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Chemistry MCQ BANK
Chemistry MCQ BANK
Chemistry MCQ BANK
BY
ABDUL MANAN
Facebook group Expert MDCAT
FUNDAMENTAL CONCEPTS
The number of atoms present in a molecule of a substance is called ________.
(A) Atomicity ®
(B) Volume
(C) Density
(D) Mass
a. 27
b. 21 ®
c. 8
d. 5
There are three isotopes of Si. They have mass number of 28, 29 and 30. The average atomic mass of
silicon is 28.086 amu. What does this say about % abundance of isotopes?
Average atomic mass is closer to the mass of Si-28 isotope so it will have greater % abundance
An element X has two isotopes X-35 and X-37 with average atomic mass 35.5 amu. Relative abundance
of both isotopes:
a. 50%, 50%
b. 25%, 75%
c. 75%, 25% ®
d. 40%, 60%
Average atomic mass is closer to mass of X-35. So X-35 will have greater % abundance. So the possible
answer from given options is option C
An element has two isotopes A-63 and A-64 with average atomic mass 63.5 amu. Relative abundance of
lighter isotope is :
a. 50%
b. 40%
c. 25%
d. 75%
relative atomic mass = 63.5. It is equally differ from 63 and 64 i.e 0.5 . So abundance of both isotopes
will be equal
What will be the Percentage abundance of each isotope of copper having mass numbers of 63 and 65
based on average atomic mass of 63.55amu?
a. 72.5% , 27.5%
b. 27.5%, 72.5%
c. 50%, 50%
d. 60%, 40%
As average atomic mass is closer to Cu-63 so it will have greater % abundance. From given options,
eliminate options B and C. Now to whether it is option A or option D, use equation: (x)(63) + (1-
x)(65) = 63.55 ----> 63x + 65 - 65x = 63.55 -2x = 63.55 - 65
----> -2x = - 1.45 ---> x = 0.725 × 100 = 72.5%(Cu-63) 100%-72.5% =
27.5%(Cu-65)
The natural isotopes of boron are B-10 and B-11. If boron has atomic mass is 10.81 amu, what will be
the % abundance of each isotope?
a. 50%, 50%
a. 20%, 80% ®
c. 80%, 20
d. 75%, 25%
As average atomic mass is closer to B-11 so it will have greater % abundance. From given options, only
option B have greater % of B-11 so it is the right answer. No need to calculate
Suppose an element has 3 isotopes X-18, X-19, X-20. Their relative abundances are 84%, 6% and 10%
respectively. What will be the supposed value of relative atomic mass of element?
a. 18.000
b. 19.000
c. 20.000
d. 13.000
No need to solve. Just see which isotope has greater percentage abundance. Relative atomic mass is
always closer to the isotope of greater abundance. Here X-18 has very high % abundance. So the
supposed value of relative atomic mass will be 18.000.
In chemical scale, the relative mass of isotopic mixture of oxygen atoms (O16, O17, O18) is assumed to
be equal to :
a. 16.002
b. 16.00 ®
c. 17.00
d. 11.00
% composition of O16 is much greater than O17 and O18 thats why mass of O16 is taken as relative
mass of isotopic mixture. % composition of O16 = 90% and % composition of O17 = 7%. % composition
of O18= 3%
Boron has two stable isotopes 10-B(19%) and 11-B(81%). The atomic mass that should appear for boron
in periodic table :
a. 10.8 ®
b. 10.2
c. 10.0
d. 11.2
No need to solve. Just see which isotope has greater abundance. Relative atomic mass is always closer
to that isotope which has greater abundance. B-11 has greater abundance. Its mean atomic mass of
Boron will be closer to the 11. From given options, option A is closer to B-11 so it is the right answer.
Atomic mass can never be greater than the mass of its isotope. You can calculate it by using formula :
Atomic mass = 10×19 + 11×81/100 = 1081/100
The relative atomic mass of chlorine is 35.5 . What is the mass of 2 mole of chlorine gas?
a. 142g ®
b. 35.5g
c. 71g
d. 18.75g
A) Ca
B) Pd
C) Cd ®
D) Sn
a. 9
b. 16 ®
c. 6
d. 18
a. F
b. Cl ®
c. I
d. Au
Out of 280 isotopes which occur in nature, tge radioactive iostopes are:
a. 116
b. 126
c. 30
d. 40 ®
Isotopes are sister atoms of same element with similar chemical properties but different :
a. Atomic number
b. Atomic volume
c. Atomic weight
d. Atomic structure
Isotopes have different atomic mass, number of neutron, radioactive properties, physical properties,
half life, stability
A) Magnesium chlorate
B) magnesium perchlorate
solution of
A) Mg(ClO4)2 ®
B) 50% KOH
D) Mg(ClO3)2
_____ of a compound is the chemical formula indicating the relative number of atoms in the
simplest ratio.
The empirical formula of an acid is CH2O2, the probable molecular formula of acid may be
(A) CH2O
(B) CH2O2 ®
(C) C2H4O2
(D) C3H6O4
By knowing Emperical formula, what other information is also needed to calculate molecular formula of
a compound?
a. % composition
b. Density of a compound
c. Volume occupied
A compound has Emperical formula C3H3O and its molecular mass is 110. Its molecular formula :
a. C3H3O
b. C6H6O2
c. C9O3H9
d. C3H6O3
(A) 70 g C6H6
(B) 72 g C6H6
(C) 10 g C6H6
(D) 78 g C6H6
Molecular formula of benzene is C6H6 ∴
Molecular mass = sum of atomic weight of all the atoms Molecular mass
= 12 × 6 + 6 × 1= 72 + 6 = 78 According to
Avogadro’s number, The gram molecules of benzene is equal to 78g of C6H6
The molecular mass of an organic compound is 78. Its empirical formula is CH. The molecular formula is
(A) C2H4
(B) C2H2
(C) C6H6
(D) C4H4
Two elements X (Atomic mass 75) and Y (Atomic mass 16) combine to give a compound having 75.8% X.
The formula of the compound is
(A) XY
(B) XY2 ®
(C) X2Y2
(D) X2Y3
A compound made of two elements A and B are found to contain 25% A (Atomic mass 12.5) and 75% B
(Atomic mass 37.5). The simplest formula of the compound is
(A) AB ®
(B) AB2
(C) AB3
(D) A3B
Number of moles = % composition/atomic mass
25/12.5 = 2 moles of A and 75/37.5 = 2 moles of B Simplest
ratio 1 : 1
Which one of the following is the molecular formula of hydrocarbon which contains 80% by mass of
carbon and 20% by mass of hydrogen?
a. CH4
b. C2H6
c. C3H6
d. C2H4
(A) C2H2O2
(B) C2H2O
(C) CH2O2
(D) CH2O
A) 2.24 dm³ ®
B) 22.4 dm³
C) 1.12 dm³
D) 112 cm³
a. 0.16g
b. 0.8g
c. 0.08g ®
d. 1.6g
a. C2H2 ®
b. CO
c. O2
d. CH4
Under similar conditions, oxygen and nitrogen are taken in the same mass. The ratio of their volumes
will be_______.
(A) 7 : 8 ®
(B) 3 : 5
(C) 6 : 5
(D) 9 : 2
What will be the ratio of volumes of equal masses of O2, H2, CH4 kept in the same container under
same condition?
A. 2:16:2
B. 1:16:2
C. 2:16:1
D. 1:2:1
A) 1 : 1
B) 1 : 2
C) 1 : 8
D) 2 : 1 ®
Which of the following reactions has the ratio of volumes of reacting gases and the product as 1:2:2?
The volume of oxygen required for complete combustion of 0.25 cm3 of CH4 at S.T.P is
(A) 0.25 cm3
(D) 1 cm3
How many litres of ammonia will be formed when 2 L of N2 and 2 L of H2 are allowed to react?
(A) 0.665
(B) 1.0
(C) 4.00
(D) 1.33 ®
a. NA
b. NA/2 ®
c. 2 × NA
d. NA/4
a. NA
b. NA/2 ®
c. 2 × NA
d. NA/4
2g of H2 = NA molecules
1g of H2 = NA/2 molecules
b. 18g ®
c. 1g
(A) 8g m
(B) 16 g
(C) 24 g
(D) 48 g
1 mole of ozone(O3) = 48 g
0.5 mole of ozone(O3) = 0.5 × 48/1 = 24g
(A) 8g
(B) 32g ®
(C) 16g
Oxygen exists in molecular form. 16 would be the right answer if question was one mole of atom of
oxygen weigh
The number of atoms present in one mole of an element is equal toAvogadro number. Which of the
following element contains the greatest number of atoms?
(a) 4 g He
(b) 46 g Na
(c) 0.40 g Ca
(d) 12 g He ®
(A) 1 g CO2
(B) 1 g N2
(C) 1 g H2 ®
(D) 1 g CH4
(A) 50
(C) 25
(D) 100
Number of He atoms = number of amu/atomic mass = 100/4 = 25
(A) 1 g
(B) 0.5 g
a. 2.4 NA
b. 4.2 NA
c. 1.6 NA
d. 3.2 NA
N-³ has 5+3=8 valence electrons 14g N-³ = 8 NA valence electrons 4.2g N-³
= 8NA×4.2/14 = 2.4 NA
What mass of CaO will be obtained by heating 3 mole of CaCO3 [Atomic mass of Ca = 40] ?
(A) 150 g
(B) 168 g
(C) 16.8 g
(D) 15 g
(A) 1032.2 g
(B) 11332 g
(C) 1133.3 g
(D) 8692.6 g
N2 + 3H2 ⎯→ 2NH3
(28g) (6g) (34 g)
6 gms of H2 produces 34 gms NH3
200 gms of H2 produces 34×200/6= 1133.3 g
Amount of Zn required to produce 224ml of H2 at STP on treatment with dilute H2SO4 will be :
a. 6.5g
b. 0.65g
c. 65g
d. 0.065g
a. One mole of H2
b. 0.5 mole of H2 ®
c. 2/3 mole of O2
a. 6.02 × 10²³
b. 18 × 6.02 × 10²³
d. 18/24 × 10²³
In a sample of glucose, there are 3.6 × 10²⁴ atoms of carbon are present. Mass of glucose sample :
a. 180g ®
b. 360g
c. 3600g
d. 342g
a. 9g ®
b. 36g
c. 16g
d. 72g
2 H2 + O2 --------> 2 H2O
H2 : H2O O2 : H2O
4g : 36g 32g : 36g
8g : 72g 8g : 9g
10g of CaCO3 is heated to produce CaO and CO2. The amount of CO2 produced is :
a. 44g
b. 4.4g
c. 22g
d. 2.2g
27g Al will react completely with how much mass of O2 to produce Al2O3?
a. 8g
b. 32g
c. 16g
d. 24g
a. 28 moles ®
b. 18 moles
c. 26 moles
d. 20 moles
O has 8 protons, 8 electrons and 8 neutrons. Hydrogen has 1 electron and 1 proton. 2 hydrogens will
have 2 protons and 2 electrons. So total number of moles of fundamental particles are 28.
The molecular mass of hydrogen peroxide is 34. What is the unit of molecular mass?
(A) g
(B) mol
(C) g mol−1 ®
10 dm³ of N2 gas and 10 dm³ of gas X at the same temperature contain the same number of molecules.
The gas X is
(A) CO
(B) CO2
(C) H2
(D) NO
a. 100
b. 200
c. 400
d. 355
(A) 33
(B) 22
(C) 44 ®
(D) 11
_____ reactant is the reactant that reacts completely but limits further progress of the
reaction.
(A) Oxidizing
(B) Reducing
(C) Limiting ®
(D) Excess
_____ reactant is the reactant which is taken in excess than the limiting reactant.
(A) Oxidizing
(B) Reducing
(C) Limiting
(D) Excess ®
Carbon react with chlorine to form CCl4. 36g of carbon was mixed with 142g of Cl2 . The remaining mass
of excess reactant for completion of reaction :
a. 0g
b. 24g
c. 12g
d. 6g
C + 2Cl2 ------> CCl4 According to the reaction, 12g of carbon is reacting with 142g of Cl2 to produce
154g of CCl4 while 36g of carbon was taken. Its mean carbon is in excess and Cl is a limiting reactant.
Amount of C left = taken - used = 36-12 = 24g
8g oxygen reacts with 8g hydrogen to produce water. Which of the following is limiting reactant?
a. Oxygen
b. Hydrogen
d. Oxygen or hydrogen
2 H2 + O2 ----------> 2 H2O
2 mol + 1 mol ----------> 2 mol
4g + 32g ----------> 36g
4g of hydrogen produce 36g water so 8g hydrogen will produce 72g water
32g oxygen produce 36g water so 8g oxygen will produce 9g water Limiting
reactant produce least amount of product so Oxygen is limiting reactant
a. 4.5
b. 5.6
c. 8.09 ®
d. 6.6
C6H6 + HNO3 -----> C6H5NO2 + H2O
78g -----> 123g
5g -----> 123/78 × 5 = 7.88g
a. molality
A) Molality
B) Molarity ®
C) Mole fraction
D) W/W %
a. 1
b. 55.5 ®
c. 1000
d. 18
a. 2M
b. 1M
c. 0.5M
d. 0.25M
a. 0.5
b. 0.1
c. 1 ®
d. 2
Molarity = moles/Volume
How many grams of HCl will be present in 150ml of its 0.52 M solution :
a. 2.84 g
b. 5.70 g
c. 8.50 g
d. 3.65 g
a. 250ml solvent
b. 250g solvent
c. 250ml solution ®
d. 1000ml solvent
A) 1 dm3
B) 1.8 dm3 ®
C) 200 cm3
D) 900 cm3
a. 90g
b. 180g
c. 100g
d. 45g
The density (in g mL-¹) of a 3.60 M sulphuric acid solution that is 29% H2SO4 (Molar mass = 98 g mol–1)
by mass will be:
a. 1.45
b. 1.64
c. 1.88
d. 1.22 ®
The relation between Molarity, M and mass percent (%) is given by: M = (% x 10 x d) / MW
Two glucose solutions are mixed. One has volume of 480mL and conc. of 1.50M and second solution has
volume of 520mL and conc. of 1.20M. The molarity of final solution:
a. 1.20M
b. 1.50M
c. 2.70M
d. 1.34M ®
If 500 mL of a 5M solution is diluted to 1500 mL, what will be themolarity of the solution obtained?
(a) 1.5 M
(b) 1.66 M ®
(c) 0.017 M
(d) 1.59 M
If the concentration of glucose (C6 H12 O6) in blood is 0.9 g L-¹, what willbe the molarity of glucose in
blood?
(a) 5 M
(b) 50 M
(c) 0.005 M ®
(d) 0.5 M
In the given question, 0.9 g L-¹ means that 1000 mL (or 1L) solution contains 0.9 g of glucose No. of
moles = 0.9g/180g = 0.005 moles 1L
solution has 0.005 moles of glucose or Molarity is 0.005M
a. Temperature
b. Volume
c. Pressure
d. All of these ®
2 moles of N2 , 3 moles of H2 and 5 moles of O2 are present in a container, the mole fraction of oxygen
gas is :
a. 0.5
b. 1.0
c. 0.25
d. 0.75
A solution contains three components x, y and z. Mole fraction of x and y are 0.3 and 0.4 respectively.
What is mole fraction of z component?
a. 0.1
b. 0.2
c. 0.3 ®
d. 0.4
a. 0.050
b. 1.100
c. 0.190
d. 0.086
molality of aqueous solution = 5.2 mol kg-¹ Therefore, the number of moles of methyl alcohol in 1 kg of
solvent (water) = 5.2 mol And the number of moles of solvent (water) = weight / molar mass =
1000g/18g mol-¹ = 55.55 mol Mole fraction
of methyl alcohol = nMeOH/nMeOH + nwater = 5.2 / 55.55 + 5.2 = 0.08559
a. 9
b. 0.03
c. 1.77
d. 0.017
(A) 40%
(B) 50%
(C) 20%
(D) 80%
(A) 46 %
(B) 85 %
(C) 18 %
(D) 28 %
(A) 45
(B) 30
(C) 19
(D) 25
(A) 40 ®
(B) 60
(C) 8
(D) 10
A) 40%
B) 48% ®
C) 12%
D) 165
STATES OF MATTER
A) Low temperature
B) Low pressure ®
C) High pressure
In general, gases are very poor conductors of electricity at normal atmospheric pressure as they are
deficient of free electrons to carry the current. But when subjected to lower pressure and higher voltage,
gases can conduct electricity. So the required conditions need to be artificially created in a laboratory in
order for the gas to become a conductor of electricity.
a. One Pascal
b. One mm of Hg ®
c. 76cm of Hg
d. One atm
If absolute temperature of gas is reduced to ½ and pressure is doubled, the volume of gas will
A) Remains unchanged
C) Reduce to 1/4th ®
D) Be doubled
A) Temperature of gas
C) Volume of gas
A) 5
B) 80
C) 125
D) 10
A) 30 dm³ ®
B) 3 dm³
C) 0.3 dm³
D) 1.5 dm³
A) It is a continuous process
B) It is a surface phenomena
C) It causes cooling
D) It is exothermic ®
a. 150cm³ ether ®
b. 50cm³ ethanol
c. 150cm³ water
d. 150cm³ ethanol
Vapour pressure of a substance depends upon temperature, strength of intermolecular forces, density
and size of molecules. It does not depend upon amount of liqued, volume of container and surface area
of liqued. Ethanol and water has H-bond and have greater boiling points so they have lesser vapour
pressure while ether has weaker forces and have greater vapour pressure
A) 55 mm Hg
B) 760 mm Hg ®
C) 355 mm Hg
D) 1489 mm Hg
With the increase of carbon atoms in class of organic compounds, which property decreases?
A) Viscosity
B) Density
C) Melting point
D) Vapour pressure ®
A) Molecular mass
B) Size of molecule
C) H-bond ®
Vapour pressure of a substance depends upon temperature, strength of intermolecular forces, density
and size of molecules. It does not depend upon amount of liqued, volume of container and surface area
of liqued.
a. Ethanol
b. Acetone
c. Acetic acid ®
d. Water
Vapour pressure of a substance depends upon temperature, strength of intermolecular forces, density
and size of molecules. It does not depend upon amount of liqued, volume of container and surface area
of liqued. Acetic acid has greater boiling point due to stronger intermolecular forces. Here acetone has
greatest vapour pressure because acetone(propanone) has dipole forces while remaining have H-
bonding
A) Water
B) Acetone
C) Ammonia ®
D) Ethyl alcohol
Water, Ammonia and ethyl alcohol has hydrogen bonding. While acetone(propanone) has dipole forces
but acetone has higher boiling point than ammonia. An exception because ammonia has very weak
hydrogen bonding. Water > ethyl alcohol > acetone > ammonia
a. 150mmHg
b. 700mmHg
c. 760mmHg
d. 1489mmHg®
a. C2H6
b. C4H10
c. CH4
d. C6H14 ®
Greater the number of atoms in a molecule, greater is its polarizabiliy and hence stronger will be London
forces
Propanone(acetone) has dipole forces while propane has Vander Waal's forces
Hydrides of which one of the following group has relatively low boiling points?
A) IV-A ®
B) VI-A
C) V-A
D) VII-A
Intermolecular forces(s) responsible for the fact that CH4 has the lowest boiling point in the set " CH4,
SiH4, GeH4, SnH4" is/are
(a) molecule
(b) ion
(c) electron
(d) atom
Each point in a lattice is known as lattice point which are either atom or molecule or ion which are
joined together by a straight line to bring out geometry of lattice in pure crystal constituents are
arranged in fixed stoichiometric ratio.Hence, existence of free electrons are not possible, it is possible on
in case of imperfection in solid.
Which is the example of crystalline solid
A) Glass
B) Rubber
C) Plastic
D) Quartz ®
a. Metallic crystal
b. Ionic crystal ®
c. Covalent crystal
d. Molecular crystal
c. Simple cube
d. Hexagonal
A) 3
B) 5
C) 4 ®
D) 6
b. 2
c. 4
d. 6 ®
In crystal of sodium chloride, a Cl- ion is present at corner of cube is shared between how many cubes?
a. 2
b. 4
c. 6
d. 8 ®
A) Graphite
B) Sugar
C) Tin
D) Diamond ®
a. Tetrahedral
b. Hexagonal ®
c. Tetragonal
d. Trigonal
a. 30 ®
b. 28
c. 32
d. 34
(A) 4
(C) 5
(B) 6 ®
(D) 7
Number of protons, electrons and neutrons in a nucleus of atomic number 11 and mass number 24 are
a. 11, 13, 0
b. 11, 0, 13 ®
c. 24, 0, 11
d. 0, 13, 11
(A) 10
(B) 4
(C) 1
(D) 2 ®
The number of electrons in the M shell of the element with atomic number 24 is
(A) 24
(B) 14
(C) 13 ®
(D) 8
K shell = 1s L shell = 2s, 2p M shell = 3s, 3p, 3d N shell = 4s, 4p, 4d, 4f
(A) 6
(B) 8 ®
(C) 10
(D) 4.
The atomic number of an element is 35. What is the total number of electrons present in all the p-
orbitals of the ground state atom of that element ?
(A) 6
(B) 11
(C) 17 ®
(D) 18
A element M has an atomic mass 19 and atomic number 9. Its ion is represented by
(A) M+
(B) M2+
(C) M–
(D) M2
Z=9, thus the ground state electron configuration is 1s², 2s², 2p5 . It needs one more electron to attain
stable electron configuration of Ne. Thus, its ion is M−.
(A) 4l - 2
(B) 4l + 2 ®
(C) 2l + 1
(D) 2n²
(A) 14 ®
(B) 10
(C) 8
(D) 4
Number of electrons in subshell = 2(2l+1)
The total number of electrons present in any main energy level can be calculated from
(A) (2l + 1)
(B) 2n²®
(C) (2n+1)
(D)n2
Which of the following particles would, on losing an electron, have a half-filled set of p-orbitals?
(A) �−
(B) �− ®
(C) N
(D) �+
E.C of �− = 1s², 2s², 2p⁴ So it on losing an electron would have half filled p-orbital
(A) 6
(B) 10
(C) 14 ®
(D) 18
(B) 7s
(C) 7p ®
(D) 7d
Three dimensional space around nucleus where probability of finding electrons is maximum is called :
a. Orbit
b. Orbital ®
c. Nodal plane
d. Shell
a) Mass number
b) Atomic number
c) Neutrons
d) Number of protons
An ion would have the same atomic number as its parent atom. Neutrons are found in the nucleus of
atom. They don't help in formation ions though. They are a constant for both atoms and ions.
Similarly,number of protons don't change during formation of ionsThe atoms differ with an ion in its
Mass number. since electrons have approximately zero mass an atom or an ion will have approximately
the same mass. Mass of an atom is determined by the protons and neutrons in the nucleus, which each
have a mass of 1 atomic mass unit (or 1 gram per mole as the mole is defined). Like I said the mass of an
electron is approximately zero, however in reality it is 0.00055 atomic mass units at rest. So, if we’re
being super nitpicky an ion with more electrons (so a negative ion) will weight slightly more than a
neutral ion, while a positive ion (less electrons) will weigh slightly less.
Which subshell has greater energy :
a. 1s
b. 2s
c. 2p
d. 3s ®
The total number of orbitals in a shell with principal quantum number ‘n’ is
(A) 2n
(B) 2n²
(C) n² ®
(D) n + 1.
