dibromobenzoicAcid
Give the IUPAC name of product (A) and (D) respectively.
D
- BF3
+
C 6 H5 N 2 Cl- + HBF4
NaNO2 ( aq )
Cu ,D
- NaBF4
- N2
93.
- N2
Ni / H 2
AC2 O
B
C
D
- CH3COOH
Reduction
NaNO2 + HCl
3
Zn kkWzh
CuCN / KCN
Ni/3H 2
Con . H 2 SO4
D
C 6H 5OH
A
E
C
273 K
D
B
Con . HNO3 /
( NaOH + CaO )
H / H 2O
Con . H 2 SO4
G
F
H
D
94.
95.
OH / NaOH
OH / NaOH
(C)
NH2 / HCl
(D)
CH3
CH3
/ HCl
(A)
A - P, B - Q, C - R , D - S
(C)
A - Q, B - P, C - R , D - S
(B)
A - R , B - S, C - A, D - Q
(D)
A - S, B - Q, C - P, D - R
96.
97.
Which of the following subsance gives reaction with benzene sulphonyl chloride ?
(A) N, N - Dimethyl ethanamine
(C) Methyl ethylamine
(B) Trimethylamine
(D) Dimethyl ethyl amine
Identify, (A), (B) and (C) for the reaction given :
H 3 PO4
A + H 3 PO3 + HCl
+ H 2O
SnCl 2 + HCl
B + HCl
C6H5N2+Cl
dil . H 2 SO4
C + N 2 + HCl
> 283 K
NH-NH2
(A) A =
,B=
98.
,C=
(B) A =
,B=
NH-NH2
,B=
Cl
OH
(C) A =
NO2
OH
OH
,C=
NH-NH2
,C=
(D) A =
OH
,B=
,C=
99.
(B)
(D)
(A) H2N
(C) H2N
OCH3
(B) H2N
CH3
C6 H5 N 2+ Cl - + HBF4 C6 H5 N +2 BF4 -
C6 H 5 F
(B)
3 + 3 KOH
C 6 H 5 - NH 2 CHCl
C 6 H 5 - N + C -
(C)
C 6 H 5 - N +2 Cl - Cu
- Powder
C 6 H 5 - X + N 2 + CuCl
(D)
4 NaOH
C 6 H 5CONH 2 Br
2 +
C 6 H 5 - NH 2 + Na 2 CO 3 + 2 NaBr + 2H 2 O
HX
R 2 NH
(B)
R 3N
(C)
R - NH 2
(D)
NH 3
202
NH2
CH = CHNO2
102.
Zn / Hg
COCH3
CH = CH.NO2
CH2CH2NH2
CH = CH.NH2
(A)
(B)
CH2CH3
CH2CH2NO2
(C)
(D)
CH2CH3
CH2CH3
CH2CH3
103. Which of the following statement is true regarding the basicity of the following two primary amines ?
CH2NH2
CH2NH2
I
(A)
(B)
(C)
(D)
II
O
|| ..
+ ..
104. R C CH N N Intermediate + N 2
4
CH 3COOH
[A]
( i ) KCN
( ii ) LiAlH 4
[ B]
Carbanion
Freeradical
-
CHCl3 / OH
[ C]
LiAlH 4
(A)
CH 3CH 2 OH
(B)
CH 3CH 2 CH 2 NH CH 3
(C)
CH 3CH 2 CH 2 NH 2
(D)
CH 3 CH 2 CH 2 COOH
106. Which of the following can undergo Hofmann reaction most easily ?
CONH2
(A)
(B)
(C)
SO3H
(D)
OCH3
CONH2
CONH2
CONH2
Acrylonitrile
Prop - 2 -ene nitnle
(B)
(D)
203
Vinyl Cyanide
All are correct
NO2
Methyl isocyanide
Methyl carbylamine
(B)
(D)
ethane isonitrile
both (a) and (c)
ANWER KEY
1.c
2.c
3.d
4.a
5.d
6.b
7.a
8.c
9.d
10.C
11.a
12.c
13.c
14.c
15.b 16.b
17.c
18.a
19.c
20.d
21.a
22.c
23.d 24.d
25.d
26.c
27.d
28.a
29.d 30.d 31.b
32.a
33.c
34.d 35.b
36.c
37.b 38.b
39.c
40.a
41.c
42.c
43.b 44.d
45.d
46.c
47.d 48.b
49.b 50.d
51.c
52.a
53.a 54.b 55.b
56.c
57.b
58.a
59.c
60.d
61.c
62.a 63.b 64.d
65.a 66.d
67.a
68.a
69.c
70.b
71.c
72.a
73.c
74.c
75.c
76.b
77.c
78.c
79.d
80a
81.b 82.d
83.c
84.a
85.c
86.c
87.c
88.d
89.d 90.b
91.c
92.d
93.d 94.b 95.d
96.c
97.a
98.c
99.c 100.a
101.a 102.b 103.d 104.c
105.b 106.c 107.d 108.d
204
Hints
8.
HONO
R C NO2
R - CH2NO2
- H 2O
||
Nitro
NOH
Compound
Nitrolic acid
9.
10.
Primary aromatic amine can not be prepared by this method because nucleophile aryl halide,
does not become favouable anion for phthalimide.
12.
Due to nitrogen inversion 3o - amines with three different alkyl groups undergo racemization
hence lose optical activity i.e, option (C) is correct.
13.
Kb = 14
P Kb
= - log Kb
For,
option (C) P K b = 2.88 hence, P K b =14 - 2.88
P Kb
14.
= 11.12
15.
16.
3 > 2o > 1o
Only aromatic primary amines gives dye test.
18.
Due to strong electron -withdrawing effect of the - NO 2 group, the nucleophilicity of the
22.
As the steric hindrance increases from (I ) + (IV ) the basicity decreases, so, increasing order of
basicity becomes IV < III < II < I.
31.
CH 3 NH 3+ Cl - being asalt, undergoes almost complete dissociation, therefore, it has a high dissociation
constant.
NO2
41.
(A)
Nitrobenzene
Re d
NH2
CHCl3/ KOH
(B)
+
NC
(C)
205
H 2 Catalyst
Re d n
NH CH3
N - methylaniline
42.
D
[ (CH 3 )3
(CH 3 )4 . N. OH
NH2
43.
N ] + CH 3OH
NHCOC6H5
CH3COCl
HCl
Aniline
HNO3 +
Conc.H2SO4
288 K
Acetanilide
NH2
NH 2
+
NO2
p - Nitro
aniline
NH2
45.
NHCOCH3
NO2
NHCOCH3
+
o - Nitroace
tanilide
NO2
p - Nitroace
tanilide
H+ / H2 O
NO2
CH3COOH
o - Nitro
aniline
NHCOC6H5
C6H5COCl
HCl
Aniline
Benzanilide
50.
52.
CH 2 = CH - CH 2 - N + C - (allyl isocyanide)
54.
2C 2 H 5 NH 2 + 2 Na 2C 2 H 5 NHNa + H 2
55.
58.
R - NH 2 + HNO 2 R - OH + N 2 + H 2 O
59.
Aliphatic amine
Alcohol
(i)
( ii )
CH 3CH 2 CH 2 NH 2
Propan -1-amine
(iv)
CH3 - CH - CH3
|
NH 2
Propan - 2 - amine
( iii )
C2 H5 - NH - CH3
N-mthyl ethanamine
(CH 3 )3 N
N, N - dimethyl Methanamine
62.
73.
Gabriel phthalimide reaction is used for the preparation of primary aliphatic amines only.
206
74.
NH2
CH3
NH2
CH3
(i)
75.
(ii)
NH2
CH3
(iii)
NHCH3
CH2NH2
(iv)
(v)
CH3
|
CH3 C CH3 ,
|
NH2
(ii)
(iii)
(iv)
77.
It has chiral carbon
So, it is optically active.
78.
3o - amines do not react with acetyl chloride because they do not have replaceable H atom.
79. Benzylamine is stranger base because the lone pair on N atom is not de localised over the benzene
ring.
88. Secondary aliphatic and aromatic amines react with nitrous acid to form N - nitroso amine.
102. Amalgamated Zn and HCl reduces carbonyl group to methylene group without affecting double
bond.
- Co - - CH 2 -
103.
II
b-Carbon
3
SP hybridisation
O
|| ..
+ ..
104. R C CH N N
CH2NH2
b-Carbon
2
SP hybridisation
N2
O
|| ..
R C CH
Carbene
106. - OCH 3 is more electron - releasing hence when the migrating aryl group has - OCH 3 in the para
position, its migrated is accelerated.
207
Unit-25 - POLYMER
IMPORTANT POINTS
INTRODUCTION
Polymer : Polymer (poly = many ; meros = parts) : is defined a material which is made by linking
together a large number of small recurring units called monomers. For example, polythene
(CH2 CH2 )n is formed by linking together a large number of ethene (C2H4) molecules.