In a set of degenerate orbitals the electrons distribute themselves to retain similar spins as far as
possible. This statement is attributed to
(A) spherical
(B) tetrahedral
(C) dumb-bell ®
(D) pyramidal
a. 0°
b. 90° ®
c. 180°
d. 45°
a. 2px
b. 2pz
c. 3px ®
In absence of magnetic field, orbitals of same subshell has same energy. So 2px and 2pz have same
energy while energy of 3px is greater. Greater the n+l value greater will be the energy
b. 2py
c. 2pz
In absence of magnetic field, all three 3 p-orbitals have same energy and are called degenerate orbitals
a. 2px
b. 3px
c. 4px ®
With the increase of principal quantum number of the shell, size of orbital increase
a. dxy
b. dyz
c. dxz
d. dz² ®
Out of 5 d-orbitals, only dz² has two lobes while others have 4 lobes
a. 2
b. 6
c. 14
a. Hydrogen ®
b. Helium
c. Oxygen
d. Nitrogen
a. 2 ®
b. 8
c. 14
d. 18
a. Alpha particle
b. Beta particle
d. Ionized helium
Mass of proton is :
a. 1.0073 amu ®
b. 1.0087 amu
c. 5.4 × 10⁴ amu
d. 1.5 × 10-¹° kg
a. Proton
b. Electron
c. Neutron ®
d. Meson
Proton is 1836 times heavier than electron while neutron is 1840 times heavier than electron.
a. 1.602 × 10*19 C
b. 1.602 × 10-19 C
c. 1.758 × 10-¹¹ C
d. 1.758 × 10¹¹ C ®
a. K+
b. Ca+²
c. Cl-
d. F- ®
F has tendency to gain electron to gain electron configuration of nearst noble gas Neon gas
Ar has 18 electrons. Thus, the species isoelectronic with it will also have 18 electrons. Some of its
isoelectronic species are K+ (19-1=18), Cl- (17+1=18), Ca+² (20-2=18), S-² (16+2=18)
(A) 1836
(B) 1840 ®
(C) 1700
(D) 3000
Which one of the following has the same number of electrons as an alpha particle?
(A) H
(B) H2
(C) �+ ®
(D)He
Which of the following formulae represents a particle with the composition 1 proton, 1 neutron and 2
electrons? (D represents deuterium)
(A) D
(B) �−
(C) �− ®
(D) He
Deutron has one proton, one electron and one neutron. �− is indicating gain of electron.
(A) 2 : 1 ®
(B) 1 : 2
(C) 1 : 1
(D) 1 : 4
(A) 1s°
(C) 1s² ®
(B) 1s¹
(D)1s², 2s¹
a. NF3
b. CH4
c. CCl4
d. PCl5 ®
PCl5, PF5, BCl3, SF6 do not follow octet rule and hence octet could not be made universal
a. 12
b. 14 ®
c. 16
d. 8
Ionization energy does not depend upon one of the following factor
A) atomic number
B) shielding effect
C) nuclear force
D) mass number ®
Which of the following electrons should have highest value of ionization energy (for same value of
principle quantum number)
a. s ®
b. p
c. d
d. f
s electrons are strongly bounded to nucleus so Large amount of energy is required for removal of
electron
a. Alkali metals ®
c. Halogens
d. Inert gases
Lower the no. of valence electrons lower is the value of ionization potential
a. Li ®
b. He
c. H
d. Fe
a. Metals ®
b. Non metals
c. Semi metals
d. Metalloids
a. Nobal gases ®
b. Transition elements
c. Platinum metal
a. B
b. K
c. Na
d. Kr ®
a. B
b. Li
c. Ne ® noble gas
d. F
a. He ®
b. H
c. N
d. B
the first ionization energy of beryllium is greater than that of boron because beryllium has a stable
complete electronic configuration (1s², 2s²) so it requires more energy to remove the first electron from
it. Electronic configuration of boron is 1s², 2s², 2p¹ Ionization energies of
III-A and VI-A show abnormal trend
Highest energy will be absorbed to eject out e- in configuration
a. Li ----> Li+
b. Cu ----> Cu+
c. Br ----> Br-
d. I ----> I-
In option c and d, energy is releasing(electron affinity). Cu has completely filled d orbital so highest
energy is absorbed during conversion. Moreover, alkali metals have very low ionization energy.
Ionization energy increases from left to right in period. Ionization energies of III-A [Al] and VI-A show
abnormal trend
a. 1
b. 2
c. 4 ®
d. 6
a. P ®
b. Si
c. Mg
d. Al
P belongs to group having nitrogen means P has Stable half filled configuration. Further Ionization
energy increases from left to right in period.
Which ionization potential in the following equations involve greatest amount of energy?
K on losing 1 electron gains electronic configuration of Argon(noble gas). Now Electron has to be
removed from stable configuration. C+² = Be . Now compare ionization energy of C+² with Noble gas
configuration (K+). In mcqs, whenever you see noble gas, mark that option without any hesitation.
Noble gases have very high ionization energies due to stable configuration.
a. 419 kj/mol ®
b. -349 kj/mol
c. 721 kj/mol
d. 1870 kj/mol
Lattice energy of KCl is :
a. 720 kj/mol
b. 690 kj/mol ®
c. 1265 kj/mol
d. 1768 kj/mol
a. Na
b. Mg ®
c. Al
d. K
Ionization energy increases from left to right in period. Ionization energies of III-A [Al] and VI-A show
abnormal trend.
First four ionization potential values of an element are 191, 578, 872 and 5962 kcal. The number of
valence electrons in element are:
a. 1
b. 2
c. 3 ®
d. 4
Larger gap between 3rd and 4th ionization energies. Since 4th I.E is very high. Thus electron is to be
removed from stable configuration
a. N
b. O ®
c. F
d. Ne
Ionization energy increases from left to right in period. Ionization energies of III-A and VI-A [O] show
abnormal trend.
a. B ®
b. C
c. N
d. O
a. N ®
b. O
c. S
d. P
Ionization energy increases from left to right in period. Ionization energies of III-A and VI-A [O] show
abnormal trend.
a. C > N > O
b. C < N < O
c. C < N > O ®
d. N > O > C
Ionization energy increases from left to right in period. Ionization energies of III-A and VI-A [O] show
abnormal trend
Which has the highest second ionization potential?
a. C
b. N
c. O ®
d. F
After removal of 1 electron, oxygen attains configuration of nitrogen (half filled p orbital)
a. Ionization energy ®
b. Electron affinity
c. Electronegetivity
d. Shielding effect
Elements having low ionization energy are metals. Elements having high ionization energies are non
metals while which have intermediate values are metalloids.
a. 2
b. 8
c. 10 ®
d. 7
a. Ionization energy
b. Electron affinity ®
c. Electronegetivity
d. SHielding effect
a. Zero ®
b. High
c. Positive
d. Negative
Stable electronic configuration and nucleus does not show attraction for extra electron
a. Nuclear charge
b. Atomic number
c. Atomic size
a. Alkali metals ®
c. Halogens
d. Oxygen family
Atomic radius decreases from left to right due to increase in nuclear charge. Thus electron affinity
increases from left to right. Thats why alkali metals have loewst and halogens have highest electron
affinity
E.A increases from Left to right but elements belong to V-A group[N] has low electron affinity generally
considered zero because they have stable configuration(half filled p orbital) so they do not gain electron
because if they do so them become unstale. VI > IV > III > V
a. Oxygen
b. Nitrogen ®
c. Carbon
d. Boron
a. B
b. N
c. Be
d. Cl ®
Electron affinities of halogens are F = 322, Cl = 349, Br = 324 and I = 295kj/mol. The higher value for Cl
as compared to F is :
b. Smaller electronegativity of F
In which of the following pairs of element, ist element of the pair has greater electron affinity
a. B, Al
b. N, P
c. S, O ®
d. F, Cl
As we move down a group from top to bottom electron Affinity becomes less negative because size of
atom increases . But Electron Affinity for third period elements i.e ( Al, P , S , Cl ) is more negative than
the second period elements i.e (B, N , O, F ) , This due to smaller size of the atoms of second period
elements which produce larger electron repulsion for addition of electron. Electron affinity and
ionization energy have opposite trend in 2nd and 3rd period
a. F
b. Cl ®
c. Br
d. I
a. Na
b. Mg
c. Al
d. Si ®
Electron affinity increases across periods. but elements belong to V-A[Si] group has low electron affinity
generally considered zero because they have stable configuration(half filled p orbital) so they do not
gain electron because if they do so them become unstale
a. O
b. O-
c. F-
d. Na
F- is already negatively charged and its octet is complete hence it is neutral, so eliminate that Na is
electropositive instead of accepting it will lose electrons, hence it is no incentive to add electrons,
eliminate this too Now between O and O-,O has the highest affinity towards electrons than O-. As the
size of atom decreases, a larger amount of energy is released when an elctrn is added to an isolated
gaseous atom. Among the given species, the size of O atom is smallest (Since, size of parent atom is
smaller as compared to its anion), thus its elctrn affinity is highest. Hence O is the correct answer.
Abdul Manan
CHEMICAL BONDING
London dispersion forces are significant for :
a. Polar molecules
c. Ionic solids
d. Metals
London dispersion forces can be present in both polar amd non polar molecules but significantly present
in non polar molecules. For example HCl is polar and has london disperson forces and dipole dipole
forces. He is non polar and has only london dispersion forces
Boiling point of higher alkanes are greater than those of lower alkanes due to the reason that:
In solid iodine, the distance between molecules of I2 is greater than gaseous I-I bond due to:
a. Strong forces
b. Weak forces
c. Rigidity
d. Polarizability ®
In the following metals which one has lowest probable interatomic forces?
a. Cu
b. Zn
c. Hg ®
d. Ag
Because mercury exist in liqued state its mean mercury has weaker forces
a. Ionic bonds
b. Hydrogen bonds
c. Vander waal' forces ®
d. Hydrophobic forces
Noble gases have Vander waal forces and they are non polar
a. He ®
b. HCl
c. NH3
d. H2O
a. He
b. CH4
c. CH3CH3
All molecules are non polar and have only london dispersion forces. Determine number of electrons per
unit. Greater the electrons per unit, greater the strength of london dispersion forces. He has 2e- per unit.
CH4 has 10e- per unit. CH3CH3 has 18e- per unit
Consider the substances Cl2, HCl, F2, and NaF, Which one has a (normal) boiling point closest to that of
argon?
a. Cl2
b. F2
c. HCl
d. NaF
Recognize that the most similar boiling points are predicted to be in the two substances that have the
most similar interparticle forces. Ion-ion forces are typically greater than any set of IM forces so NaF
should have a very high boiling point due to the ion-ion forces holding its “units” together. Its mean NaF
cannot be the right answer We know that noble gases have only london dispersion forces. Its mean that
answer(non polar molecule) would be right that also have only london dispersion forces. HCl have
london dispersion forces+ dipole dipole forces. Its mean it cannot be the right answer. Cl2 and F2 both
are non polar and have only London dispersion forces. Now check number of electrons per unit. London
forces will be stronger for more electrons/molecule. Ar and F2 have same number of electrons (18 e-).
Cl2 should have stronger IM forces than Ar or F2 because Cl2 have 34 electrons per unit
Which of the following would have highest boiling point at 1 atm pressure?
a. He
b. NaF ®
c. CH3OH
d. CH3CH3
Stronger the intermolecular forces, greater will be the boiling point. He and CH3CH3 have london
dispersion forces. CH3OH have hydrogen bonding. NaF have ion ion forces which are stonger than other
intermolecular forces
Which of the following would have highest vapour pressure at some hypothetical temperature?
a. He ®
b. NaF
c. CH3OH
d. CH3CH3
Weaker the strength of intermolecular forces, greater will be the vapour pressure. He and CH3CH3 have
london dispersion forces. He has weaker london dispersion forces as compared to CH3CH3 because He
has less number of electrons per unit. CH3OH have hydrogen bonding. NaF have ion ion forces which are
stonger than other intermolecular forces
a. Ionic bond
b. Metallic bond
c. Covalent bond
d. H-bond ®
Because it is formed due to inter atomic interaction. Vande waal < Dipole-dipole forces <H - bonding <
covalent < ionic < metallic
a. O-H
b. N-H
c. F-H ®
d. S-H
a. HF ®
b. HCl
c. HBr
d. HI
b. HF is weak acid
Which concept best explains that o-nitrophenol is more volatile than o-nitrophenol
a. Resonance
b. Hyper conjunction
c. Steric hinderence
d. Hydrogen bonding ®
o-nitrophenol has intramolecular hydrogen bonding while P-nitrophenol has intermolecular hydrogen
bonding so boiling point of p-nitrophenol is more
a. Chloroform
b. Ethyl alcohol
c. Acetic acid
d. Ethyl ether ®
a. Condensation reaction
b. Hydrogen bonding ®
a. Covalent
b. Coordinate
c. Hydrogen ®
d. Ionic
The maximum possible number of hydrogen bonds in which an H2O molecule can participate :
a. 1
b. 2
c. 3
d. 4 ®
Number of H - bond form by unpaired electrons of liquid NH3 , H2O and HF respectively are
(a) 3, 4, 2
(b) 4, 4, 2
(c) 3, 2, 1
(d) 1, 2, 1 ®
In Water oxygen atom has two lone pairs and two hydrogen atoms, meaning that the total number of
hydrogen bonds of a water molecule is up to four. In HF, each molecule has one δ+ hydrogen and three
active lone pairs. In the liquid as a whole, there are therefore three times as many lone pairs are there
are δ+ hydrogens. On average, then, each molecule can only form one hydrogen bond using its δ+
hydrogen and one involving one of its lone pairs. The other lone pairs are essentially wasted. Each
ammonia molecule can form one hydrogen bond using its lone pair and one involving one of its δ+
hydrogens. The other hydrogens are wasted.
a. H2O
b. HF ®
c. NH3
d. Acetic acid
H-bonds are maximum in number in water but their strength is weaker than H-bond in HF due to greater
E.N difference in HF
a. C6H5OH
b. C6H5COOH ®
c. CH3CH2OH
d. CH3COCH3
a. Intermolecular H-boding
b. Induced dipole
c. Permanent dipole
d. Debye
The force of attraction between CHCI3 molecules is permanent dipole due to being permanently polar
(due to having greater electro negativity difference), This is the reason why it exists as a liquid and
ofcourse London dispersion forces also present. Basically london dispersion forces are present in all
molecules whether they are polar or non polar
c. Debye forces
d. Instanteneous dipole
Chloroform has which type of forces?
a. H-bonding
Chloroform and acetone have significantly dipole dipole forces and of course London dispersion forces
are also present. But they are soluble in each other due to formation of hydrogen bond between them
DNA has two spiral chains. They are linked through H-bonding which is dominant between
a. C and H
b. O and H ®
c. N and H
d. N and O
a. Diomond
b. Ice
c. KCl
d. Neon(solid) ®
Which of the following compounds has an ionic, covalent and coordinate covalent bonds?
a. H2O
b. NH3
c. KBr
d. NH4Cl ®
Ionic bond between NH4+ and Cl-. Covalent between N and H to form NH3. Dative between NH3 and H+
to form NH4+
a. NaOH ®
b. KCl
c. CH4
d. SO2
Covalent bond is present between O-H and ionic bond is present between Na+ and OH-. KCl has ionic
bond. CH4 has London dispersion forces. SO2 is an angular molecule and hence polar, dipole-dipole
interactions work between its molecules along with London Dispersion Forces
a. 1, 3, 1 ®
b. 1, 3, 2
c. 1, 2, 3
d. 1, 1, 3
Ionic bond between NH4+ and Cl- Covalent bond between N and 3 H Coordinate
covalent between N and H
In hydronium ion, each bond shares
In which of the following the central atom form coordinate covalent bond:
a. BeCl2 ®
b. SiCl4
c. NCl3
d. CCl4
BeCl2 has linear structure and has polar covalant bond. In the solid, the BeCl2 molecules polymerise to
make long chains. They do this by forming coordinate bonds (dative covalent bonds) between lone pairs
on chlorine atoms and adjacent beryllium atoms
a. 1 ®
b. 2
c. 3
HNO3 has 1 coordinate covalent bond. Number of coordinate covalent bond in HClO2, HClO3, HClO4 are
1, 2 and 3 respectively between chlorine and oxygen. Number of coordinate covalent bonds is
determined by drawing dot and cross structure. Questions are given in your textbook exercise. I have
mentioned number of coordinate covalent bonds in compounds above as they are written in topic '
coordinate covalent bond'
Which of the following compound does not possesses coordinate covalent bond ?
(a) CO
(b) SO3
(c) HNO2 ®
(d) HNO3
H-O-N=O . CO and HNO3 have one one coordinate covalent bond. SO3 has two coordinate covalent
bond
a. Hydronium ion ®
b. Ammonium ion
c. Phosphonium ion
d. Carbonium ion
Any oxygen cation with three bonds called oxonium ion. H2O + H+ ------> H3O+
a. HF
b. HCl ®
c. CsF
d. LiF
(a) HCl
(b) CHCl3
(c) IF5
(d) KI
Electronegative difference in KI is more. Remainings have covalent bonds. HCl has polar covalent bond.
CHCl3 has polar covalent bond. IF5 has polar covalent.
a. NaCl
b. KCl
c. CaS ®
d. CsF
Lesser the E.N difference weaker will be the ionic compound NaCl,
KCl, CsF >>>> ionic bond between I-A and VII-A CaS >>>> ionic
bond between II-A and VI-A
3 and 6 electrons are present in valence shell of A and B respectively. The chemical formula of
compound :
a. A3B2
b. A2B3 ®
c. A2B
d. AB2
Which of the following molecules is nonpolar but has polar covalent bonds?
a. N2
c. H2O
b. H2O2
d. CCl4
In CCl4, C-Cl bond is polar due to E.N difference but C-Cl dipoles cancel each other so it is non polar
molecules. Similar is the case with CO2 which has C=O polar bond but molecule is non polar because
linear dipoles cancel each others. H2O2 has both polar and non polar bonds. N2 is a non polar molecule
and also have non polar covalent bond.
Which of the following molecule possesses polar and nonpolar covalent bond ?
(a) NH4Cl
(b) CCl4
(c) H2O2
(d) HCN
In H2O2 O-H polar and O-O non polar. CCl4 has only polar covalent bond. NH4Cl possess ionic,
covalent, dative bond.
a. CO2
b. BF3
c. CH4
d. CH3F ®
CO2 has polar C=O bond but molecule is non polar. CH4 is non polar. BF3 is non polar because it is
symmetrical and dipoles cancel each other. CH3Cl is a polar molecule due to the presence of a very
electronegative fluorine (3.98) as one of the outer atoms which pulls electrons towards it inducing a
partial negative charge.
a) LiF
b) NH3
c) CF4
d) HF
LiF (Lithium Fluoride) is an example of Ionic bond, as the formation takes place by transfer of electrons
and not by sharing.
Both nitrogen atoms have same electronegetivity in nitrogen molecule. It has an even charge
distribution between two nitrogen atoms. so it has zero polarity hence less tendency to break away and
form ions
a. High electro-negativity
a. 90° ®
b. 105°
c. 109°
d. 120°
Which has least bond angle?
a. CH4
b. H2O
c. NH3
d. BeF2
Which of the following molecule has one lone pair on central atom?
a. H2O
b. NH3 ®
c. CH4
d. PCl5
a. CO2 ®
b. CH4
c. NH3
d. H2O
a. H2S ®
b. CO2
c. C2H2
d. BeH2
H2O, H2S, H2Se, H2Te have similar geometry (bent or angular) and have 2 lone pairs+2 bond pairs
A molecule with two bond pairs and two lone pairs will have geometry:
(A) Tetrahedral
(C) Bent ®
Hydrides of III-A (AlH3, GaH3, InH3, TIH3) and halides of III-A (BCl3, BF3, AlCl3, AlF3 etc) have trigonal
planae geometry and have no lone pair+ 3 bond pairs. while NH3, NCl3, NF3, PH3 have trigonal
pyramidal geometry and have one lone pair+3 bond pairs
Central atom of the following has one lone pair and 3 bond pairs of electrons?
a. NH3 ®
b. AlCl3
c. BF3
d. H2S
Hydrides of III-A (AlH3, GaH3, InH3, TIH3) and halides of III-A (BCl3, BF3, AlCl3, AlF3 etc) have trigonal
planae geometry and have no lone pair+ 3 bond pairs. while NH3, NCl3, NF3, PH3 have trigonal
pyramidal geometry and have one lone pair+3 bond pairs. H2O, H2S, H2Se, H2Te have similar geometry
(bent or angular) and have 2 lone pairs+2 bond pairs
Which of the statement is correct about the shape of NH3 molecule
A) Square planer
B) Angular
C) Pyramidal ®
D) Tetrahedral
a. NH3
b. PH3
c. BF3 ®
d. PCl3
Hydrides of III-A (AlH3, GaH3, InH3, TIH3) and halides of III-A (BCl3, BF3, AlCl3, AlF3 etc) have trigonal
planar geometry and have no lone pair+ 3 bond pairs. while NH3, NCl3, NF3, PH3 have trigonal
pyramidal geometry and have one lone pair+3 bond pairs
(A) CH4
(B) BF3 ®
(C) NH3
(D) PH3
Hydrides of III-A (AlH3, GaH3, InH3, TIH3) and halides of III-A (BCl3, BF3, AlCl3, AlF3 etc) have trigonal
planar geometry and have no lone pair+ 3 bond pairs.
A) CCl4
B) NH3
C) BF3
D) H2O ®
H2O, H2S, H2Se, H2Te have similar geometry (bent or angular) and have 2 lone pairs+2 bond pairs
A) HgCl2 ®
B) NH3
C) BF3
D) H2O
H2O (104.5°) , NH3 (107.5°) , BF3 (120°) , HgCl2 (180°) , BeCl2 (180°)
(a) NH3
(b) SO2
(c) H2O
(d) H2S ®
A) MgCl2
B) BF4- ®
C) AlCl3
D) PCl5
MgCl2 (2e- pair system/AB2) , AlCl3 (3e- pair system/AB3) , BF4- (4e- pair system/AB4)
Which has the minimum bond angle:
(A) H2O
(B) H2S ®
(C) NH3
(D) NF3
Maximum bond angle can be reduced by replacing the ‘H’ in SbH3 with:
(A) O
(B) F ®
(C) Cl
(D) N
Substitution of hydrogen with electronegative atoms like F, Cl reduces bond angle. NH3 (107.5°) NF3
(102°). Hydrides of V-A (NH3, PH3, AsH3 , SbH3 , BiH3) have same geometry "trigonal pyramidal". The
bond pair in NH3 is close to N in N-H bond than the bond pair in P-H bond in PH3 . This is because the
size of the nitrogen is small than phosphorus . As a result , the force of repulsion between the bonded
pair of electrons in PH3 is more than in NH3 . Therefore the bond angle in PH3 molecule lesser than in
NH3 .
(A) CH4
(B) H2O
(C) NH3
(D) H2S ®
(A) SnCl2
(B) CS2
(C) ��2
(D) H2O ®
H2O, H2S, H2Se, H2Te have similar geometry (bent or angular) and have 2 lone pairs+2 bond pairs
(A) �- bond
(B) � - bond ®
(A )2 ®
(B) 3
(C) 4
(D) 5
a. 6 ®
b. 4
c. 5
d. 8
(B) Electronegativity
(C) Sizes of the bonded atoms
Bond length (inversly), E.N difference (directly), size of bonded atoms (directly)
a. N - O
c. N - Br
b. N - F ®
d. N - Cl
For Bond having two different elements , see their electronegativity difference. Greater the
electronegativity difference, greater the bond energy. For bond having same elements, see their sizes.
Greater the size of bonded atoms or atomic radii, greater the bond energy
a. H-H ®
b. C-C
c. N-N
d. O-O
For Bond having two different elements, see their electronegativity difference. Greater the
electronegativity difference, greater the bond energy. For bond having same atoms, see their sizes.
Greater the size of bonded atoms or atomic radii greater the bond energy. H-H > C-C > N-N > O-O
a. HF ®
b. HCl
c. HBr
d. HI
Greater the E.N difference, greater is the polarity
(A) HCl
(B) NH3
(C) H2O
(D) HF ®
For Bond having two different elements , see their electronegativity difference. Greater the
electronegativity difference, greater the bond energy and shorter the bond length. For bond having
same elements, see their sizes. Greater the size of bonded atoms or atomic radii, greater the bond
energy and shorter the bond length. F has the highest electronegtivity.
a. Electron diffraction
b. X ray diffraction
c. Spectral studies
d. Diffraction grating ®
Bond length of C-C and Cl-Cl is 154pm and 198pm respectively. What will be the bond length of C-Cl?
a. 176pm ®
b. 164pm
c. 117pm
d. 130pm
Generally the bond length between two atoms is approximately the sum of covalent radii of two atom.
Bond length of C-Cl = 154/2 + 198/2 = 77 + 99 = 176
a. 154pm
b. 139pm
c. 133pm ®
d. 120pm
a. C-C
b. Si-Si ®
c. N-N
d. P-P
For Bond having two different elements , see their electronegativity difference. Greater the
electronegativity difference, greater the bond energy and shorter the bond length. For bond having
same elements, see their sizes. Greater the size of bonded atoms or atomic radii greater the bond
energy and shorter the bond length As
bond length is sum of radii of two atoms and as we move from left to right in a row, radii decreases so
bond length decrease. Bond length increases down the group because atomic radius increases and
nuclear charge decreases down the group. Si-Si > P-P > C-C > N-N
a. C=C
b. C=N
c. C=O
d. N=O
If 2 elements belong to the same period then we check the electronegativity difference and bond length
is inversely proportional to electronegativity difference. Bond length of C=C is largest(134 pm) because
both the carbon atoms have same electronegativity. In case of C=O and C=N carbon is bonded to highly
electronegative atoms so bond length is shoreter as compared to C=C. In case of N=O oxygen is more
electronegative than nitrogen hence bond length decreases
Which of the following has been arranged in order of decreasing bond length?
a. P–O > S–O > Cl–O ®
For Bond having two different elements , see their electronegativity difference. Greater the
electronegativity difference, greater the bond energy and shorter the bond length. For bond having
same elements, see their sizes. Greater the size of bonded atoms, greater the bond energy and shorter
the bond length As bond length is sum
of radii ot two atoms and as we move from left to right in a row, radii decreases so bond length
decrease. Bond length increases down the group because atomic radius increases and nuclear charge
decreases down the group. E.N order F > O > Cl > P. As O and Cl both have high electronegativity so their
difference will be very low. S and O both belong to same group so they also have low E.N difference. P
and O belongs to different groups and also the different periods so have greater E.N difference
Since ionic bonds are non-directional, they don't exhibit space isomerism.
Although solid ionic compounds do not conduct electricity because there are no free mobile ions or
electrons, ionic compounds dissolved in water make an electrically conductive solution. In contrast,
covalent compounds do not exhibit any electrical conductivity, either in pure form or when dissolved in
water.
CHEMICAL ENERGETICS
What is the free energy change ∆G when 1 mol of water at 100°C and 1 atm pressure is converted to
steam at 100°C and 1 atm pressure?
a. 540 kcal
b. 9800 kcal
c. -9800 kcal
d. 0 kcal ®
At equilibrium ∆G = 0
a. Internal energy
b. Enthalpy
c. Entropy
d. Free energy ®
Energy required to dissociate 4g of gaseous hydrogen into free gaseous atoms is 208 kcal at 25°C. Bond
energy of H-H will be?
a. 104 kcal
b. 10.4 kcal
c. 208 kcal
d. 2.08 kcal
The bond dissociation energies of gaseous H2, Cl2 and HCl are 104, 58 and 103 kcal respectively. The
enthalpy formation of HCl gas would be
a. 44 kcal
b. - 44 kcal
c. 22 kcal
d. - 22 kcal
The H-H bond energy is 430 kj/mol and Cl-Cl bond energy is 240 kj/mol. ∆H for HCl is - 90 kj/mol. The H-
Cl bond energy :
a. 180 kj/mol
b. 360 kj/mol
c. 90 kj/mol
d. 425 kj/mol
If bond energies of H-H, Br-Br and H-Br are 433, 192 and 364 kj/mol respectively. The ∆H° for the
reaction H2(g) + Br2(g) -------> 2 HBr(g)
a. +261 kj/mol
b. - 261 kj/mol
c. +103 kj/mol
d. - 103 kj/mol ®
The heat of formation of CO(g) and CO2(g) are - 26.4 kcal and - 94 kcal respectively. The heat of
combustion of carbon
a. +26.4 kcal
b. - 67.6 kcal
c. - 120 kcal
d. +52.8 kcal
If enthalpies of methane and ethane are respectively 320 and 360 cal then bond energy of C-C :
a. 80
b. 40
c. 60
d. 120
a. 70
b. 100
c. 170
d. 270
C(g) + 4H(g) --------> CH4(g) ∆H= -166kj The bond energy C-H
a. - 208 kj/mol
b. - 41.6 kj/mol
c. 832 kj/mol
d. 166 kj/mol
CH4 has 4 C-H bonds so bond energy of single C-H = - 166/4 = - 41.6 kj/mol
Heat evolved in combustion of benzeneis given by C6H6 + 7½ O2 -----> 6 CO2 + 3 H2O ∆H = - 3264.6 kj.
How much energy will be evolved when 39g benzene are burnt
a. 816.15 kj
b. 1632.3 kj
c. 6528.2 kj
d. 2448.45 kj
78g benzene on combustion produces 3264.6 kj heat so 39g will produce 3264.6/2 = - 1632.3kj
The enthalpy of formation of ammonia is - 46 kj/mol. The enthalpy change for the reaction
2 NH3(g) --------> 2 N2(g) + 3 H2(g)
a. 46kj/mol
b. 92kj/mol ®
c. - 23 kj/mol
d. - 92 kj/mol
a. 44 kcal
b. 44000 kcal
c. 22 kcal
d. 11 kcal
When two moles of H2 and one mole O2 react together to form water, 484 Kj heat us evolved. What is H
formation for one mole of water?
a. - 484 kj/mol
b. - 242 kj/mol ®
c. +242 kj/mol
d. - 121 kj/mol
If bond enthalpy of N-H bond is x kj/mol, the value of enthalpy change in the process
a. 2x kj/mol
b. x kj/mol
c. 3x kj/mol ®
d. x/3 kj/mol
In NH3 there are three N-H bonds. For one N-H, bond enthalpy is x kj/mol. So for 3 N-H, bond enthalpy
will be 3x kj/mol
Heat of combustion of CH4, C2H6, C2H4 and C2H2 are - 212.8, - 373, - 337, and - 310.5 kcal respectively
at same temperature. The best fuel among these gases is
a. CH4
b. C2H4
c. C2H6
d. C2H2
The fuel should have high calorific value. Higher the calorific value, best will be the fuel. CH4 has high
caloric value - 212/16 = - 13.3 kcal/g
A mixture of 2 moles of CO and 1 mole of oxygen, in a closed vessel is ignited to convert CO to CO2. If ∆H
is the enthalpy change and ∆E is the change in internal energy then
a. ∆H > ∆E
b. ∆H < ∆E ®
c. ∆H = ∆E
Consider the reaction N2 + 3H2 ------> 2NH3 Carried out at constant temperature and pressure. If ∆H
and ∆E are enthalpy and internal energy changes for the reaction, which expression from given is true
a. ∆H > ∆E
b. ∆H < ∆E ®
c. ∆H = ∆E
d. ∆H = 0
At constant P or T ∆H = ∆E + ∆nRT [ ∆n = 2 - 4 = - 2]
a. + 874 kj
b. - 874 kj
c. - 871 kj
d. - 876 kj
The change in heat energy of a chemical reaction at constant temperature and pressure is called
a. Enthalpy change ®
b. Bond energy
d. Heat of sublimation
For a given process, the heat changesbat constant pressure (Qp) and at constant volume (Qv)are related
to each other
a. Qp = Qv
b. Qp < Qv
c. Qp > Qv ®
d. Qp = Qv/2
a. Entropy
b. Enthalpy ®
c. Temperature
d. Internal energy
The relation between change in internal energy ∆E, change in enthalpy ∆H and work done W :
a. ∆H = ∆E + W ®
b. ∆E = ∆H + W
c. ∆E = W - ∆H
d. W = ∆E - ∆H
a. 0 at 298K
b. 1 at 298K
c. 0 at all temperatures
d. 0 at 273K
b. Negative ®
c. Zero
d. Cannot be predicted
A) Heat of solution
B) Heat of combustion
C) Heat of neutralization
D) Heat of atomization ®
The enthalpy of neutralization of which of the following acids and bases is equal to - 13.6 kcal
Option B and option C both are correct. But option B is more accurate because NaOH is slightly stronger
base than KOH
Heat of neutralization for the given reaction NaOH + HCl -----> NaCl + H2O is 57.1 kj/mol. What will be
the heat released when 0.25 mole of NaOH is titrated against 0.25 mole of HCl
a. 57.1 kj/mol
b. 22.5 kj/mol
c. 14.3 kj/mol
d. 28.6 kj/mol
A) Non-spontaneous reaction
a. Enthalpy of combination
b. Enthalpy of reaction
c. Enthalpy of formation ®
d. Enthalpy of fusion
Enthalpy of formation is the change of enthalpy when one mole of the compound is formed from atoms
of its elements
a. Heat of formation
b. Heat of reaction ®
c. Heat of combustion
d. Heat of neutralization
It cannot be combustion because in combustion carbon is burnt in presence of oxygen. It cannot be heat
of formation because in formation there is one mole compound is formed from its elements in their
most stable state like C(graphite. s) + 2H2(g) ------> CH4(g) Stable states of graphite, hydrogen and
methane are solid, gas and gas. Or you can say that enthalpy of formation is The change of enthalpy
when one mole of the compound is formed from atoms of its elements.
b. Enthalpy of reaction
c. Enthalpy of combustion
d. Enthalpy of solution
The heat change for the reaction is H2(g) + ½O2(g) -------> H2O(l)
a. Heat of reaction
b. Heat of formation
c. Heat of vapourization
d. Heat of solution
The heat change for the reaction is 2CO + O2 -------> 2 CO2 ∆H = - 135 kcal
a. Heat of formation
b. Heat of combustion ®
c. Heat of solution
d. Heat of reaction
a. H2O + CO2 ®
b. CO2 + H2
c. COCl2
d. CO + CO2 + H2O
Hesses law of constant heat summation is based on
a. Conservation of mass
b. E = mc²
a. Heat of formation
b. Heat of combustion
c. Indirect measurement of H
d. All of these ®
Which of the following values of heat of formation indicates that product is least stable?
a. - 94 kj
b. - 213 kj
c. +21.4 kj
d. +70 kj ®
a. - 393.7 kj ®
b. +393.7 kj
c. +172.7 kj
d. - 172.7 kj
a. 714.8 kj/mol
b. +1.9 kj/mol ®
c. - 1.9 kj/mol
d. 0
a. Crystal energy
b. Lattice energy
c. Electron affinity
d. All ®
Born Haber cycle is application of
B) Rate law
C) Hess’s law ®
D) Equilibrium law
Which of the following is not necessary for calculating lattice energy of KBr?
a. Enthalpy of Ionization of Br ®
b. Enthalpy of atomization of K
c. Enthalpy of atomization of Br
a. 787 kj/mol
b. 399 kj/mol
c. 289 kj/mol
d. 312 kj/mol
a. - 604 kj/mol
b. - 704 kj/mol
c. - 504 kj/mol
d. - 667 kj/mol
a. NaCl ®
b. NaBr
d. NaI
Lattice energy of an ionic compound depends upon charge densities of ions. Greater the charge density
greater will be the lattice energy. Charge density = charge/size
a. Ionization potential
b. Electron affinity
c. Electronegetivity
d. Lattice energy ®
Electron affinity is the measure of attraction of nucleus of an atom for extra electron
ELECTROCHEMISTRY
Reduction reaction means ________
(a) Al ®
(b) Cr2O3
(c) Al2O3
(d) Cr
On left side, Al has zero oxidation state. On right side Al has +2 oxidation. Increase in oxidation means
substance has get oxidized. Al° ------> Al+² Cr+² ------> Cr°
(a) Al ®
(b) Cr2O3
(c) Al2O3
(d) Cr
"Reducing agent reduces others but itself oxidize" Al° ------> Al+² Cr+² ------> Cr°
a. Ca(s) ®
b. Zn(s)
c. Ca+²(aq)
d. Zn+²(aq)
Reducing agent reduces other while itself get oxidized. Oxidation means increase in oxidation state
In ist equation, oxidation state of Cu changes from 0 to +2 so it is oxidized. Oxidation state of N changes
from +5 in HNO3 to +4 in NO2 so it is reduced In second
equation, oxidation state of Mg changes from 0 to +2 and of oxygen changes from 0 to - 2 . Hence Mg is
oxidized while oxygen is reduced. In 3rd equation,
oxidation state of Mg changes from 0 to +2 and of hydrogen changes from +1 to 0. Hence Mg is oxidized
and H is reduced In 4th equation,
oxidation state of Mg changes from +2 to +1 hence it is reduced. Oxidation state of O, Cl and H does not
change.
In the second equation, oxidation number of H in H2 (0) decreases to -1 in C2H6, while oxidation
number of C in C2H4 (+2) increases to +3 in C2H6
(A) +2
(B) +4
(C) +2.5 ®
(D) +6
(A) - 1
(B) +1 ®
(C) +2
(D) - 2
(A) SO2
(B) H2SO4
(C) H2S ®
(D) Na2SO4
+4 , +6 , - 2 , +6 are the oxidation states of sulphur in SO2, SO3, H2S and Na2SO4 respectively
a. +4
b. - 4
c. +3
d. +5 ®
(a) +8
(b) +7
(c) +5
(d) +6 ®
Charge on SO4 is -2 . There are three SO4 so charge will be - 6. Hence charge on Al2 should be +6. Its
mean oxidation state of Al is +3 SO4-² : O.S of S
+ O.S of oxygen = - 2 ----> O.S of S + 4(-2) = - 2 ----> O.S of S = +6
Which of following elements does not possess positive oxidation no. in any of its compound ?
(a) O
(b) F ®
(c) Cl
(d) I
F always shows -ve oxidation state. O shows +ve oxidation in one of its compound OF2
Which of the following oxidation no. does not possess by Cl, Br and I, when they combines with oxygen
forming chemical bond ?
(a) +1
(b) +3
(c) +5
(d) –1 ®
Except F, all others halogen does not -ve oxidation state when combine with halogens. Example : In
NaBrO3 , Br has +5 oxidation state. In OF2, F has - 1 oxidation state
Oxygen conbines with which of the element by forming chemical bond, then it possesses positive
oxidation no. ?
(a) F ®
(b) Cl
(c) Br
(a) F
(b) Ca
(c) Cs ®
(d) O
a. 0 ®
b. 1
c. 2
d. 4
a. +1
b. - 1 ®
c. +2
d. - 2
+2 + 2x = 0 ------> x = - 1
a. - 1 ®
b. +1
c. - 2
d. +2
a. 0 to - 2
b. 0 to - 3 ®
c. 0 to 0
d. 2 to 5
a. +5 ®
b. - 5
c. +3
d. - 3
3(+1) + x - 8 = 0 -------> x = +5
a. SO2
b. SO3
c. H2S
d. H2SO3
+4 , +6 , - 2 , +4 are the oxidation states of sulphur in SO2, SO3, H2S and H2SO3 respectively
a. +4
b. +6 ®
c. +5
d. - 6
x - 8 = - 2 ------> x = +6
a. +2 to +3
b. +12 to +3
c. +7 to +3
d. +6 to +3 ®
2(+1) + 2x - 14 = 0 -------> x = +6
a. Oxidation
b. Reduction
c. Redox ®
d. Decomposition
Iron is oxidized as its oxidation state changes from 0 to +3 while chlorine is reduced as its oxidation state
changes from 0 to - 3
What mole of MnO4- reduced in Mn2+ by the addition of 7.5 mole electrons in MnO4- ?
(a) 2.5
(b) 5
(c) 1.5 ®
(d) 7.5
oxidation state of Mn in MnO4- is +7 and oxidation state of Mn^2+ is +2
Difference of charge = +5 . Its mean 5 mole of electrons should be added to MnO4- to reduce its
one mole into Mn+2 5 mol
of e- >>>> reduces 1 mol of MnO4- 1 mol
of e- >>>> reduces 1/5 mol of MnO4- 7.5 mol of e-
>>>> reduces 7.5/1.5 mol of MnO4-
a. 1F
b. 3F
c. 4F
d. 6F
a. 2
b. 3
c. 4
d. 5
In this equation, all the atoms are balanced. For balancing electrons, add 3e- to left side NO3-
+ 4H+ + 4e- -------> 2 H2O + NO
In balancing the half reaction : S2O3-² --------> S(s) the number of electrons that must be added
a. 4 on left side ®
b. 3 on right side
c. 2 on left side
d. 2 on right side
4e- + S2-² --------> 2S° As change in oxidation state of S is +2. Hence number of electrons that
must be added are 4
How many electrons are required to balance the charge in the following equation:
2 Cr+³ + 7H2O -------> Cr2O7-² + 14H+
The overall charge of the reactants is +6 because of the 2Cr+³ . The overall charge of the products is +12,
because of the 14H+ and the one Cr2O7-² . Therefore, we add 6 electrons to the reactants so that both
sides are +6 [Information from given
reaction : Cr2O7-² has 7 oxygens, we added 7 water molecules to the reactants to balance atoms of
oxygen. Because of the 7 water molecules we added, we need 14 hydrogen ions to balance hydrogen
atoms on product side]
What is the coefficient for hydroxide for balancing the reaction? Pb(OH)4-² +
ClO- ----> PbO2 + Cl- + OH- + H2O
a. 1 OH-
b. 2 OH-
c. 3 OH-
d. 4 OH-
Always take start from lower cofficient. Suppose we take 1 coefficient of OH- (and balance H) Pb(OH)4-²
+ ClO- ----> PbO2 + Cl- + 1OH- + H2O Now you
cannot balance H and O. So leave this option Suppose we take 2
coefficient of OH (and balance H) Pb(OH)4-² + ClO- ---->
PbO2 + Cl- + 2OH- + H2O Now hydrogen and
oxygen are balanced
a. +3.87 V
b. - 3.87 V
c. +2.87 V ®
d. - 2.87 V
a. K ®
b. Mg
c. Al
d. I
Elements lie on the top of the electrochemical series are strong reducing agent
a. Au
b. Al ®
c. Hg
d. Ag
Only those metals can displace hydrogen from acids that lie above SHE in electrochemical series.
a. Fe
b. Cu
c. Al ®
d. Hg
Only those metals can displace hydrogen from acids that lie above SHE in electrochemical series.
Which can displace hydrogen from acids?
a. K ®
b. Pt
c. Pd
d. Cu
a. Zn + H2SO4(dil)
b. Cu + H2SO4(dil)
c. Mg + H2SO4(dil)
d. Zn + HCl(dil)
Metals like Au, Ag, Pt and Cu which have sufficiently high positive values of reduction potentials do not
liberate hydrogen from acids and they lie below SHE in electrochemical series
Which of the following metals cannot evolve H2 from acids or H2O or from its compounds
a. Hg ®
b. Pb
c. Al
d. Fe
Only those metals can displace hydrogen from acids that lie above SHE in electrochemical series. Hg has
greater reduction potential than H+ and hence cannot displace it from acid
a. Fe
b. Hg
c. Au
d. Ag
An element can replace other element if that element lies above other elements in series. Iron is placed
above Cu in Electrochemical series so Cu cannot replace iron.
a. B
b. C
c. D
d. None
An element can replace other element if that element lies above other elements in series. An element
has minimum(negative) reduction potential value which lie on the top. A is displace from D because D
has E° = - 0.402V
Which of the following metal can deposit copper from copper sulphate solution
a. Mercury
b. Iron ®
c. Gold
d. Platinum
An element can replace other element if that element lies above other elements in series. Iron is placed
above. Iron lies above Cu so Cu+² will be reduced and Fe will be oxidized
The standard electrode potentials of four metals A, B, C and D are - 1.2V , 0.6V , 0.85V and - 0.76V
respectively. The sequence of deposition of metals on applying potential is:
a. A, C, B, D
b. B, D, C, A
c. C, B, D, A ®
d. D, A, B, C
Elements lie above SHE are stronger reducing agent and elements lie below SHE are stronger oxidizing
agent. Higher the element in series, more easily can be deposited C < B < D < A
Four alkali metals A, B, C and D are having respectively standard electrode potential as - 3.05V, - 1.66V ,
0.4V , 0.8V. Which one will be the most reactive?
a. A ®
b. B
c. C
d. D
More negative is the standard potential, greater is the trendency to lose electrons and has greater
reactivity
a. Copper
b. Silver
c. Iron ®
d. Nickel
Which of the following metal does not react with solution of copper sulphate?
a. Mg
b. Fe
c. Zn
d. Ag ®
An element can replace other element if that element lies above other elements in series. Iron is placed
above. As Ag lies below Cu so it does not react.
a. Na+
b. Al+³
c. Zn+²
d. H+ ®
Down the electrochemical series, reduction potential increases and strength of oxidizing agent increases.
Oxidizing agent oxidize others and get reduce itself. So down the series, electron gaining power
(reduction process) increases.
a. Al ®
b. Ca
c. Na
d. K
Down the electrochemical series, reduction potential increases and strength of oxidizing agent increases.
Oxidizing agent oxidize others and get reduce itself. From given options only Al lies below Mg. Its mean
Al is stronger oxidizing agent
a. Li ®
b. Na
c. K
d. Cs
Upgoing electrochemical series, resuction potential decreases and strength of reducing agent increases.
So elements that lie on top of the series are stronger reducing agent
The standard reduction potential for Li+/Li ; Zn+²/Zn ; H+/H and Ag+/Ag is - 3.05 , - 0.762 , 0.00 and
+0.80 V. Which has highest reducing capacity?
a. Ag
b. Zn
c. H2
d. Li
Upgoing electrochemical series, resuction potential decreases and strength of reducing agent increases.
So elements that lie on top of the series are stronger reducing agent. OR you can say that Li has
negative(minimum) reduction potential and has maximum trendency to lose electron(strongest
reducing agent)
a. Li
b. Cu
c. Au ®
d. Al
The element which can displace three other halogens from their compound is
a. Cl
b. F ®
c. Br
d. I
K, Ca and Li metals may be arranged in the decreasing order of their standard electrode potentials
a. K, Ca, Li
b. Ca, K, Li ®
c. Li, Ca, K
d. Ca, Li, K
Down the electrochemical series, standard electrode potential increases so Standarf electrode potential
of Ca > K > Li
On which of the following cell potential of the cell does not depend?
(a) temperature
The standard reduction potential NaCl for the half reactions are as
Zn = Zn+² + 2e- E° = 0.76 V and Fe = Fe+² + 2e- E° = 0.41 V
The emf for the cell reaction Fe+² + Zn -------> Zn+² + Fe
a. - 0.35 V
b. + 0.35 V
c. + 1.17 V
d. - 1.17 V
Metal lies above SHE acts as anode and metal lies below SHE acts an cathode. If both metals given in
questions lie above or below the SHE then emf of cell can be determined by equation E° = Ecathode -
Eanode . In these cases take reduction potentials of both metals. Fe and Zn both lies above SHE. We
know that metals lie above SHE have -ve reduction potentials. According to equation Fe is acting as
cathode(reduction) and Zn is acting as anode(oxidation) Emf = Ecathode - Eanode = -
0.41 - (-0.76) = +0.35
Standard reduction potential for Fe+²/Fe and Sn+²/Sn electrodes are - 0.44V and - 0.14V respectively.
For the cell reaction Fe+² + Sn -------> Fe + Sn+²
a. +0.30V
b. - 0.30V
c. +0.58V
d. - 0.58V
Metal lies above SHE acts as anode and metal lies below SHE acts an cathode. If both metals given in
questions lie above or below the SHE then emf of cell can be determined by equation E° = Ecathode -
Eanode . In these cases take reduction potentials of both metals. Fe and Sn both lies above SHE. We
know that metals lie above SHE have -ve reduction potentials. According to given equation Fe is acting
as cathode(reduction) and Sn is acting as anode(oxidation) Emf = Ecathode - Eanode = -
0.44 - (-0.14) = - 0.30
The emf of galvanic cell with electrode potentials of silver = +0.80V and that of copper = +0.34V is
a. - 1.1 V
b. 1.1 V
c. 0.46 V
d. 0.76 V
If both metals given in questions lie above or below the SHE then emf of cell can be determined by
equation E° = Ecathode - Eanode. In these cases take reduction potentials of both metals. Silver and
copper both lie below SHE. We know that metals lie below SHE have +ve reduction potential values.