Difference between Polymer and Macromolecule. Both polymer and macromolecules are
very big molecules. In a polymer there must be repeating units. But in a macromolecule, the
repeating unit may or may not be present. For example, polyethene containing the repeating unit
CH2 CH2 - , is regararded as both a polymer and a macromolecule. But chlorophyll having
formula C55H72O5N4Mg does not have any repeating unit and hence it is known as a macromolecule
but not a polymer.
CIASSIFICATION OF POLYMERS
(i) Cassification Based on Source
Natural and Synthetic polymers. The polymers found in nature are known as natural polymers
which control the life process in plants and animals and known as biopolymers, e.g., starch,
cellulose, proteins and nucleic acids. The polymers which are made in the laboratories are
known as synthetic polymers e.g., polythene, nylon, dacron etc.
Semi-synthetic polymers. Semi synthetic polymers are chemically modifiend naturally occurring
polymers. e.g., semi synthetic cellulose diacetate fibers are obtained by acetylation of nautural
celllose whith acetic anhydride in persence of sulphuric acid. An explosive cellulose nitrate
obtained obtained on nitration of cellulose is another example of semi-synthetic polymer Vulcanised
rubber used for making rubber tyres is also a semi-synthetic polymer.
(ii) Classification based on Polymerisation reaction
Polymerisation. I is the union of two or more of smaller molecules of similar or different type with
or without elimination of a small molecule like water, HCl etc., resulting in the formation of a new
C C bond.
The number of repeating units (n) which link together to forma molecule is known as the degree of
polymerisation.
(iii) Classification Based on Mode of Polymerisation
Chain growth polymers. These polymers are formed by successive addition of monomer units to
the growing chain having a reaction intermediate (free radical, carbocation or carbanions) at one end
of the chain. Chain growth polymers are formed by a process which involves chain reactions and
the process is called chain gorwth polymerisation.
Step growth polymers. These polymers are formed through a series of independent steps (reactions).
Each step involves the condensation (bond fromation) between two bifunctional units (monomers)
leading to the formation of a dimer, trimer, tetramer etc. Since the polymer is formed in a stepwise
manner, the process is called step growth polymerisation.
208
Some important differences between chain growht and step growth polymerisaion are given
below :
Sr. Chain growth polymerisation
Step growth polymerisation
No.
(i) Addution polymerisation.
Condensation polymerisation.
(ii) Monomers add to growing chain.
Monomers add in steps to from dimers, timers.
(iii) Takes place through chain reactions
Takes place through condensation reaction
in the presence of initiators.
(iv) Fast reaction
Slow reaction.
(b) Homopolymer and copolymer
Homopolyme. If a polymer is made up of identical monomers, it is a called a homopolymer (......M-M-M-M.......). For example, polythene, polyvinyl chloride and neoprene.
Copolymers. If a polymer is made of monomers of different chemical structures, it is caled a
copolymer (...... M1 M2 M1 M2 .......). For example Buna-S, butyl rubber and nitrile
rubber.
Copolymerisation is the polymerisation of two or more different monomer species resulting in high
molecular mass compounds called copolymerisation.
(c) Addition and condensation polymers
Addition Polymerisation. In this process, the simple monomers are joined together without loss of
molecules like H2O, NH3, etc. Polythene is one example.
Condensation Polymerisation. In this process, the simple monomers are combined together whith
the loss of simple molecules like H2O, NH3, etc., e.g., nylon.
Some important differences between Additon and Condensation polymers are given below :
Sr. Addition polymers
Condensation polymers
No.
1. Formed by addition reaction.
Formed by condensation process with elimination
of small molecule like H2O.
2. Mol. mass is whole number multiple
Mol. Mass is not whole number multiple of
of Monomer.
the monomer units.
3. Generally involve one monomer Unit
Involve more than one monomer unit.
4. Monomers are unsaturated molecules. Monomer units must have two active functional groups.
5. They are generally chain growth
They are generally step growth polymers.
polymers.
(iv) Classification Based on Structure
Linear Polymers. In these polymers there are straight chains of polymer molecules. For example,
nylon and polyester. Linear polymers possess high melting points and high density.
Branched Chain Polymers. In these polymers there are braches along the chains of polymer
molecules. For example, amylopectin. Branched chain polymers possess low melting point and low
density.
Cross Linked polymers. In these polymers the linear chains are joinded together by a suitable
cross link and as a result a three dimentional network structure is formed. For example, polystyrene
butadiene polymer and urea formaldehyde polymer. The cross linking the mechanical strength also
increases.
209
durable materials are made from high degree polymers while lower degree polymers are used to
obtain soft and cheaper materials.
Modification in properties of polymer substances
The properties of the polymer substances can be modified to make them more useful by adding
certain substances to them. For example ;
(i) Inorganic substance like TiO2, BaSO4, CaCO3, SiO2, are added to the polymers to abrasion.
These additives are called fillers.
(ii) Organic substances like tricresyl phosphate, glyeryl phthalate, tertiary butyl phthalate, oleic acid
are added to some polymers to introduce softness. These additives are called plasticizers.
(iii) Organic substances like phenol, cresol, and quinol and carbon black are added to check the
effect of sun light on the polymers and to avoid their decomposition. There additives are called.
antiocidants.
Characteristics of polymer substances
(i) They are light in weight and many types of material can be made out of them.
(ii) They are not affected by atmosphere and moisture unlike wood, metal, leather, cotton clothes.
(iii) They are insulators and possess heat resisting property.
(iv) They are no affected by the germs and most of the chemicals.
(v) Their properties can be easily modified to meet the requirement.
(vi) Their raw materials are easily and cheaply available.
211
M.C.Q.
(1)
(2)
(3)
(4)
(5)
(6)
(7)
(8)
(9)
(10)
(11)
(12)
(13)
(14)
(15)
(16)
(17)
A high molecular weight molecule built from a large number of simple molecules is called a
(A) Monomer
(B) Isomer
(C) Polymer
(D) Tautomer.
A high molicular wieht molicule which does not contain repeating structural units is called a
(A) Polymer
(B) Macromolecule
(C) Both (A) and (B) (D) None of the above
The simple molecules from which a polymer is made are called
(A) Monomers
(B) Metamers
(C) Rotamers
(D) Eantiomers.
Which of the following is not a biopolymer ?
(A) Proteins
(B) Nucleic
(C) Cellulose
(D) Neoprene.
What is not true about polymers ?
(A) Polymers do not carry any charge
(B) Polymers hgave hig viscosity
(C) Polymers scatter light
(D) Polymers have low molecular weights.
On the bases of the mode of their formation the polymers can be classified
(A) as addition polymers only
(B) as condensation polymers only
(C) as copolymers
(D) Both as addition and condensation polymers
Natural rubber is a polymer of
(A) Butadiene
(B) Ethyne
(C) Styrene
(D) Isoprene
Terylene is a condensation polymer of ethylene glycol and
(A) Benzoic acid
(B) Phthalic acid
(C) Sakucylic acid
(D) Terephthalic acid.
Which one of the following is not an example of chain growth polymer ?
(A) Neopreme
(B) Buna-S
(C) PMMA
(D) Glyptal.
Which of the following is a synthetic polymer ?
(A) Starch
(B) Silk
(C) Protein
(D) Polystyrene.
Homopolymers are made from
(A) Only one type of monomers
(B) Two different of monomers
(C) Three different types of monomers
(D) Several different types of monomers.
Amongst the following, a homopolymer is
(A) PMMA
(B) Bakelite
(C) Glyptal
(D) Dacron
Which of the following is a copolymer.
(A) Buna-S
(B) PAN
(C) Polythene
(D) PTFE
Which of the following is a linear polymer ?
(A) Nylon
(B) Bakelite
(C) Alkyd resin
(D) Melamine-formaldehyde polymer.
Amongst the following, the branched chain polymer is
(A) PVC
(B) Polyester
(C) Low density polythene (D) Nylon-66
A copolymer of acrylonitrile and 1, 3-butadine is called.
(A) Buna-N
(B) Polystyrene
(C) Neoprene
(D) Buna-S.
Which of the following is wrong ?
(A) PMMA is called plexiglass
(B) PTFE is called teflon
(C) SBR is natural rubber
(D) LDPE is called low density polythene.
212
(18)
(19)
(20)
(21)
(21)
(22)
(23)
(24)
(25)
(26)
(27)
(28)
(29)
(30)
(31)
(32)
(33)
(34)
(35)
(36)
(37)
(38)
(39)
(40)
(41)
(42)
(43)
(44)
(45)
Natural rubber is
(A) Polyvinyl chloride (B) cis-Polyisoprene (C) trans- Polyisoprene (D) Polychloropene
Gutta percha is
(A) trans- Polyisoprene
(B) a synthetic polymer
(C) a very hard material
(D) All statement are correct
Natural silk is a
(A) Polypeptide
(B) polysaccharide
(C) polychloropene
(D) polyacrylonitrile
artificial silk is a
(A) Polypeptide
(B) polysaccharide
(C) polythene
(D) Polyvinyl Chloride
Which of the followin is not a polyamide?
(A) Wool
(B) Leather
(C) Nylon
(D) Natural rubber
Among the following polymer, the strongest intermolecular forces of attraction are present in
(A) Elastomers
(B) Fibres
(C) Thermoplastics
(D) Thermosetting polymers
Among the following the weakest interparticle forces of attraction present in
(A) Thermosetting polymers
(B) Thermoplastics polymers
(C) Fibers
(D) Elastomers
Thermoplastics are
(A) Linear polymers
(B) Soften or melt on heating
(C) Molten polymer can be moulded in desired shape
(D) All the correct
Which of the following is not a thermosetting polymer?
(A) Alkyd resin
(B) Bakelite
(C) Melmac
(D) SBR
Which of the following can be remelted time and again without producing any change
(A) Thermosetting polymers
(B) Thermoplastics polymers
(C) Bakelite
(D) Melamine-formaldehyde polymer
The tensile strength, elasticity and resistance to abrasion can be increased by a process called
........
(A) Diazotisation
(B) Vulcanization
(C) Isomerization
(D) Polymerization
The process of vulcanization was introduced by
(A) Charles goodyear (B) Kolbe
(C) Wohler
(D) Zeigler
Vulcanized rubber resists ........
(A) Wear and tear due to friction
(B) Cryogenic temperature
(C) High temperature
(D) Action of acids
The polymer obtained by condensation of sevacic acid and hexamethylenediamine is called .........
(A) Nylon-66
(B) Nylon-6
(C) Nylon-610
(D) Decron
The liner chains in nylon are held together by
(A) H-bonds
(B) Covalent
(C) Ionic bonds
214
(46)
(47)
(48)
(49)
(50)
(51)
(52)
(53)
(54)
(55)
(56)
(57)
(58)
(59)
(60)
(61)
(62)
(D) Sulphonation
(63)
(64)
(65)
(66)
(67)
(68)
(69)
(70)
(71)
(72)
(73)
(74)
(75)
(78)
(79)
(80)
(81)
(82)
(83)
(84)
(85)
(86)
(87)
(88)
(89)
(90)
(91)
(92)
(93)
(94)
(95)
(96)
(97)
(98)
(99)
(100) Ebonite is
(A) Natural rubber
(C) Higly vulcanized rubber
ANSWER KEY
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
C
B
A
D
D
D
D
D
D
D
A
A
A
A
C
A
C
D
D
C
D
D
D
C
D
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
B
A
C
D
B
D
D
A
B
D
B
D
D
D
B
B
A
A
C
A
C
A
B
D
B
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
218
A
C
A
A
B
D
A
C
B
C
C
B
A
C
B
D
B
A
D
C
A
A
B
A
B
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
B
D
C
A
D
B
B
D
B
A
D
A
A
C
D
A
A
A
A
B
A
C
B
C
C
UNIT - 26 - BIOMOLECULE
M.C.Q.
1)
is a biomolecule.
(A) protein
2)
(B) enzyme
(B) nucleic acid
(B) 1:1
15)
(C) tetrasaccharide
(D) polysaccharide
(B) 6,2
(C) 5,1
(D) 4,1
(B) soluble
(B) levoratatory
(C) (-)
(B) C2
(C) C3
(D) C4
(B) C2
(C) C3
(D) C4
(B) +52.50
(C) +66.50
(D) 1120
14)
(B) Trisaccharide
13)
(D) melitriose
12)
(C) fructose
11)
(B) dextrin
10)
9)
(C) oligosaccharide
Cyclic configuration for glucose is called Glucopyranose , because its cyclic chain contains
__________carbons & __________oxygens.
(A) 6,1
8)
7)
(C) 1:2
6)
(D) carbohydrate
5)
what is the proportion of hydrogen and oxygen in molecule of all member of carbohydrate ?
(A) 2:1
4)
is not a biomolecule.
(A) vitamin
3)
(C) lipid
(B) inversion
(C) diversion
(D) reversion
which optical rotation has been obtained by aqueous solution of sucrose mixture , which is
produced before hydrolysis of and after hydrolysis of sucrose ?
(A) Dextrorotatory , levorotatory
(B) C2-O-C2
(C) C1-O-C6
219
(D) C1-O-C2
16)
17)
(C) C 1-O-C 3
(D) C1-O-C 4
(B) maltose
(C) fructose
(B)16,173,74
(C) 16,74,173
(D) 173,74,16
(B) maltose
(C) lactose
(D) A & C
(B) maltose
(C) lactose
(D)A&B
(B) sucrose
(C) A&B
(D) none
(B) lactose
(C) A&B
(D) none
(B) maltose
(C) lactose
(B) maltose
(C) lactose
(B) maltose
(C)A&B
(D) none
(B) maltose
(C) lactose
(D) B&C
what is the specific rotation of aqueous solution of mixture , which is produced after hydrolysis of sucrose ?
(A) -200
33)
(B) C1-O-C 2
32)
31)
(C) maltose
30)
(B) fructose
29)
(D) arneto
which sugar reduces fehlings solution and makes phenyl hydrazone with phenyl hygrazine ?
(A) maltose
28)
(C) caramel
27)
(B) elitem
26)
(D) lactose
which substance is produced before obtaining alcohol from the compound containing starch ?
(A) sucrose
25)
(C) fructose
what are the sweetness index of fructose , glucose and lactose respectively
(A) 74,173,16
24)
(B) glucose
23)
22)
(C) sucrose
21)
(B) fructose
20)
(D) phosphosidic
19)
(C) phospholipid
18)
(B) glycosidic
(B) -92
(C) +52.50
(D) +66.50
The specific rotation in inverted sugar during hydrolysis due to specific rotation of glucose solution
is_______.(the mixture of glucose and fructose obtained at the end of hydrolysis is called inverted sugar )
(A) -200
(B) -920
(C) +52.50
220
(D) +66.5
34)
The specific rotation in inverted sugar during hydrolysis due to specific rotation of fructose solution
is_________ .(the mixture of glucose and fructose obtained at the end of hydrolysis is called
inverted sugar)
(A) -20
35)
39)
(B) starch
(B)sucrose
(C)maltose
(D) lactose
(B) sucrose
(C) maltose
(D) glucose
which substance in animal body can be Converted in glucose and also gives energy when
required ?
(B) glycogen
49)
(D) starch
(B) lilen
(C) rayon
(C) antibodies
protein is/are_________
(B) hormones
what are the names of scientist, who had obtained many amino acid from hydrolysis of protein ?
(C) Emil Fischer
(D) none
(C)upto 20000
(D) >10000
48)
(C) cellulose
(A) 100
47)
(A) alanine
46)
(C) protein
(D)C nH2nO n
(A) enzyme
44)
(B)C n+2H2nO n
(B)chloroform
(A) sucrose
42)
(D)A&C
(A)water
(A) starch
41)
(C) cellulose
(A)glucose
40)
(B)sucrose
38)
(D) +66.5
37)
(C) +52.5
example of polysaccharide is
(A)starch
36)
(B) -92
the polypeptide chains run parallel and are held together by _______bonds.
(A) disulphide
(B) covalent
(D) none
By which bond the polypeptide chains are held together in fibrous protein ?
(A) hydrogen bond (B) covalent bond
(D) A&C
50)
51)
(B) 48
(C) 60
(B) change in pH
55)
56)
(D) none
(D) all
in certain clynical chemistry tests removal of all protein materials , which chemical is added to
sample ?
(A) trichloro acetic acid
(D) apoenzyme
57)
(D) 72
(D) insulin
53)
(C) keratin
in a-helix shaped protein , polypeptide chain is coild in helix shape approximate_______ amino
acids are included per turn of helix
(A) 3.6
52)
(B) albumin
(C) CI, Br
(Active)
(Active)
(inactive)
(Active)
(Active)
(Active)
(C) emulsin
(D) lipase
(B) A
(C) C
(D) B
61)
(B) invertaze
60)
(B) phylloquinone
(C) Tocopherol
(D) retinol
62)
(Active)
59)
(inactive)
(B) pyridoxine
(C)thiamine
(D) Tocopherol
(C) B6
(D) all
(B) H
222
63)
64)
65)
(D) paralysis
purine base is
(A) G
66)
(C) C
(D) U
(C) U
(D)C
(B) G
(B)T
(B) C2
(B)C2
(B) Cl, C3
74)
76)
(C)C4
(C) C3, C5
(D) C5,C5
(D) all
by which bond , base of one nucleotide and base of another nucleotide are joined together ?