Metal lies above SHE acts as anode and metal lies below SHE acts an cathode. But in question both
metals lie below SHE. So take that metal as cathode that lie below the other. Its mean silver will act as
cathode and copper will act as anode E = Ecathode - Eanode = 0.80 - (+0.34) =
0.46V
a. - 2.03V
b. 1.36V
c. 2.7V
d. 2.03V
Metal lies above SHE acts as anode and metal lies below SHE acts an cathode. If one metal given in
question lies above SHE and other lies below SHE then emf can be find out as E° = Ecathode + Eanode .
In this case take reduction potential of cathode and oxidation potential of anode. Mg lies above SHE so
will act as anode. Take its oxidation potential value. Cu lies below SHE so will act as cathode. Take its
reduction potential value. We know that metals lie above SHE have -ve reduction and metals lie below
SHE have positive reduction potentials. We also know that oxidation and reduction potential values of a
metal are same but with opposite sign. E = Ecathode + Eanode = - 0.34 + (+2.37) = 2.71V
a. 2.95V
b. 3.0V ®
c. 3.03V
d. 0.31V
Metal lies above SHE acts as anode and metal lies below SHE acts an cathode. If one metal given in
question lies above SHE and other lies below SHE then emf can be find out as E° = Ecathode + Eanode. In
this case take reduction potential of cathode and oxidation potential of anode. Al lies above SHE so will
act as anode. Take its oxidation potential value. Cl lies below SHE so will act as cathode. Take its
reduction potential value. We know that metals lie above SHE have -ve reduction potential values and
metals lie below SHE have positive reduction potentials. We also know that oxidation and reduction
potential values of a metal are same but with opposite sign. E = Ecathode + Eanode = 1.36 + (+1.67) = 3V
The standard electrode potentials of Zn+²/Zn and Ag+/Ag are - 0.763V and +0.799V respectively. The
standard potential of cell
a. 1.56 V
b. 0.036 V
c. - 1.56 V
d. 0.799 V
Metal lies above SHE acts as anode and metal lies below SHE acts an cathode. If one metal given in
question lies above SHE and other lies below SHE then emf can be find out as E° = Ecathode + Eanode .
In this case take reduction potential of cathode and oxidation potential of anode. Zn lies above SHE so
will act as anode. Take its oxidation potential value. Ag lies below SHE so will act as cathode. Take its
reduction potential value. We know that metals lie above SHE have -ve reduction and metals lie below
SHE have positive reduction potentials. We also know that oxidation and reduction potential values of a
metal are same but with opposite sign. E = Ecathode + Eanode = 0.799 + (+0.763) = 1.56V
A galvanic cell with electrode potential of A' = +2.33V and B' = -1.43V . The value of E° cell is
a. 3.66V
b. 0.80V
c. - 0.80V
d. - 3.66V
Metal lies above SHE acts as anode and metal lies below SHE acts an cathode. Metals lie above SHE has -
ve reduction potential values and metals lie below SHE have +ve reduction potential values. Its mean A
will acts as cathode and B will acts as anode. If one metal given in question lies above SHE and other lies
below SHE then emf can be find out as E° = Ecathode + Eanode. In this case take reduction potential of
A(cathode) and oxidation potential of B(anode). We also know that oxidation and reduction potential
values of a metal are same but witj opposite sign. E = Ecathode + Eanode = 2.33 + (+1.43) =3.66V
a. Zn|Zn+²||Cu+²|Cu ®
b. Cu|Cu+²||Zn+²|Zn
c. Cu|Zn+²||Zn|Cu+²
d. Cu+²|Zn||Zn+²|Cu
Electrode on which oxidation occurs is written on L.H.S and the other on R.H.S
Which of the following reactions is not feasible according to the electrochemical series?
(A) 2H2O + F2 ------> 4HF + O2
The reactions are based on the reactivity order of halogens F > O > Cl > Br > I Reaction C is
not feasible since iodine cannot displace Br due to its less reactivity. If you have any confusion, plz
concern topic "properties of halogen" in 2nd year chemistry. Read about oxidizing power of halogens
a. Feasibility of reaction
2H+(aq) + 2e- -------> H2(g) The standard electrode potential for the above reaction
a. 0 ®
b. 1
c. - 1
d. 0.67
a. ZnCl2
b. HgCl2
c. Hg2Cl2
d. CuSO4
Calomel electrode is a type of half cell in which the electrode is mercury coated with calomel (Hg2Cl2)
and the electrolyte is a solution of potassium chloride and saturated calomel
a. Oxidation
b. Reduction
c. Redox
d. Oxidation or reduction ®
a. Oxidation ®
b. Reduction
c. Redox
d. Oxidation or reduction
SHE becomes anode and Cu-electrode becomes cathode because reduction potential of Cu is greater
than SHE i.e lies below SHE
A solution of sodium sulphate in water is electrolysed using inert electrodes. The products at the
cathode and anode are respectively:
a. H2 , O2 ®
b. O2 , H2
c. O2 , Na
d. H2 , SO2
In water available ions are Na+ , SO4-² , H+ and OH- . As reduction potential of H+ is higher than that of
Na+, so it reduces at the cathode and H2 liberates. and As oxidation potential of OH- is higher than that
of SO4-² so it oxidises at the anode and O2 liberates.
During electrolysis of aqueous CuSO4, products at cathode and anode are respectively :
a. Cu , O2 ®
b. Cu , SO2
c. H2 , O2
d. H2 , SO
In water available ions are Cu+² , SO4-² , H+ and OH- . As reduction potential of Cu+² is higher than H+ so
it reduces at cathode and liberate Cu and As oxidation potential of OH- is higher than that of SO4-² so it
oxidises at the anode and O2 liberates.
During electrolysis of aqueous CuCl2, products at cathode and anode are respectively :
a. Cu , O2 ®
b. Cu , Cl2
c. H2 , O2
d. H2 , Cl2
In water available ions are Cu+² , Cl- , H+ and OH-. As reduction potential of Cu+² is higher than H+ so it
reduces at cathode and liberate Cu and As oxidation potential of Cl- is higher than that of OH- so it
oxidises at the anode and Cl2 liberates.
For aqueous KNO3, aqueous NaOH, aqueous H2SO4, aqueous ZnSO4 and aqueous Na2SO4 we get H2
on cathode and O2 at anode
During electrolysis of dilution KNO3, which of them is collected at anode?
A) H2
B) K
C) O2 ®
D) N2
For aqueous KNO3, aqueous NaOH, aqueous H2SO4, aqueous ZnSO4 , aqueous NaCl and aqueous
Na2SO4 we get H2 on cathode and O2 at anode
a. H2 gas at cathode ®
b. H2 gas at anode
O2 and Cl will compete for anode. Because the anode is positively charged and as oxygen is strongly
electronegative (having a negative charge) it would solely be attracted to the positive electrode if this
was electrolysis of pure water (remember, that opposite charges attract), but because Chlorine is even
more strongly electronegative it is preferentially attracted to the anode and released there
a) HCL
b) Acetic acid
c) Propinoic acid
d) H2SO3
The strong electrolyte is HCL because it is strong acid and acts as electrolyte. The acetic acid, propinoic
acid and H2SO3 are weak acid electrolytes
b. Light energy
c. Electrical energy ®
d. Heat energy
b. Daniel cell
d. H2 - O2 cell ®
a. KOH ®
b. NaNO3
c. Aqueous NaCl
d. Aqueous H2SO4
b. it is a secondary cell
In hydrogen-oxygen fuel cell, the two electrodes are hollow tube made of porous compressed carbon
impregnated with platinum which act as?
(A) Inhibitor
(B) Reducing agent
(C) Catalyst ®
______________ and suitable catalyst are required to promote high rate of electrode processes.
a) Lower temperature
b) Higher temperature
c) Moderate temperature
Higher temperature and suitable catalyst are required to promote the high rate of electrode processes.
The reaction at the anode produces electricity and water as by-products. The catalyst lowers the
activation energy required, allowing the reaction to proceed more quickly or at a lower temperature.
a) Hydrogen peroxide
b) Alcohol
c) Water
d) Potassium permanganate
The residual product discharged by the hydrogen-oxygen cell is water. It is formed by the oxidation
reaction taking place at electrodes and combining the hydrogen and oxygen molecules.
a. Equal
b. Constant ®
c. Maximum
d. Minimum
a. Ka
b. Kc
c. Kp ®
d. Kx
Kc = [products]/[reactants]
b. Presence of a catalyst
For the reaction, H2(g) + I2(g) < ----- > 2HI(g) the equilibrium constant Kp changes with
a. Temperature ®
b. Pressure
c. Catalyst
d. Concentration of H2 and I2
For a reaction A + B < ------ > C + D when we start with 2 moles of each A and B, Kc = 25. What will be
the value of Kc If we start with 1 mole of each A and B?
(a) 25 ®
(b) 5
(c) 12.5
(d) 50
Kc depends on temperature and concentration of reactants at equilibrium. Kc does not depend upon
initiall concentration of reactants, Pressure or volume, Direction of reaction, Catalyst
For a reversible reaction, if the concetration of the reactants are doubled, the equilibrium constant will
be
(b) Halved
(c) Doubled
According to Le-chatllier principle, if conc. of reactants become doubled then forward reaction takes
place and conc. of products also increase so equilibrium constant also remain same Kc depends on
temperature and concentration of reactants at equilibrium. Kc does not depend upon initiall
concentration of reactants, Pressure or volume, Direction of reaction, Catalyst
The equilibrium constant for a reaction is 4.4×10-⁴ at 2000k. In presence of a catalyst, equilibrium is
attained ten times faster. Therefore the equilibrium constant,in presence of catalyst at 2000K is........
a. 4.4×10-³
b. 4.4×10-^5
c. 4.4×10-⁴ ®
d. Difficult to compute
Kc depends on temperature and concentration of reactants at equilibrium. Kc does not depend upon
initiall concentration of reactants, Pressure or volume, Direction of reaction, Catalys
The following reaction was allowed to reach state of equilibrium 2A + B < ------- > C The initial amounts
of the reactants present in 1dm³ of solution were 0.5 mol of A and 0.6 mol of B. At equilibrium the
amounts were 0.2 mol of A, 0.45 mol of B and 0.15 mol of C. Calculate equilibrium constant Kc?
a. 8.3 ®
b. 7.8
c. 6.6
d. 9.1
Kc = [C]/[A]²[B] Put the values of concentrations which are present at equilibrium stage
1g mole of ethyl alcohol and 1g mole of acetic acid are mixed. At equilibrium 0.666g mole of ester is
present. The value of equilibrium constant is
a. ¼
b. ½
c. 2
d. 4
Consider the following gaseous reaction system having partial pressure at equilibrium
2HI < -------- > H2 + I2
100 torr 50 toor 50 torr
a. 1
b. 0.5
c. 0.25 ®
d. 0.75
Kp = 50×50/(100)² = 0.25
When the equilibrium concentration of both reactants is 0.5 M each, the value of Kp under same
condition will be: H2 + I2 < ------ > 2 HI
(a) 125
(b) 50 ®
(c) 75
(d) 100
Kp = [HI]²/[H2][I2] = 0.5×0.5/2
A vessel contains CO2at 1000k temperature with a pressure 0.5 atm.some of CO2 is converted in to CO
on addition of graphite. If total pressure at equilibrium is 0.8 atm the value of KPis:
(a) 3 atm
a. Pressure
b. Temperature
c. Concentration
d. Catalyst ®
a. Catalyst
b. Pressure
c. Volume
d. Temperature
For endothermic reaction ( ∆H > 0), change in temperature affects the equilibrium system and forward
reaction takes place with increase in temperature
Which of the following equilibrium is not affected by change in volume of the flask?
Change in volume affects number of moles per unit volume. In third reaction moles of reactants = moles
of products so volume change does not affect equilibrium
In a given system, water and ice are in equilibrium. If pressure is applied to the above system, then,
Pressure on equilibrium system increases, so volume decreases. Volume of ice is more than liqued H2O
so more ice is melted
What will be the direction of reversible reaction when one of the product of the reaction is removed?
(d) At equilibrium
For the following reaction in gaseous phase CO + ½O2 < ------ > CO2 Kc/Kp is:
a. (RT)½
b. (RT)-½ ®
c. RT
d. (RT)-¹
a. Synthesis of NH3
b. Dissociation of HI ®
c. Formation of SO3
d. Dissociation of PCl5
c. 2x/(1-x)² d. 4x²/(1-x)V
a. 10-³°
b. 10³° ®
c. 1
d. 0
Kc = [products]/[reactants]
a. 100 atm
b. 200-300 atm ®
c. 600 atm
d. 1000 atm
Ammonia is removed from equilibrium mixture by which method in Haber's process?
a. Cooling ®
b. Heating
c. Filtration
d. Decomposition
(A) 10%
(C) 13% ®
(B) 16%
(D) 25%
a. mol-¹ L-¹
b. mol-² L-²
c. mol-² L-¹
d. mol² L-² ®
d. Temperature is increased ®
When H+ ions added they combine with OH-. In this way [OH-] decreases hence Kw decreases. Same is
the case when OH- ions are added
On adding ammonia to water
On adding ammonia OH- will decrease and in result [H3O+] will increase in order to keep Kw constant
a. 14 ®
b. 7
c. 10-¹⁴
d. 10¹⁴
a. 10-¹⁴ mole/dm³ ®
b. 14 mole/dm³
d. 1 mole/dm³
pH of rain water
a. 5
b. 6
c. 6.2 ®
d. 7
pH of a solution is 9, the solution is
a. Weak acid
b. Weak base ®
c. Strong acid
d. Strong base
a. Acidic
b. Basic ®
c. Neutral
d. Cannot be predicted
a. 0.1M NaOH
b. 0.1M KOH
c. 0.1M HCl ®
d. 0.1M HF
Equimolar solution of the following were prepared in water separately. Which one of the solutions will
record the highest pH?
a. SrCl2
b. BaCl2
c. MgCl2
d. CaCl2
All alkaline earth metal chlorides (MCl2) on hydrolysis produce acidic solution. Down the group acidic
character decreases so BaCl2 will have highest pH
a. 0.5M HCl
b. 0.5M H2SO4
c. 0.1M HNO3
d. 0.5M CH3COOH
Remember: log 1 = 0 . [H+] is 1 in case of 0.5M H2SO4 because it is diprotic acid hence [H+] = 2×0.5M =
1 >>>> pH = - log 1 = 0
The pH of a solution is 5. To this solution, sufficient acid was added and its pH decreases to 2. The
increase in [H+] is
a. 10 times
b. 3 times
c. 100 times ®
d. 1000 times
a. 3
b. 4
c. 11
d. 10
a. 2
b. 12
c. 3
d. 11
a. 8
b. - 8
c. 6 ®
d. - 6
pH + pOH = 14
The pH of an aqueous solution of a 0.1M solution of a weak monoprotic acid which is 1% ionized:
a. 1
b. 2
c. 3
d. 14
0.1M = 10-¹ M , % ionization = 1% = 1/100 = 10-² [H+] = 10-² × 10-¹ = 10-³ pH = - log [H+] =
- log 10-³ = 3 log 10 = 3
a. 3.7
b. 10.3
c. 4
d. 10
a. 3
b. 2
b. 2.7
d. 1.5
A certain buffer solution contains equal concentration of X- and HX. Ka for HX is 10-^8. The pH of buffer
is
a. 3
b. 8 ®
c. 11
d. 14
a. pH of solution decreases
b. [H+] decreases
c. [OH-] increases
d. [CH3COO-] increases ®
NaOH will give OH- ions which will combine with H+ ions from CH3COOH and form water. CH3COO- will
left.
Strength of an acid is directly related to
a. Ka ®
b. pKa
c. pH
d. Kw
a. 9
b. 6
c. 2
d. - 2 ®
Lower the pH, stronger will be the acid. Acid have negative values of pH
a. Strong acid
b. Weak acid ®
c. Moderately acid
d. Unpredictable
pH of 0.1M solution of weak acid is 3. The value of ionization constant ka of acid is:
a. 3 × 10-¹
b. 1 × 10-³
c. 0.01 × 10-³ ®
d. 1 × 10-^7
Ka = [H+]²/C = [1 × 10-³]²/0.1 = 1 × 10-^5
The pKb value for aqueous ammonia at 25°C is 4.8. What is correct pKa value for ammonium ions at this
temperature?
a. - 4.8
b. 4.8
c. 9.2 ®
d. 2.2
pKa + pKb = 14
If the difference, of pKa values of the two acids is two, then acid with smaller pKa is
REACTION KINETIC
In a reaction 2A ---> products, the concentration of A decreases from 0.5M to 0.38M in 10 mints. What is
the rate of reaction during this interval?
a. 0.012 M/s
b. 0.024 M/s
c. 0.002 M/s
d. 0.0002 M/s
The rate law for the reaction A + B -----> Product is given by an expression [A][B]. If concentration of B
is increased from 0.1mol to 0.3 mol, keeping the value of A at 0.1 mol, the rate constant will be
a. 3k
b. k/3
c. 9k
d. k ®
a. Increasing temperature ®
b. Decreasing temperature
c. Increasing conc. of O2
d. Increasing conc. of NO
A) concentration
B) temperature ®
C) catalyst
D) Surface area
If the temperature of the reaction is increased from 0°C to 50°C how many times rate will increase?
(A) 5 times
(B) 2 times
(C) 10 times
(D) 32 times ®
Rate of reaction is doubled for 10°C or 10k rise in temperature. For 50k rise in temperature rate of
reaction will be increased by 32 times
At 290 K velocity constant of a reaction was found to be 3.2 × 10-³. At 300 K, it will be
a. 1.6 × 10-³
b. 3.2 × 10-⁴
c. 6.4 × 10-³ ®
d. 3.2 × 10-²
A chemical reaction was carried out at 300k and 280k. The rate constants were found to be K1 and K2
respectively then
a. K2 = 4 K1
b. K2 = 2 K1
c. K2 = 0.25 K1
d. K2 = 0.5 K1
Rate constant double for 10°C or 10k rise in temperature. For 20k rate constant will be 4K K1 = 4
K2 or K2 = 0.25 K1
Rate constant for a reaction H2 + I2 ----> 2HI is 49 then rate constant for 2HI ----> H2 + I2 is
a. 49
b. 1/49 ®
c. 21
d. 63
Velocity constant or rate constant is equal to rate of reaction when concentration of reactants are
a. 0
b. 1 ®
c. 2
d. 3
a. 100 mints
b. 200 mints
c. 346 mints
d. 400 mints
The half life of ist order reaction is 69.35 sec. The value of rate constant of reaction is
a. 1 s-¹
b. 0.1 s-¹
c. 0.01 s-¹
d. 0.001 s-¹
a. Zero order ®
b. First order
c. Second order
d. Third order
For the reaction H2 + Cl2 ----hv---> 2HCl taking place in water, the order of reaction
a. 0
b. 1
c. 2
d. 3
Photochemical reaction between H2 and Cl2 is a zero order reaction. However, the rate is influenced by
the intensity of sunlight.
The rate of photochemical reaction is independent of the concentration, therefore it is zero order
reaction
The plot of concentration of reactants vs time for a reaction is straight line with negative slop. The
reaction follows a rate equation
a. Zero order ®
b. Ist order
c. 2nd order
d. 3rd order
If initial concentration is doubled, the time for half reaction is also doubled. The order of reaction is ...
(a) First
(b) Second
(c) Third
(d) Zero ®
If ‘a’ is the initial concentration of the reactant, the time taken for completion of the reaction, itif is of
zero order, will be
a. k/2a
b. a/2k
c. a/k
d. k/a
For zero order reaction, K= x/t . if x=a (complete reactant to react); t= a/k
b. mol s-¹
c. dm³ s-¹
a. M/s ®
b. s/M
c. M s
d. s-¹
If the half time for a particular reaction is found to be constant and independent of the initial
concentration of the reactants then reaction is of ...
(a) 1 ®
(b) 2
(c) 3
(d) 0
a. Zero order
b. First order ®
c. Second order
d. Third order
a. Zero
b. First ®
c. Second
d. Third
The reaction L ---> M started with 10g L. After 30 and 90 mints 5g and 1.25g of L respectively are left.
The order of reaction
a. 1 ®
b. 2
c. 3
d. 0
After 30 mint amount is reduced from 10g to 5g. its mean half life is 30 mint. In 90 mints amount is
reduced to 1/8 i.e 1/2ⁿ n = 3.
The rate of ist order reaction is 1.5 × 10-² mol L-¹ s-¹ at 0.5 M concentration of reactant. The half life of
reaction is
a. 0.383 min
b. 23.1 min
c. 8.73 min
d. 7.53 min
a. sec-¹ ®
b. mol/dm³
Rate = k[A]²[B] for the reaction 2A + B ----> Product and A is present in large excess, then order of
reaction is
a. 1 ®
b. 2
c. 3
d. 4
If a reactant is in excess it means it is not a limiting reantant. Rate of reaction depends upon limiting
reactant
a. First ®
b. Second
c. Third
d. Zero
a. Zero order
b. Ist order
c. Pseudounimolecular ®
d. 4th order
The rate law, for the reaction Sucrose + Water ---(H+)---> Glucose + Fructose
a. R = k [Sucrose][Water]
b. R = k [Sucrose][Water]°
c. R = k [Sucrose]½[water]½
d. R = k [Sucrose]°[Water]
It is pueudo first order reaction because water is non limiting reactant i.e present in abundance. Plz
read the topic "Method of large excess" if u have any confusion
a. Zero
b. First ®
c. Second
d. Third
a. 1.5 ®
b. 0
c. 1
d. 2
a. Zero
b. First
c. Second ®
d. Third
Half life of reaction becomes half when initial concentrations of reactants are made double. The order of
reaction will be
a. First
b. Second ®
c. Third
d. Zero
t½ = 1/ka Half life and initial concentration are inversly related to each other
The rate of reaction between two reactants A and B decreases by a factor of 4. If the conc. of reactant B
is doubled, the order of reaction with respect to reactant B
a. - 1
b. - 2
c. 1
d. 2
b. 1 ®
c. 2
d. 1.5
a. First order in A
b. Second order in B
The rate expression of a reaction is Rate = k[A]²[B]². What becomes the rate of reaction kf A and B
concentrations are doubled?
a. Doubled
d. Not affected
From given equation NO2 + CO -----> CO2 +NO Which reactants are present in order of equation?
a. NO2 + NO2 ®
b. NO2 + CO
c. NO + CO2
d. NO3 + NO
See textbook
b. Ist order
c. 2nd order
d. 3rd order ®
Half life a reaction is found to be inversly proportional to cube of its initial concentration. The order of
reaction is
a. 2
b. 3
c. 4 ®
d. 5
a. R = k[A]²[B]
b. R = k[A][B] ®
c. R = k[A]²
d. R = k[A][C]
The rate constant of reaction is 3 × 10-³ bar-¹ sec-¹. The order of reaction is ...
(a) 1
(b) 2
(c) 3
(d) 0
K = rate/[R]ⁿ -----> bar s-¹/[bar]²ⁿ = bar-¹ s-¹
In one reaction concentration of reaction A is increased by 16 times, the rate increases only two times.
The order of the reaction would be ...
(a) 2
(b) 4
(c) ½
(d) ¼ ®
If the rate of decay of radio-active isotope decreases from 200 cpm to 25 cpm after 24 hours. What is its
half life:
(A) 3 hours
(B) 4 hours
(C) 6 hours
(D) 8 hours ®
200 ---> 100 ---> 50 ---> 25 its mean 3 half lifes have been passed.
Half life = given period/number of half lifes = 24/3 = 8 hours
For a reaction A+2B ----> C the amount of C forned by starting reaction with 5 moles of A and 8 moles of
B
a. 4 ®
b. 5
c. 8
d. 16
a. Increases
b. Decreases
c. Remain same ®
Only the rate of reaction increases but order of reaction remains same
a. Enthalpy
b. Entropy
c. Nature of reactants
d. Energy of activation ®
a. Al2O3 ®
b. Te
c. Fe
d. Ni
c) It activates equilibrium
The main purpose of using a catalyst is only to increase the rate of achieving the equilibrium state in
case of slow reaction. Other than that it will not initiate or involve in the reaction.
a) Potassium nitrate
b) Aluminium nitrate
c) Aluminium oxide
d) Chlorine
Aluminium oxide is known for its sophisticated properties and is mainly used in the process of corrosion
preventing it absorbs moisture and has high retentivity and hence is used as a catalytic poison.
a) Zinc
b) Chlorine
c) Platinum
d) Water
Since nitrogen and noble metals components have the same equilibrium valencies, we can see that one
will promote the other and vice versa. Thus nitrogen molecule is the best for platinum molecules.