(C) coordination covalent bond (D) ionic
which pairs of bases are true for linkage between two chain of polynucleiotide ?
(A) adenine-Thymine
(C) guanine-thymine
(D) adenine-cytosine
how many hydrogen bonds between base G and Base C are present in structure of DNA ?
(A) 1
77)
(C)C3
(C) C4
73)
(C) C3
two nucleosides are joined together by phosphodiester linkage, this linkage is formed between
___________ of one sugar and ________ of other sugar.
(A) Cl ,C1
72)
(D) All
71)
(C) U
70)
(B) T
69)
(D) U
68)
(C) T
pyrimidine base is
(A) C
67)
(B) C
(B) 2
(C) 3
if a person bleeds by his gingiva , so what would you suggest to eat to prevent the disease ?
(A) vegetable oil
(C) cheese
223
(D) milk
78)
79)
(D) viatamine
(B) fructose
(C) maltose
(D) all
(B) lactose
(C) maltose
(D) none
(B) fructose
(C) galactose
(D) all
84)
(C) vitmin
83)
(B) vitamine
whichsugarisntindicatingmutarotation?
(A) sucrose
82)
(D) B12
81)
(C) B6
80)
(B) B4
(B) maltose
(C) A&B
(D)none
85)
one base present in central part of DNA, its joined to another base with 3 hydrogen bond, so
what is that base ?
(A)A
86)
(C)T
(D) U
one pyrimidine base present in central part of DNA, itsjoinedtoanotherbase with 2 hydrogen
bond, so what is that base ?
(A) A
87)
(B) G
(B) G
(C) C
(D) T
88)
the crystal of glucose obtained from which solvent are dissolved in water and the specific rotation
of this freshly prepared solution of glucose is +112 ?
(A) ethyle alcohol
89)
(C) pyridine
(D) A & B
90)
(B) aceticacid
(B) +52.5
(C) +112
(D) +119
91)
if the solution of glucose shows a specific rotation of +52.5 then mixture of a - D+ glucose ___%
and [a - D + glucose_______ %
(A) 25,75
92)
(C) aldohexos
(D) ketohexose
(B) sucrose
(C) maltose
(D) lactose
(B) 20,80
(C) 30,70
(D) 80,20
(B) C1-O-C 5
(C) C l-O-C 6
(D) C2-O-C 4
(B) C1-0-C4
(C) C1-0-C3
(D) C1-0-C6
99)
(B) ketopentose
98)
(D) ketohexose
97)
(C) aldohexos
96)
(B) ketopentose
95)
(D) 33,67
fructose is known______
(A) aldopentose
94)
(C)64,36
93)
(B) 36,64
(B) a-D+fructose
(D) b-D-glucose
(B) C l-O-C 3
(C) C l-O-C 4
(D) C l-O-C 6
(B) secondary
(C) tertiary
(D) A&B
(B) secondary
(C) tertiary
(D) A&B
(C)methionine
(D)all
(B)histidine
103) some amino acids are known as none essential aminoacid because
(A) they are not necessaryfor normal body reaction
(B) they are synthesized in body
(C) instead of those another amino acid are obtained through diet
(D) they cause disease in body
104) amino acid contains
(A) aminogroup
(D) A&C
105) in dry solid form the amino acid exists as dipolar molecule in which carboxyl group is present as
carboxylate ion & amino group is present as amonium ion this dipolar ion is also known
as_______ ion
(A) twitterion
(B) zwitterion
(C) carboxeminium
225
(D) all
106) in electric field the pH value at which amino acid doesnt migrate towards any electrode is
called______
(A) neutral point
(B) amphotericpoint
(C) isoelectricpoint
(D) all
(B) electrophoresis
(C) chromatography
(D) B&C
108) which bond is formed to reaction between amino group of 1-amino acid and carboxyl group of
another amino acid
(A) esterbond
(D) B&C
109) three different amino acids joined in different sequence to form different types of tri-peptide
(A)23
(B)33
(C)6
(D) 3
110) which ofthe followingsentence is true or false ? (symbol fortrue isT, and forfalse its F)
(i)
(ii)
group attached to Cl in cyclicstructure of glucose acts as reducing agent group, this glucose
is one monosaccharide unit of maltose
(iii)
(iv)
(A) FFTF
(B) FTTF
(C) TFFT
(D)TTTT
(B) amiloze
(D) B&C
(C) fructose
(D) A&B
(B) b-D+glucose
113) Answer, whether the following statements are true of false, & select properchoice !
(i)
(ii)
glycine got its name because it was first obtained from cheese
(iii)
(iv)
arginine is basicaminoacid
(v)
(vi)
(B) a-T,b-T,c-T,d-F
(C) a-F,b-T,c-F,d-T
(D) a-F,b-T,c-T,d-T
226
(d) (ii)-false,(ii,iv)-true
114) Amino acid is given in Column-1 & its nature is given in Column-ll so match the following
Column 1
Column II
i. lysine
a. acidic
ii. glysine
b. basic
iii. arginine
c. nutral
iv. alanine
(A) i-b,ii-c,iii-b,iv-c (B) i-b,ii-a,iii-b,iv-c
(C) i-a,ii-a,iii-b,iv-c
(D) i-c,ii-b,iii-a,iv-b
SECTION II
i. N-terminal residu
a.
b.
c.
d.
(A) i-a,ii-b
(B) i-c,ii-d
(C) i-b,ii-c
116) carbohydrate given in column I and its example given in column II, select proper choice
SECTION I
SECTION II
i. monosaccharide
a.
raffinose
ii. disaccharide
b.
fructose
iii. trisaccharide
c.
stachyose
iv. tetrasaccharide
d.
glycogene
v. polysaccharide
e.
cellobiose
(A) i-b,ii-e,iii-a,iv-d,v-c
(B) i-b,ii-e,iii-a,iv-c,v-d
(C) i-b,ii-d,iii-a,iv-e,v-c
(D) i-a,ii-b,iii-c,iv-d,v-e
117) chemical reactions are given in section I and chain or group present in structure of glucose are
given in section II. Match Section-I with Section-II
Section-I
Section-II
i.
ii.
c. OHC-C(OH)-C(OH)-C(OH)-C(OH)-CH2OH
chain is present
(C) i-d,ii-biii-a,iv-c
227
(D) i-b,ii-a,iii-d,iv-c
118) the observered angle of rotation of 6.25 g of sucrose in 25 ml of aqueous solution in a polarimeter
tube 15 cm long is +66.50 what is the specific rotation of solution of sucrose?
(A) 13.30
(B) 66.50
(C) 24.90
(D) 26.60
119) the observered angle of rotation of 20g of sucrose in 40 ml of aqueous solution in a polarimeter
tube 30cm long is +28.5, what is the specific rotation of solution of glucose ?
(A) 19
(B) 52.5
(C) 57
(D) 112
ii.
iii.
(A) FFT
(B) TTF
(C)TFT
(D) FTT
121) structure of protein given in column I, Shape & example of protein is given in Column II & its
bond isgiven in Column III, so match following,
COLUMN I
COLUMN II
COLUMN III
i.
primary structure
a. b- platinated
P. hydrogen bond
ii.
secondary structure
b. myoglobin
Q.disulphide bond
c. insulin
R. ionicbond
d. hemoglobin
S. vanderwalls force
(B) (i,ii,iv)
(C) (i,iii,v)
228
(D) (i,ii,iv,vi)
123) solubility of vitamin & sources are given in column-1 and vitamin isgiven in column II
COLUMN - I
COULMN II
i.
a. vitamin-A
b. vitamin-B
c. vitamin-C
d. vitamin-D
e. vitamin-E
f.
vitamin- H
g. vitamin-K
(A) (i-b,c) (ii-a,d,e,g) (iii-f) (iv-a) (v-d) (vi-g)
(C) (i-b,a) (ii-c,d,e,g) (iii-f) (iv-c) (v-a,d) (vi-e,g) (D) (i-f) (ii-a,d,e,g) (iii-d)(iv-d) (v-b,c) (vi-a)
124) Symbol of vitamin isgiven in column I, chemical name of vitamin isgiven in column II & disease
caused by their deficiency given in Column III, so match the correct answers
COLUMN I
COLUMN II
COLUMN III
i.
vitamin B6
a. ascorbic acid
p. bleeding in gingiva
ii.
vitamin A
b. pyridoxine
q. hair losses
iii. vitamin C
c. riboflavin
r. xerophthalmia
iv. vitamin H
d. retinol
s. convulsions
e. calciferol
t. beri-beri
f.
biotin
u. pernicious anemia
ii.
iii.
iv.
DNA is the exclusively responsible for maintaining the identity of different species of
organism upto 100 years
(A) TTFT
(B) FTFF
(C) FTFT
229
(D) FFFF
126) OH CH2OH
H
H
CH2OH
H
O
OH
H
OH
O H
OH
OH
OH
Structure P
Structure Q
(B)anomer
(C) enantiomer
(D) confirmer
CH2OH
H
OH
HOH2C
OH
OH CH2OH
H
OH
H
OH H
H
OH
OH
CH2OH
H
O
CH 2OH
OH
H
OH
OH
ii.
iii.
iv.
v.
vi.
133)
(B) FTTFTF
(C) TFFTFT
H
HO
OH
H
H
OH
HO
H
OH
(B) aldohexos
(C) b-furanose
(D) b-pyranose
231
'P'
OH
i.
(A) FTFFTF
'Q'
(D) TFFTTT
134) P is responsible for heredity & P is formed by Qand R. So give the name for P, Q and R.
(A) P = chromozomes Q = protein R = nucleicacid
(B)
COLUMN II
i.
ii.
Emil Fischer
iii.
ANSWER KEY
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
D
C
D
D
B
C
C
A
D
A
B
C
B
A
D
B
A
A
C
B
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
D
D
D
B
B
C
C
A
C
B
A
A
C
B
D
A
A
C
D
A
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
B
A
D
C
D
B
D
A
D
A
A
D
D
A
C
A
D
B
B
B
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
A
D
A
A
A
D
D
B
A
D
C
D
B
A
A
C
B
B
A
D
232
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
A
D
C
B
B
D
B
D
B
B
B
C
D
A
B
C
B
C
C
A
101
102
103
104
105
106
107
108
109
110
111
112
113
114
115
116
117
118
119
120
B
D
B
D
B
C
D
D
C
B
D
B
D
A
B
B
A
C
A
A
121
122
123
124
125
126
127
128
129
130
131
132
133
134
135
B
C
B
D
B
B
B
B
D
B
D
B
B
A
C
(A)
(B)
(D)
CONH2
12.
COCH3
11.
Cl
10.
(C)
NHCOCH3
CONH2
9.
Cl
OH
OH
[B] Analgesic
[C] Hypnotic
[D] Antiseptic
[D] Chemotherapy
[B] Typhoid
[C] Syphilis
233
[D] Cholera
13.
An antipyretic is
[A] Quinine
14.
16.
22.
[B] Antipyretic
[C] Sedative
[D] Psychedelic
[B] Monouretic
[C] Diuretic
[D] Triuretic
[B] LSD
[C] DDT
[D] TNT
[C] Diclofenac
[D] Morphine
[C] Chloroquine
[D] Paracetamol
[C] Antipyretic
[D] Anaesthetic.
[C] Pethidine
[D Bithional
Streptomycin is an example of
[B] Analgesic
[C] Dettol
28.
[D] Birthionol
[A] Soap
27.
[C] Norethindron
[A] Opium
26.
[B] Paludrin
[A] Antibiotic
25.
[D] Aspirin
[A] Aspirin
24.
[C] BHC
Aspirin is
[A] Codeine
23.
[B] TNT
[A] DNA
21.
[D] Sulphadiazine
[A] Uretic
20.
[C] Mescaline
[A] Antibiotic
19.
[B] Phenelzine
[A] Sulphaguanidine
18.
[D] Piperazine
Antiseptic chloroxylenol is
[A] Bakelite
17.
[C] Luminal
15.
[B] Paracetamol
[B] Bithional
[C] Cocaine
[D] Penicillin G
[C] Paracetamol
[D] Ampicillin
[B] Penicillin
234
29.
30.
32.
[D] Antipyretic.
[B] Luminal
[C] Phenol
[B] Antiseptic
[C] Analgesic
[D] Insecticide.
[B] Aspirin
[C] Penicillin
[D] Insulin.
[B] Lansoprazole
[C] Lysol
[D] Al[(OH)3
[C] Naproxin
[C] Terpineol
[D] Chloroform
What is the drug called which binds to receptor site and stop communication process of cell?
[B] Agonists
[C] pigonists
[D] logistic
44.
[C] Antiseptic
[A] Antagonists
43.
[B] Sedative
Drug which do not bind to the active site but bind to a different site?What is such site called ?
[A] Ranitidine
42.
[A] Equanil
41.
[B] Penicillin
[A] Omeprazole
40.
[D] Quinine
[C] Penicillin
[A] Quinine
38.
[B] Chloroquine
[A] Antipyretic
37.
[D] Vitamin
[C] Sulphanilamide
[A] Catechol
36.
[C] Hormone
[B] Sulphanilic acid
[A] Anaesthetic
35.
[B] Antipyretic
[A] Paracetamol
34.
[D] Quinine
[A] Aspirin
33.
[C] Paracetamol
Halinin is an
[A] Antibiotic
31.
[B] Novalgin
[B] meprombamate
[C] amytal
[D] Aspirin
[B] Chlorine
[C] KMnO4
235
[D] Phenol
45.
46.
[B] Aspirin
[C] Codein
[D] Heroin
47.
48.
[D] Phenol
49.
[C] Lysol
[D] Streptomycin
Dettol is a mixture of
[A] Chloroxylenol and terpeneol in a suitable solvent
[B] formaldehyde and phenol in the solvent water
[C] tincture of iodine and chloroform
[D] KMnO4 and iodoform
50.
51.
[D] morphine
[B] Dysentery
[C] Tuberculosis
[D] Diphtheria
[B] Dysentery
[C] Malaria
[D] Syphilis
[B] Pneumonia
[C] Diphtheria
[D] Malaria
[B] Dysentery
[C] Smallpox
[D] Syphilis
[C] Diphtheria
[D] Influenza
[C] sulphanilamide
58.
57.
[D] Xylocaine
56.
[C] Procaine
55.
[B] Cocaine
54.
[D] Xylocaine
53.
52.
[B] Cocainc
[B] Malaria
[B] piperazine
236
59.
60.
[B] piperazine
61.
[B] Veronal
[C] Reserpine
[D] Piperazine
62.
63.
[D] Streptomycin
[D] Streptomycin
[D] Chloramphenicol
67.
66.
[D] Cocaine
65.
64.
[B] Morphine
[D] piperazine
[A]
OCOCH3
COOH
NHCOCH3
[B]
CH3
[C]
Cl
[D]
CH3
OH
OH
68.
[A]
OCOCH3
COOH
NHCOCH3
OC2 H5
[B]
[C]
CH3
Cl
[D]
OH
OH
NHCOCH3
237
CH3
69.
OCOCH3
H2C
COOH
NH
[B] Piperazine HN
[A] Aspirin
H2 C
71.
NHCOCH3
A 16 years old boy came to the doctor with main complaints of frequent sneezing, watering from nose
and eyes, intense, itching in eyes. and cold. He has past history of allergy to dost. The doctor
prescribes most probably which of the drugs.
[A] Norediindrone
[B] Lansoprazole
The structure given below is known as
O
H2C
[C] Reserpine
NH2
[A] Penicilline F
COOH
H
[D] Penicillin K
[D] Ampicillin
[B] Saccharin
[C] Sucralose
[D] Alitame
74.
[B] Penicillin G
73.
[D] Chlorpheniramine
CH3
CH3
N
O
72.
CH2
NHNH2
[D] Paracetamol C2 H5 O
70.
CH2
[D] Saccharin
[C] Sucralose is 1600 times sweeter than sugar [D] Aspartame is 550 times sweeter than sugar
75.
76.
[B] DDB
[C] ABS
[D] CFRP
[C] Tetrazine
[D] Alitame
[B] Caramel
238
77.
78.
83.
[D] CH3[CH216
82.
[A] Reduces
81.
[D] Cl2
80.
[C] Bithional
79.
[B] KMnO4
[B] Cationic
[C] Non-ionic
[D] Biosoft
ANSWER KEY
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
C
D
A
A
A
A
C
B
C
D
B
C
B
B
A
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
C
C
B
C
B
C
C
C
A
D
C
C
A
A
A
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
C
A
B
B
B
C
B
A
C
A
A
A
D
D
B
239
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
C
D
C
A
C
A
D
B
A
D
C
D
D
C
D
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
D
A
B
D
C
C
A
B
D
D
B
A
A
B
A
76
77
78
79
80
81
82
83
D
C
A
C
A
B
B
A
Peliminary Test
(i)
Colour
Black
Blue
Orange
Salt
Oxides : MnO2 , FeO, CuO, Co 3 O4 , Ni2O3
Sulphides : Ag 2 S, CuS, Cu2 S, FeS, CoS, NiS , PbS, HgS , Bi2 S3 (blackish brown)
Hydrated CuSO4 , anhydrous CoSO4
KO2 ,
Green
Brownish
yellow
Dark brown
SnS
Pale brown
MnCO3
Light pink
Reddish pink
Red
Yellow
HgI2 , Pb 3O4
chromates
(ii)
Flame test :
Characteristic flame colour : Certain metals and their salts impart specific colours to Bunsen burner
flame.