Which of the following is used as a catalyst for the following reaction? H2O2 ⟶
2H2O + O2
a) Chlorine
b) Bromine
c) Platinum
d) Noble solutions
Since oxygen and noble metals components have same equilibrium valencies, we can see that one will
promote the other and vice versa. Thus oxygen molecule is the best for platinum molecules.
Which of the following is used as a catalyst for the following reaction? 2SO2 +
O2 ⟶2SO3
a) Chlorine
b) Nitrous oxide
c) Sulphur di oxide
d) Potassium chloride
Since sulphur and nitrogen components have the same equilibrium valencies, we can see that one will
promote the other and vice versa. Thus nitrogen molecule is the best for sulphur molecules.
Which of the following is used as a catalytic poison for the same reaction:
SO2 + O2 ⟶2SO3
a) Platinum
b) Bromine
c) Magnesium
d) Silver
Though nitrogen is used as a promoter, we can see that platinum reduces its activity and hence
decreases the rate of reaction of equilibrium in the above reaction.
Process in which catalyst has a different phase to a reaction mixture, this process is known as
a. homogeneous catalysis
b. heterogeneous catalysis ®
c. hypergeneous catalyst
d. hypogenous catalyst
a) Enzyme catalysis
c) Haber’s process
Enzyme catalysis is an example of homogeneous catalysis. All the other options are not examples of
homogeneous catalysis.
Changes in oxidation number of ions which are involved in catalysis are done in
a. homogeneous catalysis ®
b. heterogeneous catalysis
c. hypergeneous catalyst
d. hypogenous catalyst
Homogeneous catalysis by soluble transition metal complexes offers many advantages over
heterogeneous catalysis, such as milder reaction conditions, higher activities and selectivities, and better
control of operating conditions. Such superior performance arises from the ability of transition metals to
complex with a wide variety of ligands in a number of geometries and to easily change from one
oxidation state to another
When temp. increases, the activation emergy of a reaction..?
a. increases
b. decreases
Activation energy can't be altered by temperature. Catalysts are molecules that speed up reactions.
Catalysts reduce the activation energy of reactions so that more successful reactions can occur without
increasing the temperature.
Consider an endothermic reaction, X....... >Y with the activation energies Eb and Ef for backward and
forward reaction respectively. In general :
a. Eb > Ef
b. Eb < Ef
c. Eb = Ef
When the energy of products is lesser than reactants, the reaction is exothermic. Energy of activation of
forward reaction is less than backward reaction for an exothermic reaction. • When the
energy of products is higher than reactants, the reaction is endothermic. Energy of activation for
backward reaction is less than forward reaction for an endothermic reaction
For and endothermic reaction, where ∆H represents enthalpy of reaction in KJ/mol, the minimum value
for energy of activation will be
a. Less than ∆H
b. More than ∆H ®
c. Equao to ∆H
d. Zero
For an exothermic reaction an activation energy of 70 KJ mole-¹ and the enthalpy change of reaction is
30 KJ mole-¹. The activation energy for the reverse reaction is ...
(a) 70 KJ mole-¹
(b) 30 KJ mole-¹
(c) 40 KJ mole-¹
For an endothermic reaction A ---> B. An activation energy of 15 Kcal mole-¹ and the enthalpy change of
reaction is 5 Kcal mole-¹ . The activation energy for the reaction B ---> A is
(d) zero
The activation energy of a reaction A+B ---> C+D+38 kcal is 20 kcal. What would be the activation energy
of the reaction C+D ---> A+B
a. 20 kcal
b. - 20 kcal
c. 18 kcal
d. 58 kacl ®
Energy is released is this reaction i.e 38 kcal so take ∆H is - ve because reaction is exothermic ∆H = Ef
- Er ----> - 38 = 20 - Er ----> Er = 58 kcal
With increase of 10°C temperature, the rate of reaction becomes doubled.This increase in rate of
reaction is due to
a. Temperature
b. Nature of reactants ®
d. Concentration of reactants
Substances differ markedly in the rates at which they undergo chemical change. The differences in
reactivity between reactions may be attributed to the different structures of the materials involved; for
example, whether the substances are in solution or in the solid state matters. Another factor has to do
with the relative bond strengths within the molecules of the reactants. For example, a reaction between
molecules with atoms that are bonded by strong covalent bonds will take place at a slower rate than
would a reaction between molecules with atoms that are bonded by weak covalent bonds. This is due to
the fact that it takes more energy to break the bonds of the strongly bonded molecules.
a. Graphical method ®
c. Spectrometry
d. Dilatometric method
CHEMISTRY PART 2
PERIODS
Which of the following decreases along the period?
a. Atomic radius ®
b. Shielding effect
c. Ionization energy
d. electron affinity
a. Mg > Al
b. Lu > Ce
c. Ba > Mg ®
d. Cl > I
Size decreases along the period while increases down the groups. Mg > Ca > Sr > Ba > Ra
a. Atomic radius ®
b. Atomic mass
c. Ionization energy
d. Electronegetivity
a. Na
b. He
c. Cl
d. Fr ®
a. Al
b. Si
c. P
d. Mg ®
Atomic radius decreases along the period. Mg > Al > Si > P > S > Cl
Ionic radius of Na :
a. 186pm
b. 95pm
c. 99pm
d. 181pm
Atomic radius and ionic radius of Na are 186 and 95pm respectively. Atomic radius and ionic radius of Cl
are 99pm and 181pm
a. X
b. X+
c. X- ®
Greater the negative charge, greater the size. Greater the positive charge lesser is the size
Which species respresented by the following formula has largest radius
a. P-³ ®
b. Cl-
c. Ar
d. K+
Greater the negative charge, greater the size. Greater the positive charge lesser is the size
a. H
b. He
c. Li+
d. Be+² ®
a. N-³ ®
b. F-¹
c. Al+³
d. Na+¹
Greater the negative charge, greater the size. Greater the positive charge lesser is the size
a. O²¯
b. C⁴¯
c. F¯ ®
d. N³¯
Greater the negative charge, greater the size. Greater the positive charge lesser is the size
a. Al ®
b. Al+¹
c. Al+²
d. Al+³
a. K+
b. Na+
c. Li+
d. Be+² ®
a. Ca and Be
b. Mg and Al ®
c. O2 and H2
d. Na and O2
Diagnol relationship
Al is diagonally related to
a. Li
b. C
c. B
d. Be ®
a. +1
b. - 1
c. +4 ®
d. - 4
a. +3 ®
b. +5
c. +3 and +5
d. +6
a. +3
b. +5
c. +3 and +5 ®
d. +6
+5 oxidation state w.r.t number of electrons in valence shell. +3 oxidation state w.r.t number of
vacancies
a. B
b. N
c. S
d. Mn ®
a. P, S
b. N, Ge
c. N, P ®
d. P, O
d. Maximum O.S is +7 ®
a. +3 ®
b. +5
c. +7
d. +1
It is the steady decrease in size of atoms and ions of rare earth elements with increasing atomic number
from lanthanum (57) through luteium (71)
Which one of the following elements has non variable oxidation state?
a. Be ®
b. Br
c. Cl
d. N
b. Sn
c. C
d. Si
C and Si are poor conductors. Tin and lead are lead good conductors. Tin has greater conductivity than
lead
a. Cu, Ag, Hg
b. Cu, Au, Ag ®
c. Ni, Co, Zn
d. Ni, Co, Pt
Atomic number for four elements are 14, 17, 19 and 20. Which of the following element has lowest
melting point?
Number of electrons in valence shell indicates group to which an element belongs 14 >>
IV group | 17 >> VII group | 19 >> I A group | 20 >> II A group Elements of IV
group have very high melting points because they have maximum number of binding electrons.
Elements of IA group have low melting points. Elements of VII and VIII have very low melting points.
Trend of M.P in groups. IA < IIA < IIIA < IV > VI > VII > VIII Trend of melting point in given
options. 14 > 20 > 19 > 17
b. S
c. Cl
d. Ar
Trend of M.P in groups. IA < IIA < IIIA < IV > VI > VII > VIII. P < S > Cl > Ar
a. H ®
b. He
c. Cl
d. Ar
Elements of IV group have very high melting points because they have maximum number of binding
electrons. Elements of IA group have low melting points. Elements of VII and VIII have very low melting
points. Trend of M.P in groups. IA < IIA < IIIA < IV > VI > VII > VIII . Melting points decreases down the
group. H > He > Cl > Ar
a. C
b. Si
c. Ca
d. Mg
Elements of 4th group (C, Si) have very high melting points. Melting point decreases down the group so
Ca would have lowest melting point but this is not true. Due to hexagonal structure of Mg, it has lower
melting point than Ca
a. F2
b. Cl2
c. Br2
d. I2 ®
Usually melting and boiling point decreases down the group but in VII group, melting and boiling point
increases down the group due to increase in polarizability
a. AlF3 ®
b. AlCl3
c. AlBr3
d. AlI3
Greater the electronegetivity difference greater the ionic character and greater will be the melting point.
AlF3 is purely ionic compound while AlI3 is predominantly covalent
a. AlF3
b. AlCl3
c. AlBr3
d. AlI3 ®
Greater the electronegetivity difference greater the ionic character and greater will be the melting point.
AlF3 is purely ionic compound while AlI3 is predominantly covalent. Covalent character increases as the
size of halide ion increases
a. C ®
b. O
c. H
d. N
Because it sublimize
Hydrides of forth period show greater boiling point than those of third period due to
a. Hydrogen bonding
b. Greater size ®
c. Low electronegetivity
The energy released by gaseous ions when dissolving in water is called enthalpy change of
a. solution
b. hydration ®
c. atomization
d. electron affinity
a. Increases ®
b. Decreases
c. Remain same
d. Variable
a. Na+
b. F-
c. Al+³ ®
d. Sr+²
a. Cs+²
b. Mg+² ®
c. Ba+²
d. Na+
Greater the positive charge, greater the hydration energy. IF more than 1 species have same positive
charge then check their size. Smaller the size, greater will be the hydration energy
a. Li+
b. Na+
c. K+ ®
Greater the positive charge, greater the hydration energy. IF more than 1 species have same positive
charge then check their size. Smaller the size, greater will be the hydration energy
Ionization energy does not depend upon one of the following factor
A) atomic number
B) shielding effect
C) nuclear force
D) mass number ®
a. s ®
b. p
c. d
d. f
s electrons are strongly bounded to nucleus so Large amount of energy is required for removal of
electron
a. Alkali metals ®
c. Halogens
d. Inert gases
Lower the no. of valence electrons lower is the value of ionization potential
a. Li ®
b. He
c. H
d. Fe
a. Metals ®
b. Non metals
c. Semi metals
d. Metalloids
a. Nobal gases ®
b. Transition elements
c. Platinum metal
a. B
b. K
c. Na
d. Kr ®
a. B
b. Li
c. Ne ® noble gas
d. F
b. H
c. N
d. B
the first ionization energy of beryllium is greater than that of boron because beryllium has a stable
complete electronic configuration (1s², 2s²) so it requires more energy to remove the first electron from
it. Electronic configuration of boron is 1s², 2s², 2p¹ Ionization energies of
III-A and VI-A show abnormal trend
a. Li ----> Li+
b. Cu ----> Cu+
c. Br ----> Br-
d. I ----> I-
Ionization energy increases from left to right in period. Ionization energies of III-A [Al] and VI-A show
abnormal trend
a. 1
b. 2
c. 4 ®
d. 6
a. P ®
b. Si
c. Mg
d. Al
P belongs to group having nitrogen means P has Stable half filled configuration. Further Ionization
energy increases from left to right in period.
Which ionization potential in the following equations involve greatest amount of energy?
K on losing electron gains electronic configuration of Argon(noble gas) Electron is to be removed from
stable configuration. C+² = Be. Now of course there is no comparison of ionization energy of noble gases
with others. When ever it is asked about ionization energy, and you see that noble gas is given in the
option, just mark it without any hesitation.
a. 419 kj/mol ®
b. -349 kj/mol
c. 721 kj/mol
d. 1870 kj/mol
a. Na
b. Mg ®
c. Al
d. K
Ionization energy increases from left to right in period. Ionization energies of III-A [Al] and VI-A show
abnormal trend.
First four ionization potential values of an element are 191, 578, 872 and 5962 kcal. The number of
valence electrons in element are:
a. 1
b. 2
c. 3 ®
d. 4
Larger gap between 3rd and 4th ionization energies. Since 4th I.E is very high. Thus electron is to be
removed from stable configuration
a. N
b. O ®
c. F
d. Ne
Ionization energy increases from left to right in period. Ionization energies of III-A and VI-A [O] show
abnormal trend.
a. B ®
b. C
c. N
d. O
a. N ®
b. O
c. S
d. P
Ionization energy increases from left to right in period. Ionization energies of III-A and VI-A [O] show
abnormal trend.
a. C > N > O
b. C < N < O
c. C < N > O ®
d. N > O > C
Ionization energy increases from left to right in period. Ionization energies of III-A and VI-A [O] show
abnormal trend
a. C
b. N
c. O ®
d. F
After removal of 1 electron, oxygen attains configuration of nitrogen (half filled p orbital)
a. Ionization energy ®
b. Electron affinity
c. Electronegetivity
d. Shielding effect
a. 2
b. 8
c. 10 ®
d. 7
a. Ionization energy
b. Electron affinity ®
c. Electronegetivity
d. SHielding effect
a. 1s² ®
Stable configuration (douplet is complete). Ionization energy for s > p > d > f. Nearer the subshell to
nucleus experiences greater nuclear force and hence require greater amount of energy for removal of
electron
a. He ®
b. Ne
c. Ar
d. Na
Nobles gases have highest ionization energy. Ionization energy decreases down the group
Electron affinity for noble gases
a. Zero ®
b. High
c. Positive
d. Negative
Stable electronic configuration and nucleus does not show attraction for extra electron
a. Nuclear charge
b. Atomic number
c. Atomic size
a. Alkali metals ®
c. Halogens
d. Oxygen family
Atomic radius decreases from left to right due to increase in nuclear charge. Thus electron affinity
increases from left to right. Thats why alkali metals have loewst and halogens have highest electron
affinity
E.A increases from Left to right but elements belong to V-A group[N] has low electron affinity generally
considered zero because they have stable configuration(half filled p orbital) so they do not gain electron
because if they do so them become unstale. VI > IV > III > V
a. Oxygen
b. Nitrogen ®
c. Carbon
d. Boron
a. B
b. N
c. Be
d. Cl ®
Electron affinities of halogens are F = 322, Cl = 349, Br = 324 and I = 295kj/mol. The higher value for Cl
as compared to F is :
b. Smaller electronegativity of F
Smaller radius of F and its high charge density makes its Electron affinity low. Size of fluorine atom is
very small as compared to chlorine atom and due to its small size there are strong inner repulsions
among valence electrons and so the outer electron doesnot feel the attraction from the nucleus. So
electron affinity of fluorine is less than that of chlorine.
In which of the following pairs of element, ist element of the pair has greater electron affinity
a. B, Al
b. N, P
c. S, O ®
d. F, Cl
As we move down a group from top to bottom electron Affinity becomes less negative because size of
atom increases . Electron Affinity for third period elements i.e ( Al, P , S , Cl ) their Electron Affinity is
more negative than the second period elements i.e (B, N , O, F ) , This due to smaller size of the atoms of
second period elements which produce larger electron repulsion for addition of electron
a. F
b. Cl ®
c. Br
d. I
a. Na
b. Mg
c. Al
d. Si ®
Electron affinity increases across periods. but elements belong to V-A[Si] group has low electron affinity
generally considered zero because they have stable configuration(half filled p orbital) so they do not
gain electron because if they do so them become unstale
Which of the following has highest electron affinity?
a. O
b. O-
c. F-
d. Na
F- is already negatively charged and its octet is complete hence it is neutral, so eliminate that Na is
electropositive instead of accepting it will lose electrons, hence it is no incentive to add electrons,
eliminate this too Now between O and O-,O has the highest affinity towards electrons than O- because
size of O < O¯= F. Due to smaller size of O, there will be greater force of attraction of nucleus. Hence O is
the correct answer.
a. Cl- ®
b. Ar
c. K+
d. Ca+²
All are iso-electronic species. If iso-electronic species are given, see their size. Of course negatively
charged species have greater size. Greater size means less nuclear attraction and hence easier will be
the removal of electron and lower will be the ionization energy.
Number of electrons in valence shell indicates group number of that element. Electron affinity increases
along periods. Option a has configuration of VA group. Option B has configuration of VII A group. Option
C has configuration of VIII A group. Option D has configuration of I A group.
On Pauling scale, which of the following does nit have electronegetivity equal or greater than 3.0
a. Oxygen
b. Nitrogen
c. Bromine ®
d. Chlorine
a. Large size
a. C
b. Mg
c. O ®
d. S
Increases along the period because of high nuclear charge and small size
a. P ®
b. As
c. Bi
d. Sb
a. C ®
b. Si
c. Sn
d. Pb
a. C, N, Si, P
b. N, Si, C, P
c. Si, P, C, N ®
d. P, Si, N, C
N, P belongs to V A group while C, Si belongs to IV A group. Moreever C, N belongs to same period and
Si,P belongs to same peeiod. Electronegetivity decreases down the group. Electronegetivity increases
along the period.
a. BaO
b. Na2O ®
c. As2O3
d. Al2O3
a. MgO
b. BeO ®
c. BaO
d. CaO
Less electripositive elements (Be, Al, Ga, In, Bi) form amphoteric oxides.
a. SO3 ®
b. MgO
c. ZnO
d. Bi2O3
a. MnO
b. Mn2O7 ®
c. MnO2
d. Mn2O3
Oxidation state of metal also affects acid/base character of its oxides. The acidity increases with
increasing oxidation state. MnO < Mn2O3 < MnO2 < Mn2O7
a. MgO
b. SiO2
c. SO3
d. Cl2O7 ®
In a given period, oxides progess from stongly basic through weakly basic, amphoteric and weakly acidic
to strongly acidic
Which of the following oxides have low basicity?
a. BeO
b. MgO
c. CaO
d. BaO ®
Basicity of metal oxides increases down the group while acidity increases along the period
a. Decreases ®
b. Increases
c. Remain same
The order in which of the following oxides are arranged according to decreasing basic nature is:
Along period, acidic character increases while Basic or metallic character decreases
a. Ba(OH)2
b. Mg(OH)2
c. Ca(OH)2
d. Ba(OH)2 ®
Halogen atoms in which halides act as bridge between two atoms of other elements :
a. Covalent halides
b. Ionic halides
c. Polymeric halides ®
Structure of AlCl3 is polymeric in which halogen (Cl) atom acts as bridge btween two metal atoms(Al)
a. Be ®
b. Na
c. Ba
d. P
Strongly electropositive elements (IA and IIA except Be) have higher electrienagtivity difference so they
form ionic halides. Less electropositive elements like Be, Ga, Al form polymeric halides. Less
electropositive elements of IV A, V A and VI A having less electronegetivity difference with halogens
form covalent halides. Na and Ba form ionic halides while P form covalent halide
a. ZnH2
b. InH2
c. SiH4 ®
d. CdH2
Only MgH2, ZnH2, CdH2, TnH3 and TiH3 are Intermediate Hydrides. SiH4 is a covalent hydride
Halides having highest lattice energy are:
a. Iodides
b. Bromides
c. Chlorides
d. Flourides ®
Due to smaller size of F- ion, ionic flouides are more stable. So they have high lattice energy
Which of the following statements is not correct for an element having electronic configuration 1s2, 2s2,
2p6, 3s1
a. It is a monovalent electropositive
c. It is non metal ®
GROUPS
The electronic configuration of an element is 1s2, 2s2, 2p6, 3s2, 3p3. What is the atomic number of the
element which is just below the above element in periodic table?
a. 31
b. 33
c. 34
d. 41
For atomic number 33, number of electrons in valence shell are 5. Its mean it belongs to same period to
which element whose configuration is given in questions belongs
Which of the following pair has same number of electrons in valence shell?
a. N, O
b. Na, Ca
c. As, Bi ®
d. Pb, Sb
c. Atomicity
d. Number of shells
a. Chemical reactivity
a. MgO, Mg3N2 ®
b. MgO
c. Mg(OH) 2, NH3
d. Mg3N2, NH3
a. BaO
b. Ba2O
c. Ba2O3
d. BaO2 ®
The alkaline earth metals burn in oxygen to form normal oxides except barium which form peroxides
a. Low pressure, Pt
b. High pressure, Pt
a. MgO, Mg3N2
b. MgO
c. Mg(OH)2, NH3
d. Mg3N2 ®
a. MgO ®
b. Mg(OH)2
c. Mg3O2
d. Mg does not react with water
Mg reacts slowly with boiling water and quite with steam to produce oxide and H2
a. BaO
b. Ba(OH)2 ®
c. Ba3O2
a. Low temperature
b. High temperature
a. BeO ®
b. BaO
c. CaO
d. SrO
BeO and MgO are insoluble while CaO, SrO, BaO are soluble.
Which of the following oxides can react with both acids and bases?
a. BeO ®
b. BaO
c. CaO
d. SrO
a. BeO
b. BaO ®
c. CaO
d. SrO
a. NaOH
b. KOH
c. CsOH
d. Mg(OH)2
All alkali metal hydroxides are stable to heat except LiOH whike alkaline earth metal hydroxides like
Mg(OH)2 and Ca(OH)2 decompose on heating
Which of the following carbonates of alkaline earth metals are least soluble in water?
a. BeCO3
b. MgCO3
c. CaCO3
d. BaCO3 ®
a. BeCO3 ®
b. MgCO3
c. CaCO3
d. BaCO3
Ease of decomposition decreases down the group. The ease of decomposition can be related to the size
of metal ion, smaller the ion, the more is the lattice energy of the resulting oxide and hence higher the
stability of the product
d. Metallic oxide + O2
a. Only oxygen
c. Only hydrogen
Which of the following sulphates of alkaline earth metals are insoluble in water?
a. BeSO4
b. MgSO4
c. CaSO4
d. BaSO4 ®
BeSO4 and MgSO4 are fairly soluble in water. CaSO4 is slightly soluble in water. SrSO4 and BaSO4 are
almost insoluble
Which of the following pairs of compounds of alkaline earth metals have opposite solubility trend?
Solubility of carbonates, nitrates and sulphates decreases down the group. Solubility of oxides and
hydroxides increases down the group.
(A) Fluorine
(B) Chlorine
(C) Iodine
(D) Astatine ®
Only halogen that exists as liquid is bromine. The colour of bromine is:
a. Pale yellow
b. Greenish yellow
c. Redish brown ®
d. Grayish black
a. F2
b. Cl2
c. Br2 ®
d. I2
a. Fluorine ®
b. Chlorine
c. Bromine
d. Iodine
Flourine has highest ionization energy and electronegativity. Chlorine has greater electron affinity and
bond energy
a. F-F
b. Cl-Cl ®
c. Br-Br
d. I-I
a. Fluorine
b. Chlorine
c. Bromine
d. Iodine ®
a. Ionization energy ®
b. Hydration energy
c. Energy of dissociation
d. Electron affinity
Oxidizing power of halogens depends upon Hydration energy, Energy of dissociation, Electron affinity
and heat of vapourization(for Br2, I2)
Which of the following reactions is not feasible according to the electrochemical series?
Flourine is the strongest Oxidizing agent. It can oxidize all other halogens. Cl can oxidize Br and I. Iodine
is a weak Oxidizing agent it cannot oxidize other halogens
a. F
b. Cl ®
c. Br
d. I
a. F
b. Cl
c. Br
d. I ®
a. NaF
b. NaCl
c. NaI
d. All of these
A substance X when treated with conc. Sulphuric acid liberates a gas which turns starch paper blue. The
substance X is
a. NaI ®
b. NaCl
c. NaF
d. NaNO3
a. Na2SO4 + HF ®
b. Na2SO4 + F2
d. Na2SO4 + SO2 + F2
NaF and NaCl produce same products(Na2SO4+Acid) while NaBr and NaI produce same
products(Na2SO4+Halogen)
a. NaCl ®
b. MnO2
c. KMnO4
d. K2Cr2O7
b. Pure oxygen
c. Moisture ®
d. Dry air
a. HF ®
b. HCl
c. HBr
d. HI
a. H-F ®
b. H-Cl
c. H-Br
d. H-I
a. Sodium hypochlorite ®
b. Sodium chlorite
c. Sodium chlorate
d. Sodium perchlorate
b. Reduction reaction
c. Disproportionation reaction ®
d. Decomposition reaction
a. F
b. Cl ®
c. Br
d. I
a. F
b. Cl
c. Br ®
d. I
a. 2-Bromo-2-chloro-1,1,1 trifluoroethane ®
b. 2-Chloro-2-bromo-1,1,1 triflouroethane
c. 2-bromo-2Iodo-1,1,1 triflouroethane
d. 2-Bromo-2-chloro triflouroethane
Monomer of Teflon is :
a. - CH2-CH2-
b. - CF2-CF2- ®
c. - CCl2-CCl2-
d. - CBr2-CBr2-
-------- is a valuable plastic which resists the action of oxidants, acids and alkalies
a. Freon
b. Teflon ®
c. PVC
d. Pyrene
a. Freon
b. Teflon
c. PVC
d. Pyrene ®
Feron is used in refrigeratnts and aerosol propellants. Teflon is a valuable plastic which resists the action
of oxidants, acids and alkalies. PVC is a plastic. Pyrene is a trade name of CCl4. It is used a solvent.
Pyrene is also used in fire extinguisher.
a. F
b. Cl
c. Br ®
d. I
Tincture of iodine is a :
b. Solution of I2 in aqueous KI ®
c. Germicide
a. Feron
b. Teflon ®
c. Argon
d. Krypton
a. Formation of PVC
b. Photography ®
a. Ni
b. Fe
c. Mn
d. Cr
Number of unpaired electrons in ground state in elements of period increases from Sc to Cr then
decreases to Zn. Si (1), Ti (2), V (3), Cr (6), Mn (5), Fe (4), Co (3), Ni (2), Cu (1), Zn (0)
a. Cr+³ ®
b. Sc+³
c. Al+³
d. Mn+²
Sc+³ (0), Ti+³ (1), V+³ (2), Cr+³ (3), Mn+³ (4), Mn+² (5), Fe+³ (5), Fe+² (4), Co+² (3), Ni+² (2), Cu+² (1), Zn+²
(0)
b. Ionization
d. Loss of s electron
a. Ti+⁴ ®
b. Cr+³
c. Mn+²
d. Cu+²
a. Ti+³, Cu+²
b. Co+² , Fe+³
c. Sc+³ , Zn+² ®
d. Ni+², V+³
Because they have zero unpaired electrons. Sc+³ (0), Ti+³ (1), V+³ (2), Cr+³ (3), Mn+³ (4), Mn+² (5), Fe+³
(5), Fe+² (4), Co+² (3), Ni+² (2), Cu+² (1), Zn+² (0)
a. Mg+²
b. Ti+³
c. V+³
d. Fe+² ®
Sc+³ (0), Ti+³ (1), V+³ (2), Cr+³ (3), Mn+³ (4), Mn+² (5), Fe+³ (5), Fe+² (4), Co+² (3), Ni+² (2), Cu+² (1), Zn+²
(0)
a. p electrons in Ne
b. s electrons in Mg
c. d electrons in Fe
d. p electrons in Cl¯ ®
Fe+² = 1s2, 2s2, 2s6, 3s2, 3p6, 3d6 Cl¯ = 1s2, 2s2, 2p6, 3s2, 3p6 Mg =
1s2, 2s2, 2p6, 3s2 Ne = 1s2, 2s2, 2p6
An element is in M+³ form. Its electronic configuration is [Ar] 3d¹, the ion is
a. Ti+³
b. Ti+⁴
c. Ca+²
d. Sc+
a. Electronic configuration
b. Oxidation state ®
c. Ionization energy
d. Formation of complexes
No. of electron pairs accepted by the central atom in a transition metal complex is called:
(D) Chelate
-------- indicates number of dative bond formed by metal ion or atom
a. Nature of chelates
c. Coordination number ®
d. Oxidation number
a. 0
b. 2
b. 4
d. 6
(A) Zero
(B) One
(C) Two ®
(D) Three
(A) 2
(B) 4
(C) 6 ®
(D) Zero
Co-ordination number of Pt in K2[Pt Cl6]
a. Zero
b. 4
c. 6 ®
d. 2
(B) Ligand
(A) Ammine
(B) Carboxyl
(C) Oxalato ®
(D) Acetato
(A) NH3
(B) H2O
(C) CO
(D) CN–
a. 4 and 6 ®
b. 2 and 4
c. 3 and 5
d. 0 and 1
You can say 2 is also common. But 6 is very common. From given options, 4 and 6 is the better choice
a. [Mn Cl4]-²
b. [Cu (NH3)4]+² ®
c. [Fe(CO)5]
d. [Co (NH3)6]+³
Complexes with coordination number 4 may have either tetrahedral or square planar geometry.
Complexes with coordination number 6 have octahedral geometry. For complexes having coordination
number 4: If ligand is
strong, and the metal ions are the following ones then the geometry is square planar.Co2+, Ni3+, Ni2+,
Cu2+. Strong ligands are mostly those
ligands whose election pair is on a C or N atom. Ex: CH3-, CN-, NH3, etc.
a. Tetrahedral ®
b. Octahedral
c. Square pyramidal
d. Linear
Complexes with coordination number 4 may have either tetrahedral or square planar geometry
[CoCl6]¯³ may be geometry:
a. Tetrahedral ®
b. Octahedral
c. Square pyramidal
d. Square planar
Complexes with coordination number 4 may have either tetrahedral or square planar geometry.
Complexes with coordination number 6 have octahedral geometry
(A) Tetrahedral
(B) Octahedral
(D) Tetragonal
(A) Tetrahedral ®
(B) Octahedral
(D) Tetragonal
COMPOUNDS OF NITROGEN AND SULPHUR
Which element is essential component of most of the fertilizers?
(a) C
(b) N ®
(c) P
(d) K
Nitrogen is part of the chlorophyll molecule, which gives plants their green color and is involved in
creating food for the plant through photosynthesis. Thus, Nitrogen enhances yield and quality of plants
(a) Ammonia ®
(b) Urea
a. Ammonia ®
b. Ammonium sulphate
c. Ammonium nitrate
d. Ammonium chloride
Which of the following nitrogenous fertilizer do not make soil acidic?
a. Potassium nitrate ®
b. Ammonia
c. Ammonium sulphate
Potassium nitrate, Sodium nitrate and calcium nitrate do not make soil acidic while all others
nitrogenous fertilizes make soil acidic
a. Ammonia
b. Potassium nitrate
c. Urea ®
d. Calcium nitrate
a. Ammonia
b. Potassium nitrate
c. Urea ®
d. Calcium nitrate
a. 1:2 ®
b. 2:1
c. 1:4
d 1:3
a. Oxidation reaction
b. Reduction reaction
c. Decomposition reaction
d. Neutralization reaction ®
a. Acidic
b. Basic
c. Amphoteric
d. Hygroscopic ®
(a) Cotton
(b) Wheat
(c) Sugarcane
b. It is hygroscopic in nature
d. it is organic in nature
Which of the following is the major source of acid deposition in atmosphere?
a. CO2
b. NO
c. SO2 ®
d. CO
Which of the following gases have pungent ordour and are suffocating?
a. CO
c. NO and NO2
d. Methane
a. Volcanes ®
b. Combustion of coal
c. Transportation
d. Industries
(a) Sulphur
(b) CFCs
(c) Ozone
a. Low temperature
b. High pressure
c. Excess of oxygen ®
d. Pt as a catalyst
Low pressure (2atm), high temperature (400-500°C), Excess of oxygen, Presence of V2O5
a. S + O2 ----> SO2
SO3 is dissolved in 98% H2SO4 to give oleum which is converted into sulphuric acid by mixing water. SO3
is not dissolved in water directly because reaction is highly exothermic.
a. S
b. SO2 ®
c. SO3
d. H2S2O7
In purifying unit, gases after passing through lead pipes are washed by :
a. Spray of water ®
b. Steam
c. Conc. H2SO4
d. Coke
a. Dilute H2SO4
b. Conc. H2SO4 ®
c. Steam
d. Boiling
a. Ferric hydroxide
b. Coke ®
c. Lead
d. Iron
As2O3 is removed in the purifying unit of contact process for the manufacture of H2SO4:
(a) to act as a catalyst
(b) to act as an autocatalyst
In contact chamber, pre-heated gases at 400-500°C are passed through ------ packed with V2O5
a. Lead columns
b. Iron columns ®
c. Platinum columns
d. Copper columns
a. Oxidizing agent
b. Sulphonating agent
c. Dehydrating agent
d. Reducing agent ®
Which products are formed when formic acid is treated with conc. H2SO4?
a. CO2 , H2O
b. CO , H2O ®
c. CO, H2
d. CO2, CO, H2O
a. SO2 ®
b. SO3
c. H2S
d. It cannot oxidize S
a. CO
b. CO2
c. O2
d. NH3 ®
Ammonia cannot be dried by passing over conc. sulphuric acid because ammonia gas reacts chemically
with conc. sulphuric acid to form ammonium sulphate. The actual chemical used for drying ammonia is
Calcim oxide. Hydrogen sulphide gas also
cannot be dried using sulphuric acid as H2S gas is oxidised by sulphuric acid to Sulphur. Therefore, the
H2S gas has chemical action with acid and hence it reacts with it, therefore, cannot be dried using it.
ENVIRONMENTAL CHEMISTRY
Which of the following is a primary pollutant?
a. CO ®
b. Aldehyde
c. PAN
d. H2SO4
a. Nitrogen oxides
b. Hydrocarbons
c. Ozone ®
d. Ammonia
It damages eyes, decreases elasticity of lung tissues, coughing, chest decomfort and aggravates asthama.
It is harmful to the plants. It reduces durability of rubber. It causes fabric dyes to fade
a. Colourless gas
b. Odourless gas
c. Three times Lighter than air
d. Insoluble in water ®
a. Forest fire
b. Volcanic erruption
c. Industrial process
a. 3 days
b. 4 days ®
c. 3 hours
d. 4 hours
a. Nitrogen gas
b. Methane ®
c. Sulphur oxides
d. Nitrogen oxides
a. Ca
b. Al
c. Hg
d. Na ®
The elevated concentration of ----- in water is harmful for fish as it clogs the gills thus causing suffocation
a. S
b. Al ®
c. Pb
d. Hg
In some countries, due to release of ----- by volcanic eruption, there is temporary acid rain
a. SO2
b. SO3
c. HCl ®
d. CO2
a. 320 DU
b. 350 DU ®
c. 290 DU
d. 420 DU
a. Troposphere
b. Mesosphere
c. Stratosphere ®
d. Thermosphere
Ozone act as pollutant when it is present in :
a. Troposphere ®
b. Mesosphere
c. Stratosphere
d. Thermosphere
a. Troposphere
b. Stratosphere ®
c. Mesosphere
d. Thermosphere
a. Oxygen
b. Ozone ®
c. Halogens
d. Neon
a. 1 Lac
b. 10 thousands
c. 2 lac ®
d. 20 thousands
Chlorine atom can destroy 1lac molecules of ozone. Chlorine molecule can destroy 2Lac molecules of
ozone
Peroxyacetyl nitrate is an irritant to human beings and it affects human:
(A) Eyes ®
(B) Nose
(C) Ears
(D) Stomach
MACROMOLECULES
Incorrect statement about addition polymerization?
c. It is ionic in nature ®
d. It requires catalyst
a. PVC
b. Polystyrene
c. Polyester resins ®
d. PVA
(A) Dacron ®
(B) Polyethene
(C) PVA
(D) Nylon
a. C-N
b. C-O ®
c. C-C
d. N-O
Dacron does not have peptide linkage. It has ester linkage. Also known as polyester.
a. C-N ®
b. C-O
c. C-C
d. N-O
a. Hexamethylene diamine ®
b. Adipic acid
c. Terepthalic acid
d. Heptanedioic acid
A polymeric substance that is formed in the liquid state and then hardened to a rigid solid is called
A) Fiber
B) Plastic
C) Varnish
D) Polyamide resin ®
a. Protein ®
b. Nylon
c. Nylon 6,6
d. Urea
(A) Polyester
(C) Nylon-6-6
(D) Polyamide
a. Primary structure
b. Secondary structure ®
c. Tertiary structure
d. Quaternary structure
a. Covalent bond
b. Hydrogen bond ®
c. Peptide bond
a. Sugar + Base ®
b. Sugar + Acid
d. H3PO4 + Nucleotide
The key to the ability of DNA to preserve genetic information and to pass it on from generation to
generation is :
c. Hydrogen bonding
d. Absence of uracil
a. Nucleic acid
b. RNA
d. Chromosomes
a. DNA
b. RNA
c. Nucleic acids ®
d. Purines
a. Uracil
b. Thymine
c. Guanine
d. Cytosine
(A) Cytosine
(B) Thymine ®
(C) Adenine
(D) Guanine
___________________________________________________________________
______
ORGANIC CHEMISTRY
FUNDAMENTAL CONCEPT
a. CO2
b. CO2 + H2O
c. CO + H2O
d. CO + CO2 + H2O
a. CO2
b. CO2 + H2O
c. CO + H2O
d. CO + CO2 + H2O
b. Ethane
c. Propane
d. Butane
4. Which term is used to convert higher alkane into lower alkane / alkene
(A) Pyrolysis
(B) Hydrolysis
(C) Catalysis
(D) Electrolysis
(A) –CN
(B) C = NH
(C) –NH2
(D) –C = NH2
(A) –SH
(B) –COOH
(C) –OH
(D) –CHO
7. CH3–CN is a :
a. Ethyl cyanide
b. Ethane nitrile
c. Methyl amine
d. Methylimine
(A) –OH
(B) R–COOH
(C) R–CO–R
(D) R–O–R
(A) Amine
(C) Ether
(B) Alcohols
(C) Aldehydes
(D) Ketones
(A) An ester
(B) An ether
a. Chain
b. Metamerism
c. Position isomerism
a. Chain
b. Metamerism
c. Position isomerism
(B) Metamers
a. 1-Butene
b. Ethylbromide
c. Butenedioic acid
d. 2-Propenol
a. C2H5Br
b. CH2 (COOH)
c. (CH)2 (COOH)2
d. C2H6
(A) Metamers
a. C6H5–CO–CH3
b. CH3CHO
c. C6H5–CO(CH3)3
d. CH3–CO–CH4
20. Diethyl ketone and Methyl-n-propyl ketone are :
a. Tautomers
c. Chain isomers
d. Metamers
a. Tautomerism
b. Position isomerism
c. Chain isomerism
d. Metamerism
a. Alkanes
b. Alkenes
c. Alkynes
d. Alcohols
a. Metamerism
c. Tautomerism
d. Geometric isomerism
b. Geometric
c. Metameric
d. Skeletal
b. Position isomerism
c. Chain isomerism
d. Metamerism
26. Compounds which have same structural and molecular formula but differ with respect to positions
of the attached groups in space are
a. Geometric isomers
c. Tautomers
d. Position isomers
a. 2,2–Dimethyl propane
b. 2,3–Dimethyl pentane
c. Ethylmethylbutane
d. Dimethyl propane
a. Triphenylmethane
b. 2,2,2 Trimethyl benzene
a. 1-Methyl-2propyne
b. Isobutylene
c. Vinylacetylene
d. 3-Methyl-propene
(A) Primary
(B) methyl
(C) secondary
(D) tertiary
(A) F¯
(B) OH¯
(C) CH3¯
(D) NH2¯
b) The electrophiles are attacked by the most electron-populated part of one nucleophile
c) Chemical species that do not satisfy the octet rule such as carbenes and radicals are electrophiles
d) Electrophiles are Lewis base
a) H2O
b) Cl2
c) HBr
d) Br2
a. BCl3
b. CH3OH
c. NH3
d. AlCl4¯
(A) Primary
(B) methyl
(C) secondary
(D) tertiary
a. Nucleophile
b. Electrophile
c. Free radical
d. Ion
37. An organic compound having functional group –COCl are called :
a. Acyl halide
b. Aryl halide
c. Alkyl halide
d. Vinyl halide
(C) Carbanion
a. Methyl
b. Primary
b. Secondary
d. Tertiary
(A) Electrophile
(C) Nucleophile
a. Ethylene glycol
b. Glycerol
c. Propylene glycol
a. Citric acid
b. Tartaric acid
c. Ascorbic acid
d. Lactic acid
a. Citric acid
b. Tartaric acid
c. Ascorbic acid
d. Lactic acid
KEY
1. B
2. D
3. A Lesser the carbon numbers, greater will be the efficiency but lesser amount of energy will be
produced
4. C
5. C
6. A
8. C
9. D
10. D
11. C R–CO-O-CO–R
12. D C2H5–OH and CH3–OCH3 . Alcohol and ethers are functional group isomers and they follow
CnH2n+2 O. Aldehyde and ketones are functional group isomers and they follow CnH2n O. Carboxylic
acid and esters are functional group isomers and they follow CnH2n O2
13. D C2H5–CHO and CH3–CO–CH3 . Alcohol and ethers are functional group isomers and they
follow CnH2n+2 O.Aldehyde and ketones are functional group isomers and they follow CnH2n O.
Carboxylic acid and esters are functional group isomers and they follow CnH2n O2
16. C Butenedioic can show cis (–COOH on same side) and trans (–COOH on opposite side) isomers.
2–Butene can show geometric isomerism but 1–Butene cannot show. Trans form is more stable due to
opposite presence of bulky groups
17. C
18. D
19. C Bscause it lakes alpha hydrogen. Benzaldehyde and benzophenone do not show tautomerism
due to lack of alpha hydrogen
20. D Because they have same functional groups and do not have difference in their chain structure
however have difference in position of functional group so they can be positional isomers. Due to
unequal distribution of carbon atoms on either side of functional group they are also metamers. In
tautomerism there is shifting of hydrogen so they are not tautomers
21. D
24. D
26. A
27. A
28. A
29. C
30. D Electron poor species are stabilized by neighboring atoms that can donate electron
density. The most common way to interpret rich neighbors here is the observation that
increasing the number of alkyl groups on the carbon bearing the free radical increases its
stability. Radical stability increases in the order. methyl < primary < secondary < tertiary
32. D Because electrophiles accept electrons, they are Lewis acids not Lewis base, according to
Acid-Base reaction theories.
33. C Hydrogen bromide is a strong acid, it is able to donate a proton to a molecule or anion
with a nucleophilic site.
37. A Acyl halide/Acid halide [CH3-CH2-CO-Cl] , Aryl halide/Phenyl halide [C6H5–Cl] , Alkyl
halide [CH3-CH2-Cl] , Vinyl halide [CH2=CH–Cl]
38. C
40. A
41. B
42. D
43. B
HYDROCARBON (ALKANES)
1. Halogenation of alkanes is an example of :
a. Nucleophilic substitution
c. Oxidation reaction
d. Eimenatiom reaction
a. Amount of alkanes
b. Amount of halogen
c. Nature of light
d. Amount of catalyst
3. Function of light in Halogenation of alkanes is :
a. Sunlight
b. Halogen ®
c. Alkane
d. Halide ion
a. Initiation
b. Propagation
c. Termination
6. Methane reacts with HCl under ordinary condition of temperature, which of the following product can
be formed?
a. Methyl chloride
b. Chloroform
c. Carbon tetrachloride
b. CH2Cl2
c. CHCl3
d. All of these
a. Combustion
b. Halogenation
d. Hydrogenation
9. During halogenation, if an excess of methane reacts with chlorine in sunlight to form chloromethane,
what will be the major product?
(B) Dichloromethane
(C) Trichloromethane
KEY
1. B It is also an example of electrophilic substitution reaction because hydrogen atom is removed by
halogen in form of electrophile
2. B
3. A
4. B In the methane molecule, the carbon‐hydrogen bonds are low‐polarity covalent bonds. The
halogen molecule has a nonpolar covalent bond. UV light contains sufficient energy to break the weaker
nonpolar chlorine‐chlorine bond (∼58 kcal/mole), but it has insufficient energy to break the stronger
carbon‐hydrogen bond (104 kcal/mole). The fracture of the chlorine molecule leads to the formation of
two highly reactive chlorine free radicals (chlorine atoms). A free radical is an atom or group that has a
single unshared electron.The bond that is ruptured is said to have broken in a homolytic fashion; that is,
each of the originally bonded atoms receives one electron. This initial reaction is called the initiation
step. This halogen atom(free radical) acts as electrophile
6. D Alkanes are least reactive and give substitution reaction at high temperature
7. B In organic chemistry, a methylene group is any part of a molecule that consists of two hydrogen
atoms bound to a carbon atom, which is connected to the remainder of the molecule by two single
bonds. –CH2–
8. C
9. A Greater the amount of alkane uses, greater will be the amount of alkane in the product. Greater
the amount of halogen uses, greater will be the amount of halogen in the product.
10. A When a chlorine free radical approaches a methane molecule, a homolytic fission of a
carbon‐hydrogen bond occurs. The chlorine free radical combines with the liberated hydrogen
free radical to form hydrogen chloride and a methyl free radical. This is called a propagation
step, a step in which both a product and a reactive species, which keeps the reaction going, are
formed.