(a) Pb imparts pale greenish colour to the flame.
(b) Cu and Cu salts impart blue or green colour to the flame.
(c) Ba and its salts impart apple green colour to the flame.
(d) Ca imparts brick red colour to the flame.
(iii)
241
(iv)
Cu
Green
Fe
Brown in cold
Ni
(2)
Acid Radical
Confirmatory test
Gas turns lime water milky but milkyness disappears on
passing gas inexcess,
(carbonate)
Brown fumes
(Nitrite)
(colourless);
(sulphide)
;
(brown)
Acid Radical
Confiramatory Test
Add MnO2 in the same test tube and heat-pale green Cl 2 gas
S.E.+ HNO 3 + AgNO3 solution white ppt. soluble in aq. NH 3
Chromyl chloride test
Add Mn2 O and heat yellowish brown Br 2 gas
S.E.+ HNO 3 + AgNO3 solution pale yellow ppt. partially
soluble aq. NH 3
(vi) Layer test
(vii) S.E.+ HNO 3 + AgNO3 yellow ppt. insoluble in aq. NH 3
(viii) Layer test
(i)
(chloride)
(ii)
(iii)
Br (bromide) (iv)
(v)
Cl -
I-
(iodide)
NO -3
(nitrate)
242
Reactions
Chloride :
(i)
HCl + NH 3 NH 4 Cl
( white fumes)
D
4 HCl + MnO2
MnCl2 + Cl 2 + 2H 2O
(ii)
(iii)
Pass these vapours into NaOH, when yellow Na2CrO4 solution is formed. On adding
CH 3COOH and (CH 3COO)2 Pb, yellow ppt. of lead chromate (PbCrO4 ) is formed.
Bromide :
(CrO2Cl 2 ).
(iv)
D
KBr + conc. H 2 SO4
KHSO4 + H
(v)
D
; 4 HBr + MnO2
Br2 + 2H 2 O + MnBr2
(vi)
shake
Layer Test : S.E. + Cl 2 water + CHCl 3
yellowish orange colour in layer or can be taken
instead of CHCl 3 );
2 NaBr + Cl 2 2 NaCl +
Br2
orange yellow
(soluble in CHCl 3 )
D
KI + conc. H 2 SO4
KHSO4 + HI
2HI + H 2 SO4
I 2 + 2H 2 O + SO 2
Nitrate :
NaNO 3 + H 2 SO4 NaHSO4 + HNO3
4 HNO3 4 NO 2 + O 2 2H 2 O
brown fumes
Cu + 4 HNO3
Cu ( NO3 ) 2 + 2 NO 2 + 2H 2 O
(viii) Ring test : To water extract (all NO 3- are water soluble) add freshly prepared FeSO4 solution and
then conc. H 2 SO4 carefully by the side of the test- tube. A dark brown ring of [Fe (H 2 O)5 NO] 2+ SO42at the interface between the two liquids is formed.
2 NaNO 3 + H 2 SO4 2 NaHSO4 + 2HNO3
243
Sulphate : S.E. add dil. (to decompose CO32- until reaction ceases). Add BaCl 2 solution. White ppt.
insoluble in conc. HNO 3 ,
(ii)
Borate : lgnite the mixture containing borate, conc. H 2 SO4 . And ethanol in a china-dish with a
burning splinter green edged flame of ethyl borate.
2 Na3 BO3 + 3 H 2SO4 2H 3 BO3 + 3 Na2SO4
(conc.)
D
H 3 BO3 + 3C 2 H 5 OH
(C 2 H 5 O) 3 B + 3 H 2 O
ethanol
(iii)
In presence of Cu 2+ , perform this test in a test tube since salts are not volatile.
S.E. + HNO3 + ammonium molybdate solution. Heat, yellow crystalline ppt. confirms
D
Na3 PO4 + 12( NH 4 )2 MoO4 + 24 HNO3
(iv)
Arsenic also gives this test. Hence presence of phosphate should also be checked after group II.
Fluoride : Sand +salt (F ) + conc. H2SO4; heat and bring a water wetted rod in contact with
vapours at the mouth of the test tube. A white deposit on the rod shows the presence to F .
D
NaF + H 2 SO 4
NaHSO 4 + HF
D
SiO2 + 4 HF
SiF4 + 2H 2 O
3SiF4 4 H 2 O
2H 2 SiF6 + H 4 SiO4
white
(3)
Group
I
II
Basic radicals
Ag + , Hg 22+ (I), Pb 2+
Cu 2+ , Cd 2+ , Pb 2 + ,
Hg
2+
(II), Bi 3+ , As 3+,
Sb3 + , Sn 2+
Group
reagent
dil HCl
Ppt. as
Explanation
Chloride
gas in
presence of
dil. HCl
H 2S
Sulphides
(CuS, As 2 S3 etc.)
III
Al 3+ , Cr 3 + , Fe 3+
NH 4 OH in
presence of
Hydroxide,
etc.
Al(OH) 3
NH 4 Cl
IV
Zn 2+ , Ni 2 + , Mn 2+ , Co 2+
in
H 2S
ammonical
medium
NH 4+
ion)
NH 4 OH
Ca 2 + , Ba 2+ , Sr 2+
( NH 4 )2 CO 3 +
NH 4 Cl
Carbonates ( CaCO 3
etc.)
244
VI
Mg 2 + , ( Na + , K + also
included)
0
NH 4+
NH 4 OH
White ppt.
+ Na 2 HPO 4 (MgHPO 4 )
Group
V
VI
Basic radicals
Group
reagent
Ppt. as
Explanation
Ca 2 + , Ba 2+ , Sr 2+
( NH 4 )2 CO 3 +
NH 4 Cl
Carbonates ( CaCO 3
etc.)
Mg 2 + , ( Na + , K + also
included)
0
(Zero)
NH 4 OH
White ppt.
+ Na 2 HPO 4 (MgHPO 4 )
NH 4+
Pb2+ (lead)
(i)
PbCl 2 is soluble in hot water and on cooling white crystals are again formed.
(ii)
The solution of PbCl 2 gives a yellow precipitate with potassium chromate solution which is insoluble
in acetic acid but soluble in sodium hydroxide.
PbCl 2 + K 2 CrO 4 PbCrO 4 + 2KCl
yellow ppt.
(iii)
The solution of PbCl 2 forms a yellow precipitate with potassium iodide solution.
PbCl 2 + 2KI PbI 2 + 2KCl
Yellow ppt.
(iv)
Group II : When hydrogen sulphide is passed in acidified solution, the radicals of second group are
precipitated as sulphides. The precipitate is treated with yellow ammonium sulphide. The sulphides of IIB
are first oxidised to higher sulphides which then dissolve to form thio-compounds.
Ag 2 S3 + 2( NH 4 ) 2 S 2 2( NH 4 ) 2 S + As 2 S5
Sb 2 S3 + 2( NH 4 ) 2 S 2 2( NH 4 ) 2 S + Sb 2 S5
SnS + ( NH 4 ) 2 S 2 ( NH 4 ) 2 S + SnS2
245
As 2S5 + 3( NH 4 )S 2( NH 4 )3 AsS4
Ammonium
thioarsenate
Sb2 S5 + 3( NH 4 )2 S 2( NH 4 )2 SbS4
Ammonium
thioantimonate
SnS2 + ( NH 4 )2 S ( NH 4 )2 SnS3
Ammonium
thiostannate
Pb2+ (lead)
In case the sulphide dissolves in dilute HNO3 , a small part of the solution is taken. Dilute H 2 SO4 is added.
If lead is present, a white precipitate of lead sulphate appears, Pb( NO3 )2 + H 2 SO4 PbSO4 + 2HNO3
(White ppt.)
In absence of lead, the remaining solution is made alkaline by the addition of excess of NH 4 OH. Bismuth
forms a white precipitat of Bi(OH )3 , copper forms a deep blue coloured solution while cadmium forms a
colourless soluble complex,
Bi( NO3 )3 + 3 NH 4 OH
Bi(OH )3 + 3 NH 4 NO3
White ppt.
Cu( NO3 )2 + 4 NH 4 OH [Cu( NH 3 )4 ] ( NO3 )2 + 4 H 2O;
Tetrammine cupric nitrate
(deep blue solution)
Cd( NO3 )2 + 4 NH 4 OH
[Cd ( NH 3 )4 ]( NO3 )2 + 4 H 2 O
Tetrammine cadmium nitrate
(colourless solution)
Cu2+ (copper) :
Blue coloured solution is acidified with acetic acid. When potassium ferrocyanide is added a chocolate
coloured precipitate is formed,
Cu( NH 3 )4 ( NO3 )2 + 4 CH 3 COOH
Cu( NO3 )2 + 4 CH 4 COONH 4
246
Group III : Hydroxides are precipitated on addition of excess of ammonium hydroxide in presence of
ammonium chloride.
AlCl3 + 3 NH 4 OH Al(OH )3 + 3 NH 4 Cl
Gelatinous ppt.
CrCl 3 + 3 NH 4 OH
Cr(OH )3 + 3 NH 4 Cl
Green ppt.
FeCl 3 + 3 NH 4 OH
Fe(OH )3 + 3 NH 4 Cl
Brownish red ppt.
Fe3+ (iron) : The brownish red precipitate dissolves in dilute HCl. The solution is divided into two parts.
Part I :
K 4 [Fe(CN )6 ]
Part II :
Addition of potassium thiocyanate solution gives a blood red colouration.
FeCl 3 + 3 KCNS Fe(CNS)3 + 3 KCl
Blood red colour
Al (aluminium) :
3+
The solution is boiled with ammonium chloride when Al(OH )3 is again formed.
NaAlO2 + NH 4 Cl + H 2 O
Al(OH )3 + NaCl + NH 3
Group IV : On passing H 2 S through the filtrate of the third group, sulphides of fourth group are precipitated.
NiS and CoS are black and insoluble in concentrated HCl while MnS (buff coloured), ZnS (colourless) are
soluble in conc. HCl.
Zn2+ (zinc) : The sulphide dissolves in HCl. ZnS + 2HCl ZnCl 2 + H 2 S
When the solution is treated with NaOH, first a white precipitate appears which dissolves in excess of NaOH
ZnCl 2 + 2 NaOH
Zn(OH )2 + 2 NaCl
White ppt.
(Soluble)
White ppt.
On heating the solution with NaOH and Br2 -water, manganese dissolve gets precipitated.
MnCl 2 + 2 NaOH
Mn(OH )2 + 2 NaCl
Mn(OH )2 + O
MnO2 H 2O
The precipitate is treated with excess of nitric acid and PbO2 or Pb3O4 (red lead). The contents are
heated. The formation of permanganic acid imparts pink colour to the supernatant liquid.
2MnO2 + 4 HNO3 2Mn( NO3 )2 +2H 2O + O2
2Mn( NO3 )2 + 5 Pb3 O4 + 26 HNO3
2HMnO4 + 15 Pb (NO3 )2 + 12 H 2 O
Permanganic acid (pink)
247
The solution is evaporated to dryness and residue extracted with dilute HCl. It is divided into three parts.
Part I : Add NH 4 OH (excess) and dimethyl glyoxime. A rosy red precipitate appears, if nickel is present,
CH 3 - C = NOH
NiCl 2 + 2
|
+ 2 NH 4 OH
CH 3 - C = NOH
OH
|
CH 3 - C = N
|
O
Ni
CH 3 - C = N
N = C - CH 3
|
+ 2 NH 4 Cl + 2H 2 O
N = C - CH 3
OH
Part II : Add CH 3COOH in excess and KNO2 . The appearance of yellow precipite confirms the presence
of cobalt.
KNO2 + CH 3 COOH CH 3 COOK + HNO2
CoCl 2 + 2KNO2 Co( NO2 )2 + 2KCl
Co( NO2 )2 + 2HNO2 Co( NO2 )3 + NO + H 2O
Co( NO2 )3 + 3 KNO2 K 3 [Co( NO2 )6 ]
Part III : Solution containing either nickel or cobalt is treated with NaHCO3 and bromine water. Appearance
of apple green colour is observed, the solution is heated when black precipited is formed, which shows the
presence of nickel, CoCl 2 + 2 NaHCO3 Co(HCO3 )2 + 2 NaCl
Co(HCO3 )2 + 4 NaHCO3 Na4 Co(CO3 )3 + 3 H 2O + 3CO2
Br2 + H 2 O 2HBr + O
NiCl 2 + 2 NaHCO3
NiCO3 + 2 NaCl + H 2O + CO2
2 NiCO3 + [O] Ni2 O3 + 2CO2
(Black)
248
M.C.Q.
1.
In borax bead test, which of the following compound is formed [CBSE PMT 2002]
(a) Meta borate
2.
(b) CuI
(c) NaCl
(d) MgCl2
(b) Strontium
(c) Calcium
(d) Magnesium
(b) Ni 2+
(c) Co 2+
(d) Mn 2+
(b) SO3
(c) NO
(d) NO2
Which one of the following salt give green coloured flame when the salt is tested by Pt wire
(a) Barium salt
8.
(d) Manganese
When concentrated H2SO4 is added to dry KNO3, brown fumes evolve. These fumes are
[CPMT 1988; IIT 1987]
(a) SO2
7.
(c) Lead
Which gives violet coloured bead in borax bead test [BHU 1988; MP PET 1997]
(a) Fe2+
6.
(b) Nickel
The alkaline earth metal that imparts apple green colour to the bunsen flame when introduced in
it in the form of its chloride is [EAMCET 1979]
(a) Barium
5.
4.
The metal that does not give the borax-bead test is [MP PMT 1999]
(a) Chromium
3.
(c) Borate
Sodium sulphite on heating with dilute HCl liberates a gas which [NCERT 1972]
(a) Turns lead acetate paper black
(b) Turns acidified potassium dichromate paper green
(c) Burns with a blue flame
(d) Smells like vinegar
9.
10.
(b) BaCl2
(c) pbCl2
(d) Cu(NO3)2
Blue borax bead is obtained with [MADT Bihar 1982; MP PET 1995]
(a) Zn
13.
Two gases when mixed give white dense fumes, the gases are
(a) NH3 and SO2
12.
Which of the following salt gives white precipitate with solution and dil. solution and gives green
flame test
(a) CuCl2
11.
(b) Cobalt
(c) Chromium
(d) Fe
Which of the following imparts green colour to the burner flame [DCE 2004]
(a) B(OMe)3
(b) Na(OMe)
(c) Al(OPr)3
250
(d) Sn(OH)2
14.
15.
16.
17.
18.
19.
20.
21.
22.
23.
24.
25.
(b) PH3
(c) SO2
MnO2 and H2SO4 added to NaCl, the greenish yellow gas liberated is [Orissa JEE 2005]
(a) Cl2
(b) NH3
(c) N2
(d) H2
Which of the following statement(s) is(are) correct when a mixture of NaCl and K2Cr2O7 is
gently warmed with conc H2SO4. [IIT 1998; CPMT 1988; AMU 1984; MP PMT 2002]
(a) A deep red vapour is evolved
(b) The vapour when passed into NaOH solution gives a yellow solution of Na2Cr2O7
(c) Chlorine gas is evolved
(d) Chromyl chloride is formed
Which of the following combines with Fe (II) ions to form a brown complex [AIIMS 1982, 87;
AFMC 1988; CBSE PMT 2000; Pb. PMT 2000; MP PET 2000, 01]
(a) N2O
(b) NO
(c) N2O3
(d) N2O5
Which of the following will not produce a precipitate with AgNO3 solution [MP PMT 1990]
(a) F
(b) Br
(c) CO32
(d) PO43
Which of the following gives black precipitate when H2S gas is passed through its solution
[CPMT 1974]
(a) Acidic AgNO3
(b) Mg(NO3)2
(c) Ammonical BaCl2 (d) Copper nitrate
A salt gives violet vapours when treated with conc. H2SO4. It contains [DPMT 1981; CPMT
1971]
(a) Cl
(b) I
(c) Br
(d) NO3
When water is added to a salt solution containing chloroform, chloroform layer turns violet. Salt
contains [CPMT 1982]
(a) Cl
(b) I
(c) NO3
(d) S2
Phosphate radical with ammonium molybdate gives precipitate of which colour
(a) Violet
(b) Pink
(c) Canary yellow
(d) Green
Which compound is soluble in NH4OH [AFMC 1987]
(a) PbCl2
(b) PbSO4
(c) AgCl
(d) CaCO3
Nitrates of all the metals are [DPMT 1983, 89]
(a) Coloured
(b) Unstable
(c) Soluble in water
(d) Insoluble in water
Nitrate is confirmed by ring test. The brown colour of the ring is due to the formation of
[EAMCET 1979; AFMC 1981, 88, 90; RPET 1999; MP PMT 2000; MP PET 2002; CPMT 2004]
26.
27.
(a) Cl
(b) Br
(c) I
(d) NO3
When CO2 is passed into lime water it turns milky. When excess of CO2 is passed, milkyness
disappears because
(a) Reaction is reversed
(b) Water soluble Ca(HCO3)2 is formed
(c) Vaporisable calcium derivative is formed (d) None of these
251
28.
29.