HYDROCARBON (ALKENES)
1. Preparation of alkene from alkyle halides is an example of :
a. Substitution reaction
b. Elimination reaction
c. Rearangement reaction
a. Acidic medium
b. Basic medium
c. Alcoholic KOH
d. Aqueous medium
a. OH¯
b. K+
c. Br¯
d. CH3¯
a. Conc. H2SO4
b. Pt
c. Fe
d. V2O5
a. Ethyll alcohol
b. 2-Propanol
c. Propan-1-ol
d. 2-methylpropan-2-ol
7. Which of the following product will be obtained by treating 2-Butanol with conc. H2SO4?
a. 1-Butene
b. 2-Butene
c. 2-methyl butene
a. Ethanol
b. Butanol
c. 2-Butanol
d. 2-methylpropan-2-ol
a. Alkane
b. Alkene
c. Alkyne
d. Alcohol
a. Aqueous
b. Alcoholic
c. Basic
11. In Kolbe's Electrolytic Method of alkene preparation, which product is obtained at anode?
a. H2O
b. NaOH
c. Alkene
d. Na
a. Lindlar's catalyst
c. Methanol
d. P2O5
d. Hydration of alkenes
14. Alkenes undergo:
a. C=C
b. Carbocation
c. Carbanion
a. Isothermal
b. Endothermic
c. Qualitative
d. Quantitative
a. Cyclopentane
b. iso-Pentane
c. Pentane
d. 2-Ethyl Propane
21. Which product will be obtained for the following reaction? Isobutylene + HBr -----> X
a. 1-Bromo-2-methylpropane
b. 2-Bromo-2-methylpropane
c. 2-Bromo butane
d. 1-Bromo butane
22. Which product will be obtained for the following reaction if reaction occurs in presence of peroxide or
sunlight? Isobutylene + HBr -----> X
a. 1-Bromo-2-methylpropane
b. 2-Bromo-2-methylpropane
c. 2-Bromo butane
d. 1-Bromo butane
23. Addition of cold concentrated sulphuric acid to alkene to produce alcohol is an example of :
a. Dehydration reaction
b. Hydration reaction
c. Decomposition reaction
d. Elimination reaction
24. The reaction in which addition of halogens in alkene take place via intermediate formation are:
25. Which of the following tests used for detection of a double bond in alkene?
a. Addition of halogen
c. Ozonolysis
d. Addition of oxygen
26. Which of the following tests used for detection of a double bond in alkene
a. Addition of halogen
c. Ozonolysis
d. Hydroxylation
27. In which of the following reactions of alkene, molecules of solvent become reactants too?
a. Alkene ----> Halohydrin
a. Cl–CH2–CH2–OH
b. H3C–CH2–Cl
c. Cl–CH=CH–OH
d. H3C–Cl–OH–CH2
a. Halohydrin
b. Glycols
c. Glyoxal
d. Glycerol
30. Which of the following statement is wrong When alkenes are treated with Baeyer's reagent :
31. Which of the following reaction of alkene give anti freezing agent?
a. Ozonolysis
b. Hydroxylation
c. Halogenation
d. Oxygenation
a. Alcohol
b. Carboxylic acid
c. Ketone
d. Aldehyde
a. Alcohol
b. Carboxylic acid
c. Ketone
d. Aldehyde
a. Hydroxylation
b. Ozonolysis
c. Combustion
a. Acetic acid
b. Formaldehyde
c. Acetaldehyde
d. Ethanol
36. When ethylene ozonoid is treated with Zn dust, we get
a. Ethanol
b. Methanal
c. Acetaldehyde
d. Ethanal
a. Acetaldehyde + Propanone
b. Formaldehyde + Propanone
c. Formaldehyde + Butanone
d. Acetaldehyde + Acetaldehyde
38. What will be the position of double bond when in alkene, acetaldehyde and propanone are formed on
Ozonolysis?
a. C1
b. C2
c. C3
d. C4
39. If H2C = CH2 –CH2 –CH3 is ozonolyzed then which products will be obtained?
a. Acetaldehyde + Propanone
b. Formaldehyde + Propanone
c. Formaldehyde + Butanone
d. Acetaldehyde + Acetaldehyde
b. Lindlar's catalyst
c. Raney Nickle
a. HCl
b. H2SO4
c. S2Cl3
d. SO2
a. Br2/CCl4
b. Baeyer's reagent
c. Tollen's reagent
d. Zn/H2O2
44. Which of the following does not change when ethene is polymerized to polyethylene?
(A) M-P
(B) Density
(C) Molar mass
(D) % composition
(A) 200°C
(C) 300°C
(B) 400°C
(D) 100°C
(A) glycol
(B Acetic acid
(C) Glycerol
(D) Alcohol
(A) Halogenation
(C) Hydrogenation
(B) Hydroxylation
(D) Dehydrogenation
KEY
1. B Dehydrogenation is an elimination reaction that eliminates hydrogen halide from substrate
2. C
3. A
6. C
7. B If there are equal number of carbons on each side of –OH then H will be remove from that carbon which
have low number of carbon. H3C–CH2–CH(OH) –CH3 ---> H3C–CH=CH–CH3
9. B
11. C Alkene and CO2 are produced at anode while NaOH produced at cathode
13. B
14. D Alkenes have loosely held pi-electrons which are more easily exposed to attack by the electrophilic
reagent
15. B First, electrophile attack on C=C and form carbocation and then nucleophile attack on carbocation to
form an addition product
16. D
17. D
18. B
20. D Alkenes have loosely held pi-electrons which are more easily exposed to attack by the electrophilic
reagent
21. B According to Markownikov's rule: The addition of unsymmetrical reagent to an unsymmetrical alkene
24. D Alkenes have loosely held pi-electrons which are more easily exposed to attack by the electrophilic
reagent
25. A
26. C Hydroxylation and halogen addition are used for detection of double bond while Ozonolysis is used for
determination of position of double bond
27. A
28. A
29. B
32. A
35. B
36. B 2 molecules of formaldehyde(Methanal) produced due to equal distribution of carbon atoms on each
side of double bond
37. D 2 molecules of acetaldehyde(ethanal) produced due to equal distribution of carbon atoms on each
side of double bond
41. C
42. A
43. C
44. D
45. C
46. B In cold KMnO4, 2 butene gives glycol while in hot KMnO4, 2 butene gives carboxylic acid (acetic
acid)
47. B
HYDROCARBON (BENZENE)
a. Presence of O2
b. Absence of O2
c. Presence of excess of O2
d. Presence of Hydrogen
3. The C-C and C-H bond lengths in benzene molecule are respectively
a. Nucleophile
b. Strong electrophile
c. Weak electrophile
d. base
a. FeCl3
b. Benzonium ion
c. Halonium ion
d. Tetraheloforate
6. Benzene reacts with HNO3 in the presence of H2SO4 to form nitrobenzene. What is the
volume ratio of HNO3 to H2SO4 used?
a. 1:2
b. 2:1
c. 1:1
d. 1:4
7. Benzene reacts with HNO3 in the presence of H2SO4 to form nitrobenzene. What is the role
of H2SO4?
(A) Solvent
a. Acid
b. Base
c. Catalyst
d. Reducing agent
(A) NO+
(B) NO2+
(C) NO2+
(D) NO2
(A) H2SO4
(B) HSO4
(C) SO3+
(D) SO3
11. Hydrolysis of benzene sulphonic acid with super heated steam or by boiling with dil. HCl gas:
(A) Toluene
(B) Benzene
(C) Xylene
(D) Chlorobenzene
a. To act as an electrophile
b. To generate an electrophile
c. To absorb water
d. To generate a nucleophile
13. The acylation of benzene in presence of an ethanoyl chloride and AlCl3 gives:
c. Benzoyl chloride
d. Benzacetaldehyde
14. The acylation of benzene in presence of an propanoyl chloride and AlCl3 gives:
c. Benzoyl chloride
d. Benzacetaldehyde
a. Cyclohexane
b. Hexabromobenzene
c. Bromobenzene
d. 1,3,5 Bromobenzene
16. Benzene undergoes oxidation by:
a. KMnO4
b. K2Cr2O7
c. Sunlight
d. V2O5
17. The emperical formula of the product which is formed by reaction of benzene with oxygen
in presence of V2O5?
a. C H O
b. C2 H2 O
c. C H2 O
d. C H O2
a. Aldehyde
b. Glycol
c. Glyoxal
d. Glycerol
a. C6 H6 O6
b. C6 H6 O9
c. C6 H6 O5
d. C6 H5 O8
20. Reaction of toulene with chlorine in presence of sunlight and FeCl3 gives:
a. Benzoyl chloride
b. Benzyl chloride
c. m-chlorotoulene
a. Nucleophilic substitution
b. Electrophilic substitution
a. Ozonolysis
b. Halogenation
c. Friedel-Crafts Reaction
a. Ozonolysis
b. Halogenation
c. Friedel-Crafts Reaction
a. Methylbenzene
b. Toulene
c. Propylbenzene
d. Benzene
26. When toluene is oxidized in the presence of KMnO4, the product is:
(A) benzopheone
a. Phenol
b. Toulene
c. Aniline
d. Nitrobenzene
28. Which one is more reactive specie?
(A) Phenol
(B) Nitrobenzene
(C) Toulene
(D) Chlorobenzene
29. Which of the following group, increases the chemical reactivity of benzene toward
electrophilic substitution reaction?
a. –NO2
b. –CN
c. –COOH
d. –CH3
30. Which of the following group, increases the chemical reactivity of benzene toward
nucleophilic substitution reaction?
a. –CH3
b. –CHO
c. –NH2
d. –OH
31. Which of the following is o-p but rather than electron donating, it is electron withdrawing
group?
a. –CHO
b. –NH2
c. –OCH3
d. –Cl
32. Which of the following undergoes nucleophilic substitution reaction most easily?
a. Chlorobenzene
b. Benzene
c. m-Chloronitrobenzene
d. p-nitrotoulene
33. If toulene is treated with HNO3 and H2SO4 at low temperature, which of the following
product may be formed?
a. o-nitrotoulene
b. p-nitrotoulene
d. m-nitriotoulene
c. m-chloronitrobenzene
d. m-nitrochlorobenzene
d. m-nitrochlorobenzene
a. p-bromobenzaldehyde
b. o-bromobenzaldehyde
d. m-bromobenzaldehyde
37. Benzene + Hydrogen -----> Cyclohexane . The conditions to carry out that reaction:
a. Ni/H2O
b. Pt/CH3COOH
c. Pt at 1000°C
d. Ni-Al at 1000°C
38. Which of the following products will be obtained if following reaction is carried out in acidic
medium? C6H6 + SO3 ----->?
a. Aniline
b. Phenol
d. Toulene
a. H2O
b. HNO3
c. SO2
d. SO3
a. Chlorobenzene
b. Toulene
c. Aniline
d. Phenol
a. Friedel-Crafts reaction
b. Halogenation
42. Which of the following organic compound cannot be prepared directly from benzene?
a. Nitrobenzene
b. Cyclohexane
d. Phenol
(A) Nitration
(B) Sulphonation
(C) Hydrogenation
(D) Bromination
KEY
2. B
3. B
4. B The highly stable, delocalized electrons of benzene ring are not readily available for
nucleophilic attack like electrons of alkenes. Therefore the electronsbof benzene ring are not
attacked by weak electrophiles. It means that more powerful electrophiles are required to
penetrate and break the continuous sheath of electrom cloud in benzene
6. C
7. C
8. B
9. B Nitronium ion
10. D
11. B
13. A Ethanoyl chloride is IUPAC name of acetyl chloride. Methyl phenyl ketone Also known as
Acetophenone . C6H6 + CH3–CO–Cl ----> C6H5–CO–CH3
14. B CH3-CH2-CO-Cl + C6H6 -----> C6H5–CO–C2H4
16. D
18. C Glyoxal have formula C2H2O2. 3 molecules of glyoxal formed by ozonolysis of one
molecule of benzene
19. B
22. D
23. D Benzene cannot produce benzoic acid on oxidation with KMnO4/H2SO4 while toulene
can produce.
24. D Whatever the length of alkyl group may be it gives one carboxyl group. Benzene directly
cannot produce benzoic acid on oxidation with strong oxidizing agent. Methyl benzene is a
toulene and toulene can produce benzoic acid because it has methyl group
25. D
26. D
27. D Electron withdrawing groups decreasds the reactivity of benzene toward electrophile.
Electron withdrawing groups are those in which key atom( directly attached to benzene ring) is
less electronegative than neighbouring atom. For example in –NO2 , key atom is N and it is less
electronegative than neighbouring O atom. Electron withdrawing group, draw the electron
density towards it and hence make the benzene ring inappropriate for attack of electrophile
28. A Stronger the electron donating group attached, greater will be the reactivity. Electron
donating groups are those in which key atom (directly attached to benzene ring) is more
electronegative than neighboring atom. For example in –OH, key atom O is more
electronegative than neighbouring H atom. Electron donating groups donate charge density to
benzene and make benzene ring appropriate for the attack of electrophile
29. D Electron donating groups increases chemical reactivity of benzene towards electrophilic
substitution reaction. Electron donating groups are those in which key atom (directly attached
to benzene ring) is more electronegative than neighboring atom. For example in –CH3, key
atom C is more electronegative than neighbouring H atom. Electron donating groups donate
charge density to benzene and make benzene ring appropriate for the attack of electrophile
30. B Electron withdrawing group increases chemical reactivity of benzene toward nucleophilic
substitution reaction. Electron withdrawing groups are those in which key atom( directly
attached to benzene ring) is less electronegative than neighbouring atom. For example in –CHO ,
key atom is C and it is less electronegative than neighbouring O atom. Electron withdrawing
group, draw the electron density towards it and hence make the benzene ring inappropriate for
attack of electrophile but make benzene ring more susceptible for the attack of nucleophile
31. D Halogens are o-p but are electron withdrawing group due to resonance effect
32. C Electron withdrawing groups make benzene ring more susceptible for the attack of
nucleophile. Greater the number of electron withdrawing groups attached, greater will be the
reactivity of benzene for nucleophilic substitution reaction. In option A, only one (–Cl) group is
electron withdrawing. In option B there is no electron withdrawing group. In option C, there are
two electron withdrawing groups. (–Cl and –NO2). In option D, there is one electron
withdrawing group (–NO2) and one is electron donating group (–CH3)
34. C Because Nitrobenzene has –NO2, a meta directing group. Groups are named
alphabetically
38. C
41. A Alkyl benzene are produced by Alkylation (Friedal crafts reaction) and converted into
benzoic acid on oxidation with K2Cr2O7 or K2MnO4
42. D Nitrobenzene obtained directly by nitration. Cyclohexane obtained directly by
hydrogenation. Benzene sulphonic acid obtained directly by sulphonation. Phenol cannot be
prepared directly. First, sulphonation of benzene gives benzene sulphonic acid then its
hydrolysis gives phenol
ALKYL HALIDES
1. Akyl halides are considered to be very reactive compounds toward nucleophiles, because:
a. Acidic
b. Basic
c. Neutral
a. Halide ion
b. Hydroxide ion
c. Hydrogen ion
d. Water
4. Which of the following is most reactive towards attacking nucleophile?
a. CH3–F
b. CH3–Cl
c. CH3–Br
d. CH3–I
6. Which of the following alkyl halide show greater reactivity for SN1 reaction?
a. CH3–CH2–Br
b. CH3–CH2–CH2–Br
c. CH3–CH2–I
d. CH3–CH2–CH2–I
a. SN1
b. SN2
8. If nucleophile attacks on alpha-C then which of the following reaction would occur?
a. SN1
b. SN2
c. E1
d. E2
a. Carbon
b. Hydrogen
c. Halogen
d. Hydroxide ion
a. Br¯
b. OH¯
c. NH2¯
d. CH3 O¯
A) Cl-
B) HSO4-
C) Br-
D) OH-
a. SN1
b. SN2
c. E1
d. E2
13. Consider the following reaction CH3-CH2-Br¯ + OH¯ ----> C2H5OH + Br¯. If we double the
concentration of OH¯ then how would be the rate of reaction be affected?
a. It will be doubled
b. It will be halved
d. It will be quadrupled
14. When a secondary alkyl halide is heated with excess of ammonia the major product will be
15. When ammonia reacts with excess of alkyl halide the final product will be
a. Propanoic acid
b. Propanenitrile
c. Ethanenitrile
d. Methanoic acid
A) Nature of solvent
18. Consider the following reaction CH3-CH2-Br¯ + OH¯ ----> C2H5OH + Br¯. The mechanism of above
reaction is
A) Elimination reaction
20. Which of the following type of mechanism of reaction has 50% inversion and 50% retention of
configuration
A) SN1
B) E1
C) SN2
D) E2
21. In the transition state of SN2 mechanism reaction of alkyl halides, which of the following orbital
hybridization is involved:
(A) sp³
(B) sp²
(C) sp
(D) dsp²
22. The elimination of hydrogen halide molecule from two adjacent Carbon atom of an alkyl halide is
called
(A) Dehalogenation
(B) Dehydrohalogenation
(C) Dehydration
(D) Dehydrogenation
23. In elimination reaction of alkyl halide, which is more susceptible for attack of nucleophile?
a. Alpha C
b. Beta C
c. Alpha H
d. Beta H
a. Acidic media
b. Basic media
c. Aqueous KOH
d. Alcoholic KOH
a. Propane
b. Propene
c. Propanol
d. Propanal
a. Alkene
b. Alcohol
c. Aldehyde
a. E2
b. E1
c. SN2
28. Which of the following product is formed when ethyl chloride is treated with Na in ether?
a. n-Butane
b. Propane
c. Ethane
d. Methane
29. In which of the following reactions of alkyl halide, product will be alkane?
30. Which of the following product cannot be obtained directly from alkyl halide?
a. Alkane
b. Alkene
c. Alkyne
d. Alcohol
31. Necessary condition for the following reaction? C3H7-Cl -----> C3H6
a. Aqueous KOH
b. Alcoholic KOH
c. Zn/HCl
d. Na/ether
(A) 1-butanol
(B) 1-butene
(C) 2-butene
(D) 1-butyne
33. Which of the following product is obtained by reduction of alkyl halide?
a. Alkane
b. Alkene
c. Alkyne
d. Alcohol
a. Tetraethyl lead
c. Ethylsodiumbromide
d. Do not react
35. Tertiary alkyl halides are practically inert to substitution by SN2 mechanism because of
a. Instability
b. Insolubility
c. Inductive effect
d. Stearic hindrance
36. Wurtz reaction involves the interaction of alkyl halide in dry ether with:
a. Na
b. Zn
c. Cu
d. Pt
37. Antiknocking agent is produced by rl:
a. Hydroxylation of Alkene
38. In Wurtz synthesis, alkyl halide react with sodium in - - - - to give Alkanes
a. Alcohol
b. Ether
c. Water
d. Zn/HCl
KEY
1. C
3. A Nucleophile attacks on alkyl halide in SN reactions. In SN reaction, two products obtained. Alcohol
and halide ion
4. D If an electrophile is the attacking reagent then E.N difference suggests that alkyl flourides would be
the most reactive one and if an nucleophile is the attacking reagent then alkyl iodides would be the
most reactive one
5. C
6. C The order of reactivity of alkyl halides for Sn2 reactions relies on which of the halogen atoms is
most weakly bonded to the carbon atom. The weaker the bond, the more easily it is broken, the lower
the activation energy for the reaction and the faster the rate at which it will occur. The carbon-fluorine
bond is perhaps one of the strongest bonds in chemistry, and generally regarded as the strongest in
organic chemistry, meaning alkylflourides are very inert (unreactive). This is due to Fluorine’s extremely
high electronegativity. Conversely, as the halides are descended, they become less electronegative,
making the carbon-halide bonds get weaker as you go down, making them more reactive.
Ethyl iodide is more effective due to less steric effect of methyl group .
Now ,the size of propyl group is greater than ethyl group, so the steric effect of propyl group is slightly
high . Hence propyl iodide is slightly less reactive than ethyl iodide
8. B In E-reactions, nucleophile attacks on beta-hydrogen. Alpha carbon means that carbon which is
directly attached to 2 hydrogen atoms and one halogen. So Alpha cabon is present in primary alkyl
halide not in tertiary alkyl halide. Primary alkyl halide show SN2 reaction
9. A
10. A Poor nucleophile is a good leaving group. Good leaving groups are HSO4¯, Cl¯, Br¯, I¯
11. D Strong nucleophile is a poor leaving group. A nucleophile is a chemical species that donates
an electron pair to an electrophile to form a chemical bond in relation to a reaction.
Electronegativity – “greed for electrons” – is the opposite of nucleophilicity – “giving away
electrons. So less the electronegativity more the nucleophilicity of ion. C. Order of
nucleophilicity in some ions: CH3¯ > NH2¯ > OH¯ > F¯. It is due less electronegativity of C atom
among the N, O, F, and C. Poor leaving groups are OH¯, H¯, NH2¯, CH3O¯
12. A Secondary halide shows SN1 in polar solvent while shows SN2 in non polar solvent. Hydrolysis
means presence of water which is a polar solvent.
13. A The rate law expression R = k[nucleophile] [Alkyl halide]. This says that the reaction rate is directly
proportional to [OH¯] and [CH3CH2Br]. If you increase the concentration of any reactant, the reaction
rate will increase. Increasing the concentration of OH⁻ will increase the rate, because there are more
OH⁻ ions attacking the substrate. Increasing the concentration of CH3CH2Br will increase the rate,
because there are more CH3CH2Br molecules available to be attacked
14. A
15. D
16. A Product A is Propanenitrile(Ethyl cyanide). When Alkyl cyanide are treated with acidic media,
carboxylic acid produced. So propanenitrile will give propanoic acid
17. D Involvement of the nucleophile in the SN1 reaction is after the rate-limiting step. Thus, the
nucleophile does not appear in the rate expression. The nature of the nucleophile plays no role in the
rate of the SN1 reaction. Even a weak nucleophile can work in SN1 reaction but stronger nucleophile is
required in SN2. Concentration of nucleophile also does not affect SN1 because it is first order reaction.
R = k [R-X]. Polar solvents stabilize the nucleophile, thereby lowering its energy. This will raise the
activation energy of the reactions.SN2 reactions are not favored by polar solvents. Polar solvents
selectively solvate cations. This raises the energy of the anion (nucleophile), thus making it more
reactive. SN1 reactions are favored by polar solvent The order of reactivity of the alkyl halide in the SN1
reaction exactly parallels the carbocation stability. Tertiary carbocation are more stable than primary
and secondary.
18. B
19. D
21. B
22. B
23. D
24. D
25. B Alkyl halide gives alcohol with aqueous KOH and Alkene with alcoholic KOH
26. D This reaction will not take place because beta hydrogen is absent
27. D Molecules are inverted during a reaction, so they rotate plane polarized light
30. C
31. B
32.
33. A Reduction >> Alkane , Substitution >> Alcohol , Elimination >> Alkene
34. A
35. D
36. A
37. B Hydroxylation of Alkene gives anti freezing reagent. Reduction of alkyl halide with Na/Pb alloy
gives Tetraethyl lead, Tetramethyl lead which are used as an anti–knocking agent
38. B
ALCOHOLS
a. Cyclohexanol
b. 2-Butanol
c. Benzyl alcohol
d. 2-Buten-1-ol
a. Cyclohexanol
b. 2-Butanol
d. Butan-2-ol
a. Methyl alcohol
a. Primary alcohol
b. Secondary alcohol
d. Tertiary alcohol
a. Methyl alcohol
b. Ethyl alcohol
c. Isopropyl alcohol
a. V2O5
b. Al2O3
c. Cr2O3
d. Pt
6. Which of the following organic compound can be prepared from water gas in presence of Zno+Cr2O3
at high temperature and pressure?
a. Wood spirit
b. Ether
c. Alkyl halide
d. Grain spirit
c. Fermentation
d. Distillation
a. Zymase
b. Diastase
c. Urease
d. Invertase
a. 10-20°C
b. 15-25°C
c. 20-30°C
d. 25-35°C
a. 10%
b. 14%
c. 16%
d. 95%
A) Rectified spirit
B) Absolute alcohol
C) Power alcohol
D) Methylated spirit
13. Absolute alcohol may be obtained from rectified spirit by the use of:
a. CaCl2
b. CaO
c. C6H6
d. Mg
a. Methanol
b. Pyridine
c. Acetone
d. Water
a. Ethanol
c. Wood spirit
d. Methanol in water
a. Methanol
b. Propanol
c. Butanol
d. Pentanol
17. Ammonia reacts immediately with:
a. Primary alcohol
b. Secondary alcohol
c. Tertiary alcohol
a. Water
b. Alcohol
c. Acid
d. Pyridine
a. Aldehyde
b. Ketone
c. Alkene
d. Alkyne
21. When 2-pentanol undergoes oxidation with acid dichromate, the product is :
a. Pentanal
b. 2-pentanone
c. 3-pentanone
d. Pentanoic acid
22. What will be the product formed when 2-methyl-2-propanol reacts with K2Cr2O7/H2SO4?
(A) Propanone
a. Carbocation
b. Carbanion
c. Carbene
d. Free radical
24. Treatment of propene with cold concentrated H2SO4 followed by boiling water forms:
(A) Propyne
(B) 1-propanol
(C) Propanal
(D) 2-propanol
25. The dehydration of alcohol in the presence of Conc. H2SO4 at 170° involves:
(A) Free radical intermediate
(A) 1-Butanol
(C) Butanone
(D) 2-Butanol
27. When ethanol reacts with excess of conc. H2SO4, product will be
a. Ethene
b. Ethoxy ether
c. Methoxy ether
d. Ethyne
28. When excess of ethanol reacts with conc. H2SO4, product will be
a. Ethene
b. Ethoxy ether
c. Methoxy ether
d. Ethyne
30. In the reaction : C2H5OH + PBr5 ---> C2H5Cl + POCl3 + HCl. Oxygen attacks :
a. C
b. H
c. P
d. Br
31. Which of the following products are formed by reaction of C2H5OH with PCl5?
a. C2H5Cl + H3PO4
c. C2H5Cl + HCl
d. C2H5Cl + H2PO4
32. Which of the following tests indicate the presence of -OH group?
a. Action of PCl5
b. Action of Na
c. Acylation
d. All of these
33. Which of the following is more reactive when O-H bond breaks?
(A) P° alcohol
(B) T°alcohol
(C) S° alcohol
35. Which of the following alcohol reacts immediately with Lucas Reagent?
a. Isobutyl alcohol
b. 2-butanol
d. 2-Methyl-2-propanol
a. Lucas Test
b. Aqueous Br2
c. Acetyl chloride
d. Zn/Pt
A) Tollen’s reagent
B) Fehling’s solution
C) l2 + NaOH
D) AgNO3(aq)
38. Which of the following type of alcohol is prepared from inorganic source
A) Methanol
B) Ethanol
C) 1-propenol
D) 1-butanol
KEY
1. C Cyclohexanol is a secondary alcohol. Benzyl alcohol is C6H5–CH2-OH. 2-Buten-1-ol is a primary
unsaturated alcohol
3. A The hydroxyl group of a primary alcohol is more “exposed” than it is in a secondary alcohol (which
is flanked by two bulky alkyl groups), so it will be better able to hydrogen bond with other alcohols (the
same goes for secondary vs tertiary alcohols). And better hydrogen bonding means the intermolecular
forces take more energy to overcome, thus a higher boiling point
4. A –CH3 group is an electron donating group. Lesser the methyl group attached to hydroxyl group,
lesser will be the charge density transfer to oxygen and hence lesser will be the holding power of oxygen
to hold hydrogen. In result greater will be the protonating power.