A mixture when heated with conc. H2SO4 with MnO2 brown fumes are formed due to
(a) Br
(b) NO3
(c) Cl
(d) I
In the test of sulphate radical, the white precipitate of sulphate is soluble in
(a) Conc. HCl
(b) Conc. H2SO4
(c) Conc. HNO3
(d) None of these
30.
31.
(a) BaSO4
(b) NaOH
(c) Pb(NO3)2
(d) KOH
........ is formed when potassium iodide is heated with conc. H2SO4 [CPMT 1971]
(a) HI
32.
33.
35.
(c) HIO3
(d) KIO3
Chromyl chloride test is performed for the confirmation of the presence of the following in a
mixture [CPMT 1990; KCET 1992; RPET 1999]
(a) Sulphate
(b) Chromium
(c) Chloride
(d) Chromium and chloride
A solution of a salt in dilute sulphuric acid imparts deep blue colour with starch iodine solution
it confirms the presence of which of the following [MP PET 2003; NCERT 1974; CPMT 1977]
(a) NO2
34.
(b) I2
(b) I
(c) NO3
(b) S2
(c) NO3
36.
The gas which is absorbed by ferrous sulphate solution giving blackish brown colour is
[AMU 1999]
(a) NO
(b) CO
(c) N2
(d) NH2
37.
Which one of the following anions is not easily removed from aqueous solutions by precipitation
[IIT 1995]
38.
(a) Cl
(b) NO3
(c) CO32
Na2CO3 cannot be used to identify [BVP 2004]
(a) CO32
(b) SO32
(c) S2
(d) SO42
(d) SO42
39.
The number of hydroxide ions, produced by one molecule of sodium carbonate (Na2CO3) on
hydrolysis is [Pb. CET 2002]
(a) 2
(b) 1
(c) 3
(d) 4
40.
(a) K2S
(d) MnO2
(b) S
(c) K2SO3
41.
Which of the following doesnt give a ppt. with silver nitrate solution. [J & K 2005]
(a) Ethyl bromide
(b) Sodium bromide (c)Calcium chloride
(d) Sodium chloride
42.
43.
(a) SnS
(b) AS2S3
(c) Sb2S3
(d) CdS
When acetic acid and K4[Fe(CN)6] is added to a copper salt, a chocolate precipitate is obtained
of the compound
(a) Copper cyanide
44.
45.
46.
47.
48.
49.
A precipitate of the following would be obtained when HCl is added to a solution of stannous
sulphide (SnS) in yellow ammonium sulphide [CPMT 1977; NCERT 1974]
(a) SnS
(b) SnS2
(c) Sn2S3
(d) (NH4)2 SnS3
The compound insoluble in acetic acid is [CPMT 1989]
(a) Calcium oxide
(b) Calcium carbonate (c) Calcium oxalate
(d) Calcium hydroxide
Which of the following give white precipitate when HCl is added to its aqueous solution
(a) Hg+
(b) Mg++
(c) Zn++
(d) Cd++
Reagent used in the qualitative analysis of IVth group is
(a) HCl
(b) H2S (alkaline)
(c) (NH4)2S
(d) None of these
Which of the following pairs would be expected to form precipitate when solution are mixed
[NCERT 1984]
(a) K+, SO42
(b) Na+, S2
(a) Ca2+
(d) Al3+, OH
Addition of solution of oxalate to an aqueous solution of mixture of Ba2+, Sr2+ yLku Ca2+ and will
precipitate [MP PMT 1985]
(c) Ba2+, Sr+2
50.
Distinguishing reagent between silver and lead salts is [MADT Bihar 1984]
(a) H2S gas
(b) Hot dilute HCl solution
(c) NH4Cl(S) + NH4OH(aq) (solid) + solution (d) NH4Cl(S) (solid) + (NH4)2 CO3(aq) solution
51.
The ion that cannot be precipitated by both HCl and H2S is [IIT 1982; CPMT 1989]
52.
53.
54.
55.
56.
57.
58.
(a) Pb2+
(b) Cu2+
(c) Ag+
(d) Sn2+
Pb(CH3COO)2 gives.colour with H2S [DPMT 2000]
(a) Orange
(b) Red
(c) Black
(d) White
2+
3+
Fe
ion can be distinguished by Fe ion by [DPMT 2000]
(a) NH4SCN
(b) AgNO3
(c) BaCl2
(d) None of these
Which of the following change the colour of the aqueous solution of FeCl3 [Roorkee Qualifying
1998]
(a) K4[Fe(CN)6]
(b) H2S
(c) NH4CNS
(d) KCNS
Which of the following mixture is chromic acid [Pb. PMT 2000]
(a) K2Cr2O7 and HCl
(b) K2SO4 conc. H2SO4
(c) K2Cr2O7 and conc. H2SO4
(d) H2SO4 and HCl
If Na+ ion and S2 ion is larger than Cl ion, which of the following will be least soluble in water
[AMU (Engg.) 1999]
(a) MgS
(b) NaCl
(c) Na2S
(d) MgCl2
Lead sulphate is soluble [MP PET 1999]
(a) In conc. nitric acid
(b) In conc. hydrochloric acid
(c) In a solution of ammonium acetate
(d) In water
When H2S gas is passed through the HCl containing aqueous solutions of CuCl2, HgCl2, BiCl3
and CoCl2, which does not precipitate out [MP PMT 2002]
(a) CuS
(b) HgS
(c) Bi2S3(d) CoS
253
59.
60.
61.
62.
63.
64.
65.
66.
67.
68.
69.
70.
71.
72.
73.
(a) CrO42
(b) PO43
(c) MnO4
(d) NH4+
254
74.
75.
76.
77.
78.
79.
80.
81.
82.
83.
84.
85.
(a) Hg2Cl2
(b) Hg2+
(c) Hg2I2
(d) HgI42
Which one of the following sulphides is only completely precipitated when the acidic solution is
made dilute [MP PET 2000]
(a) HgS
(b) PbS
(c) CdS
(d) CuS
A reagent used to test the presence of ion is [KCET 1998]
(a) H2S
(b) NH4CNS
(c) K4[Fe(CN)6]
(d) K3[Fe(CN)6]
The following four solutions are kept in separate beakers and copper metal is put in each of them.
Which solution will become blue after some time [MP PMT 2003]
(a) AgNO3 solution
(b) Zn(NO3)2 solution (c) Ba(NO3)2 solution (d) NaNO3 solution
In qualitative analysis, in order to detect second group basic radical, H2S gas is passed in the
presence of dilute HCl to [KCET 2004]
(a) Increase in dissociation of H2S
(b) Decrease the dissociation of salt solution
(c) Decrease the dissociation of H2S
(d) Increase the dissociation of salt solution
Sodium nitroprusside when added to an alkaline solution of sulphide ions produce a [AFMC 2005]
(a) Red colouration
(b) Blue colouration
(c) Purple colouration (d) Brown colouration
If 20 ml of 0.25 N strong acid and 30 ml of 0.2 N of strong base are mixed, then the resulting
solution is [KCET 2002]
(a) 0.25 N basic
(b) 0.2 N acidic
(c) 0.25 N acidic
(d) 0.2 N basic
10 ml of 10 M H2SO4 is mixed to 100 ml 1M NaOH solution. The resultant solution will be
[NCERT 1971]
86.
87.
88.
(a) Acidic
(b) Neutral
(c) Weakly alkaline
(d) Strongly alkaline
The equivalent weight of KMnO4 in alkaline medium will be [MP PMT 2001]
(a) 31.60
(b) 52.66
(c) 79.00
(d) 158.00
Phenolphthalein is most suitable indicator for the titration of
[MP PMT 2000]
(a) CH3COOH and NH4OH
(b) CH3COOH and NaOH
(c) HCl and NH4OH
(d) H2CO3 and NH4OH
20 ml of a N solution of KMnO4 just reacts with 20 ml of a solution of oxalic acid. The weight
of oxalic acid crystals in 1N of the solution is [JIPMER 1999]
(a) 31.5 g
(b) 126 g
(c) 63 g
(d) 6.3 g
255
ANSWERS KEY
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
a
c
a
d
d
d
a
b
a
b
c
b
a
b
a
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
a,b,d
b
d
a
b
b
c
c
c
b
a
b
a
d
c
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
b
c
a
c
b
a
b
a
a
b
a
b
b
b
c
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
256
a
b
d
d
b
b
c
a
a
c
a
a
d
b
c
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
c
c
b
d
b
a
a
a
a
d
b
a
d
c
b
76
77
78
79
80
81
82
83
84
85
86
87
88
b
b
d
c
d
a
c
c
d
a
d
d
c
NOTES
257
NOTES
258
NOTES
259
NOTES
260
NOTES
261
NOTES
262
NOTES
263
NOTES
264
NOTES
265
NOTES
266
NOTES
267
NOTES
268