5. C
7. C
8. D
9. D
10. B
11. B
12. B
13. B
14. D
15. B
16. D Greater the methyl groups, greater the solubility in non polar solvent. Lesser number of methyl
groups, greater will be the solubility in polar solvent
18. Alcohol shows two type of reaction. First One in which C–O bond of alcohol breaks(nucleophilic
substitution). 2nd one in which O-H bond of alcohol breaks(electrophilic substitution). In option C, O-H
bond is broken.
19. D
21. B
22. C
24. Dehydration of alcohol (elimination reaction) gives alkene. Hydration of alkene (electrophilic
addition reaction) gives alcohol. Hydration of ethene gives ethanol. Hydration of propene gives 2-
propanal. [Hydration of propene in the presence of dilute sulphuric acid will result in the formation of a
carbocation as an intermediate. It is known that secondary carbocation is more stable than primary
carbocation. Thus, the hydroxide ion will attach to the secondary carbon of propene] Simple you can say,
nucleophile will attack that carbon which was attached to other carbon by double bond and having less
number of hydrogen atoms(swcondary carbon).
26
27. A
28. B
30. C Oxygen attacks phosphorus, displacing one of the bromide (Br¯). Then Br¯ attacks from back side
(SN2 reaction) on carbon. Because C-O bond breaks therefore is is substitution reaction
31. B
32. D CH3OH + PCl5 ----> CH3Cl + POCl3 + HCl
33. A
36. A
38. A
PHENOL
a. Carbolic acid
b. Benzoic acid
c. Benzene
d. Nitrobenzene
a. Carbolic acid
b. Carbonic acid
c. Water
d. Alcohol
a. –OH group
b. Benzene ring
c. Hydrogen bond
(B) m-position
a. Ethanoyl chloride
b. Sodium chloride
c. Propanoyl chloride
d. Nitric acid
7. Which one of the following is more acidic?
a. CH3–COOH
b. C2H5–OH
c. C2H5–SH
d. Picric acid
a. Phenol
b. o-nitrophenol
c. p-nitrophenol
a. Phenol
b. o-nitrophenol
c. p-nitrophenol
10. Which concept best explains that o-nitrophenol is more volatile than o-nitrophenol
a. Resonance
b. Hyper conjunction
c. Steric hinderence
d. Hydrogen bonding
a. Ether
b. Alcohol
c. Toulene derivative
d. Phenol derivative
13. By reacting phenol with bromine water, the product obtained is:
(A) O-bromophenol
(B) m- bromophenol
(C) p- bromophenol
(D) 2, 4, 6-tribromophenol
(A) Nitration
(B) Sulphonation
(C) Hydrogenation
(D) Bromination
a. Cyclohexanol
b. Cyclohexene
c. Cyclohexane
d. Benzene
a. Lucas reagent
b. Bromine water
c. Aqueous NaOH
d. Na
a. 2,4,6 trinitrophenol
b. 1,3,5 trinitrophenol
c. 1,3,5 trinitrotoulene
d. 2,4,6 trinitrotoulene
b. Reaction with H2
19. Phenol reacts with NaOH to form sodium phenoxide solution which is
a. White in colour
b. Yellow in colour
c. Blue in colour
d. Colourless
KEY
1. A Electron donating group makes benzene ring more reactive toward electrophile substitution
reaction. Carbolic acid(phenol) has electron donating group (–OH) while benzoic acid and nitrobenzene
have electron withdrawing groups –CHO and –NO2 respectively.
3. D
4. A Phenol is less reactive toward Nucleophile because phenol has electron donating group (–OH)
which donate charge density to benzene and make it more susceptible for the attack of electrophile. so
nucleophile attack is less favoured
5. A
8. C Electron withdrawing group increases the acidity of benzene derivatives. o-nitrophenol and p-
nitrophenol both have same electron withdrawing group (–NO2). But in o-nitrophenol, -OH and -NO2
are closer to each other so they will form hydrogen bond due to which protonating power of o-
nitrophenol will decrease. On the other hand, in p-nitrophenol, -OH and -NO2 are far from each other so
has more protonating power hence it is stronger acid.
10. D o-nitrophenol has intramolecular hydrogen bonding while P-nitrophenol has intermolecular
hydrogen bonding so boiling point of p-nitrophenol is more
11. A
12. D
13. D
16. D Alcohol reacts with Lucas reagent but phenol does not react. Phenols react with bromine water
to give a white ppt. of 2,4,6-tribromophenol (discussed in Electrophilic substitution in phenol). Alcohols
do not have any action with bromine water. Phenols react with aqueous NaOH to form phenoxide ion
(C6H5O−). Alcohols do not react with aqueous NaOH. Phenols turn blue litmus red. Alcohols do not have
any effect on paper. Both reacts with Sodium. C2H5OH + Na ---> C2H5O¯Na+ + H2 .
C6H5OH + Na ---> C6H5O¯Na+ + H2
17. A
18. A Phenol reacts with alkalies to form salt. C6H5-OH + NaOH -----> C6H5-O¯Na+ (sodium phenoxide)
19. D
a. Aldehyde
b. Ketone
c. Ether
d. Alkane
3. All of the following are in liqued state except?
a. Methanal
b. Ethanal
c. Propanal
d. Butanal
a. No lone pair
b. 1 lone pair
c. 2 lone pairs
d. 4 lone pairs
a. 8%
b. 52%
c. 40%
d. 25%
a. Formaldehyde
b. Formalin
c. Acetaldehyde
d. Paraaldehyde
b. K2Cr2O7 + H2S
c. Na2Cr2O7 + H2SO4
d. Na2Cr2O7 + NO2
8. The oxidation product of ethanol / (K2Cr2O7-H2SO4) is treated first with calcium and then subjected
to distillation under dry conditions, the final product is
A) Acetic acid
B) Propanone
C) Ethanol
D) acetone
A) Calcium acetate
B) Acetic acid
C) Calcium formate
D) Formic acid
10. When calcium acetate is distilled with calcium formate, which product is formed?
a. Acetone
b. Methanal
c. Ethanal
d. Propanal
a. Ketone
b. Aldehyde
c. Alcohol
d. Acid
c. Reduction reactions
d. Oxidation reactions
a. Strong electrophile
b. Weak electrophile
c. Strong nucleophile
d. Weak electrophile
(A) Base
(B) Acid
(C) Electrophile
(D) Nucleophile
16. The least reactive compound towards nucleophilic addition reaction among the following is
A) C6H5CHO
B) CH3CH2CHO
C) CH3CH2COCH3
D) CH3CHO
a. HCN
b. NH2OH
c. NH2 NH2
d. C6H5NH NH2
a. Acidic medium
b. Basic medium
c. Alcoholic medium
d. Aqueous medium
19. Which of the following organic compound gives lactic acid on reaction with NaCN/HCl?
a. Formaldehyde
b. Acetaldehyde
c. Acetone
d. Ethanol
c. Neutral reaction
a. OH¯
b. CN¯
c. Cl¯
d. H¯
a. Tartaric acid
b. Lactic acid
c. Acetic acid
d. Aspartic acid
a. Ethanal
b. Acetamide
c. Ethanoic acid
d. All of these
25. Which ketone will yield tertiary butyl alcohol on treatment with CH3MgBr following by hydrolysis
A) 2-Butanone
B) 3-Pentanone
C) Acetone
D) 2-Pentanone
a. Acetone
b. Formaldehyde
c. Acetaldehyde
d. 3-Pentanone
27. In addition of sodium bisulphite to aldehyde, carbon of carbonyl group makes bond with which atom
of sodium bisulphate?
a. Oxygen
b. Sulphur
c. Sodium
d. Hydrogen
28. Which of the following will not give addition reaction with NaHSO3
(A) HCHO
(B) CH3CHO
(C) CH3-CH2-CHO
(D) CH3-CH2-OH
30. Small methyl ketones and large methyl ketones can be distinguished by treating them with:
a. HCN
b. NaHSO3
c. AgNO3 + NaOH
d. Grignard reagent
a. Ketone
b. Aldehyde
c. Hemiacetal
d. Alcohol
a. Base
b. Acid
c. Reducing agent
a. 50% NaOH
b. H2O
c. Grignard reagent
d. Acid
a. Formaldehyde
b. Acetaldehyde
c. Crotonaldehyde
d. Propionaldehyde
a. Formaldehyde
b. Acetaldehyde
c. Benzaldehyde
d. Trimethylacetaldehyde
37. Compound X reacts wit halogen in presence of NaOH/I2 and form compound Y which on hydrolysis
gives formic acid. In this reaction compound X indicates?
a. Ethanol
b. Formaldehyde
c. Propanol
d. Acetone
a. 1-Pentanol
b. 2-Pentanone
c. 3-Pentanone
d. Pentanal
a. Oxidation reaction
b. Reduction reaction
c. Elimination reaction
d. Hydration reaction
40. Which of the following organic compound cannot give iodoform test?
a. Acetaldehyde
b. Ethanol
c. Acetone
d. Pentanal
a. Iodoform test
b. Lucas test
d. 2,4–DNPH
KEY
1. B
3. A
4. C Oxygen carries partial positive charge due to presence of two lone pairs
5. B
6. B
7. C
8. D Ethanol ---> oxidation ---> Acetic acid ---> reaction with Ca ---> CH3COOCa ---> Distillation --->
Acetone
9. C Distillation of calcium acetate gives acetone. Distillation of mixture of calcium acetate and calcium
formate gives Ethanal(acetaldehyde)
10. C Distillation of calcium acetate gives acetone. Distillation of mixture of calcium acetate and calcium
formate gives Ethanal(acetaldehyde)
11. A
12. A
13. C
14. C
15. C
16. C Ketones are less reactive than aldehydes due to stearic hindrance. If we have to compare to the
reactivity of aldehydes then that one will be more reactive which have less number of methyl groups.
For example Formaldehyde is more reactive than acetaldehyde
19. B
20. A
21. B
23. B
25. C
26. D Ketones in which both alkyl groups are larger than methyl, they do not react sodium bisulphite
27. B Because sulphur atom is more nucleophile than oxygen hence it attacks as a nucleophile on
carbonyl carbon.
28. D Only Aldehydes and small ketones give addition product with NaHSO3
29. B NaHSO3 is used to distinguish aldehydes from alcohols becauses alcohols do not give addition
product with NaHSO3. Aldehydes and ketones both give addition product with it. NaHSO3 is also used to
distinguish smaller methyl ketones from larger methyl ketones.
30. B Only small methyl ketones react with sodium bisulphite. Ketones do not react with AgNO3 (Tollen
Test) at all
31. A
32. D
33. A
34. A
35. C
37. A Ethanol oxidize by iodoform reagent to give sodium formate which on hydrolysis give formic acid
39. A Aldehyde and ketones oxidize to form salt of carboxylic acid. Alcohol oxidizes to form salt of
carboxylic acid. Holoform reactions are also substitution reaction.
a. Strong electrophile
b. Weak electrophile
c. Strong nucleophile
d. Weak electrophile
43. When aldehyde or ketone reacts with hydroxylamine the addition product is called as:
a. Amine
b. Imine
c. Oxime
d. Aldol
44. With hydroxalamine, Ethanal form
a. Ethanal hydrazone
b. Ethanaloxime
c. Ethanalamine
d. 2,4–DNPH
a. Crystalline
b. Amorphous
c. Soluble
d. Crystallites
46. Aldehydes and ketones react with 2,4-DNPH solution to give ppt of colour:
a. Yellow or red
b. Orange or red
c. White or red
d. Black or red
a. Na+
b. OH¯
c. H+
d. Cl¯
C) cannizzoar reaction
D) Polymerization
a. Poison
b. Dye
c. Polymer
d. Hypnotic drug
a. Alkynes
b. Carboxylic acid
c. Acetals
d. Haloforms
a. Aldehyde
b. Ketone
c. Diethers
d. Hydroxy aldehyde
52. In the reduction of aldehydes and ketones with sodium borohydrides, which of the following acts as
nucleophile?
a. Hydride ion
b. Tetrahydridoborate ion
c. Alkoxide ion
d. Hydroxyl ion
53. Reduction of CH2=CH-CO-CH3 with sodium borohydride gives which of the following product?
a. CH2=CH-CHOH-CH3
b. CH3-CH2-CHOH-CH3
c. CH3-CH2-CO-CH3
d. CH2=CH-CO-CH3
55. Which of the following ketones will produce only propanoic acid after oxidation by acidified
potassium dichromate?
a. Ethyl-n-propyl ketone
c. Dimethyl ketone
d. Diethyl ketone
a. Methanol
b. Ethanol
c. Propanal
d. Benzaldehyde
57. Which of the following reagent react with both aldehydes and ketones?
a. Tollens reagent
b. Fehling reagent
c. Benedict reagent
d. Grignard reagent
a. Ketones
b. Ethers
c. Acids
d. Aldehydes
a. CuO
b. Cu2O
c. Cu
d. Cu + Cu2O
a. Cannizzaro's reaction
c. Polymerization
(A) 2-pentanone
(B) 3-pentanone
(C) Pentanal
(D) n-pentane
d. Tollen's test
a. Acetone
b. Pentanone
c. Butanone
d. Ethanal
a. Oxidation
b. Phenylation
42. D
43. C
44. B
45. A
46. A
48. D
49. D
50. C
51. C
52. A
54. D In case of symmetrical ketones only carbon atom adjacent to carbonyl group is oxidized and a
mixture of two carboxylic acids is always obtained. For example acetone gives acetic acid and formic
acid. In case of unsymmetrical ketones, carbon atom joined to smaller number of hydrogen atom is
preferabley oxidized and carbonyl group remains with smaller alkyl group. For example Butanone gives
only acetic acid
55. D Diethyl ketone is 3-Pentanone. Ethyl methyl ketone is butanone. Ethyl n propyl ketone is 3-
Hexanone. In case of symmetrical ketones only carbon atom adjacent to carbonyl group is oxidized and
a mixture of two carboxylic acids is always obtained. For example acetone gives acetic acid and formic
acid. In case of unsymmetrical ketones, carbon atom joined to smaller number of hydrogen atom is
preferabley oxidized and carbonyl group remains with smaller alkyl group. For example Butanone gives
only acetic acid. 3-Hexanone gives only propanoic acid.
56. C Aldehydes are stong reducing agent. Propanal is easily oxidized due to –C-H group and small size
57. D
58. D
59. B
62. B Both aldehydes and Ketones form phenylhydrazones. Aldehydes also react with Tollens reagent.
Ketones do not react with Tollens reagent. Now from given options, 2-pentanone and 3-pentanone both
do not react with Tollen reagent but 2-pentanone give iodoform form test positive due to presence of
CH3 group attached to carbonyl carbon [CH3-CH2-CH2-CO-CH3] but 3-pentanone gives iodoform test
negative due to absence of CH3 group attached to carbonyl carbon [CH3-CH2-CO-CH2-CH3]
63. D Aldehydes react with Tollen Reagent. Ketones do not react with Tollen reagent.
64. C
CARBOXYLIC ACIDS
1. Which acid do not contain - COOH groups?
a. Ethanoic acid
b. Ethanedioc acid
c. Propanoic acid
d. Propanedioc acid ®
(D) H-bonding
4. When carboxylic acid is dissolved in non polar solvent such as benzene it exist as cyclic dimmers and
shows _________ membered ring
A) 6
B) 8
C) 10
D) 12
5. Which of the following carboxylic acid does not have pungent smell?
a. Methanoic acid
b. Propanoic acid
c. Butanoic acid
d. Ethanoic acid
6. Which one of the following carboxylic acid has highest boiling point?
a. Methanoic acid
b. Propanoic acid
c. Butanoic acid
d. Ethanoic acid
7. Which one of the following carboxylic acid has highest melting point?
a. Ethanoic acid
b. Propanoic acid
c. Butanoic acid
d. Pentanoic acid
a. Ethanoic acid
b. Propanoic acid
c. Butanoic acid
d. Pentanoic acid
a. Flouroacetic acid
b. Chloroacetic acid
c. Bromoacetic acid
d. Iodoacetic acid
a. F-CH2-COOH
b. Cl2-CH-COOH
c. Br-CH2-COOH
d. I2-CH-COOH
11. The weakest acid is :
a. CH3COOH
b. ClCH2COOH
c. Cl2CHCOOH
d. Cl3COOH
a. CH3-CH2-CH2-CH2-COOH
b. F-CH2-CH2-CH2-CH-COOH
c. CH3-CH(F) - CH2-CH2-COOH
d. CH3-CH2-CH2-CH(F)-COOH
a. CH3-CH2-CH2-CH2-COOH
b. F-CH2-CH2-CH2-CH-COOH
c. CH3-CH(Cl)-CH2-CH2-COOH
d. CH3-CH2-CH2-CH(Br)-COOH
(A) HCOOH
(B) CH3CH2COOH
(C) CH3COOH
(D) ClCH2COOH
(A) Phenol
(B) Ethanol
b. Acid-base reaction
c. Nucleophilic substitution
d. Electrophilic addition
19. Ethanoic acid reacts with all of these to produce water except?
a. Sodium
b. Ethanol
c. Caustic soda
20. All of the following reactions of carboxylic acid are electrophilic substitution except?
21. Acids form sodium salt with evolution of CO2 on treatment with :
a. Sodium metal
b. Soda lime
c. Sodium carbonate
d. Sodium hydroxide
22. CH3COOH + Ca ----> CH3COOCa + H2 . This given reaction proceeds through which mechanism?
24. Conversion of Acetic acid into an acetyl chloride by treating it with Thionyl chloride is an example of :
25. CH3COOH + SOCl2 ----> CH3COCl + SO2 + HCl . In this reaction ----- attacks on Electrophilic carbon?
a. Cl¯
b. S¯
c. O¯
d. H¯
26. CH3COOH + SOCl2 ----> CH3COCl + SO2 + HCl . In this reaction Cl¯, attacks on :
a. Methyl carbon
b. Carbonyl carbon
c. Hydroxy Hydrogen
d. Carbonyl Oxygen
27. Carboxylic acid can be changed to acid chloride by the treatment with:
(A) S2Cl2
(B) SOCl2
(C) HCl
(D) HOCl
28. Which product is not formed when acetic acid reacts with SOCl2?
(A) CH3Cl
(B) CH3COCl
(C) HCl
(D) SO2
29. Which of the following will react with both ethanol and ethanoic acid at room temperature?
(A) CaCO3
(B) CuO
(C) Na-metal
(D) CH3OH
(A) HCOOH
(B) CH3COOH
(C) (CH3)2CHCOOH
31. When ethanol is treated with acetic acid then which of the following ester is formed?
a. Ethyl formate
b. Ethyl ethonate
c. Ethyl propionate
d. Methyl ethonate
32. When ethanol is treated with formic acid then which of the following ester is formed?
a. Ethyl formate
b. Ethyl ethonate
c. Ethyl propionate
d. Methyl ethonate
a. HCOONa
b. CH3COONa
c. HCOOH
d. CH3COOH
a. Methyl carbon
b. Carbonyl carbon
c. Hydroxyl group
d. Carbonyl Oxygen
a. Methyl carbon
b. Carbonyl carbon
c. Hydroxyl group
d. Carbonyl Oxygen
36. When ethanol is treated with formic acid then which ester is formed?
a. Ethyl propionate
b. Ethyl formate
c. Ethyl ethonate
d. Methyl ethonate
37. The organic compound A and B react with sodium metal and release H2 gas. A and B react with each
other to give ethyl acetate. The A and B are:
(A) Banana
(B) Apricot
(C) Jasmine
(D) Orange
a. Ammonium salt
b. Acetamide
c. Ammonia
d. Cyanide
(A) Acetamide
42. Those compounds in which a water molecule is eliminated from two carboxylic groups of same or
different molecules are called:
a. Acid amide
b. Acid imide
c. Acid anhydride
d. Acid halide
(A) H3PO3
(B) H3PO4
(C) HPO3 ®
(D) H4P2O7
44. Unsaturated carboxylic acid on reaction with Lithium aluminium hydride give:
a. Saturated alcohol
b. Unsaturated alcohol
c. Acetic anhydride
d. Saturated ketones
45. Which of the following cannot be prepared directly from carboxylic acid?
a. Alkane
b. Alcohol
c. Ketone
d. Alkene
A) Alkane
C) Benzene
B) Alkene
D) Alkyne
a. Acid chlorides
b. Acid imide
c. Esters
d. Acid anhydride
a. Acid chlorides
b. Acid amide
c. Esters
d. Acid anhydride
49. A compound X on reduction gives alcohol. Compound X has molecular mass of 30 amu. What is the
compound X?
a. Aldehyde
b. Ketone
c. Carboxylic acid
d. Ether
50. X is an organic compound made up of C, H and O. It has vapour density 15. Compound X is :
a. Aldehyde
b. Ketone
c. Carboxylic acid
d. Ether
KEY
1. C
2. D
3. D
4. B
7. C Melting points of carboxylic acids containing even number of carbon atoms are higher than the
next lower and higher members containing odd number of carbon atoms
8. A Greater the methyl group, weaker the acidic strength because methyl group are electron donating
group. Charge density increases on hydroxyl group due to which proton holding capacity of oxygen
increases. Release of proton becomes difficult. Acids which do not realese proton are weak acids
9. A Only halogens are the such o-p directing groups which instead of electron donating are electron
withdrawing group. So they draw charge density from hydroxyl group and proton holding capacity of
Oxygen decreases i.e release of proton becomes easier thus acidic strength increases. Flourine is more
electronegative thats why it greatly increases the acidic strength F-CH3COOH > Cl-CH3COOH > Br-
CH3COOH > I-CH3COOH
10. C because in option D there is diiodoacetic acid. As Number of halogens increases, acidic strength
increases. Two I can withdraw electron density greatly as compared to single more electronegative Br
11. A In option A there are only methyl group whichbare electron donating makes tue acid weak
12. D Nearer the halogen to the hydroxyl group, greater the withdrawing effect and stronger will be the
acidic strength
13. D Nearer the halogen to the hydroxyl group, greater the withdrawing effect and stronger will be the
acidic strength
16. D Carboxylic acid > Phenol > Alcohol . Lesser the number of methyl groups, stronger will be the acid.
18. A
20. D In first three options, O-H bond of carboxylic acid breaks. Its hydrogen releases as an electrophile.
22. A Because O-H bond of carboxylic acid breaks. Hydrogen is substituted by metal calcium.
25. A
27. B
28. A
31. B C2H5OH + CH3COOH ---> CH3COOC2H5 + H2O . Ethyl ethonate or Ethyl acetate is produced
36. B
37. A Alcohol and Carboxylic acid both react with metal and give H2. They react with each other to give
ester. C2H5OH + CH3COOH ---> CH3COOC2H5 + H2O
38.
41. A First ammonium salt is formed which later on dehydration gives acidamide
42. C
43.
45. D
46. A
47. B
48. A Acid chloride > Acid anhydride > Ester > Acid amide
49. A Aldehyde, ketone and carboxylic acid give alcohol on oxidation. 30 amu is not possible for ketone
and carboxylic acid because molecular mass of their lowest members i.e Formic acid (46amu) and
Acetone (58amu). Only aldehydes have a member of molecular mass of 30amu and that one is
formaldehyde
1. The peptide bond which is formed by the condensation of amino acids is what type of
bond
A) ester
B) amide
C) ether
D) Anhydride
A) Glycine
B) Histidine
C) Lysine
D) Aspartic acid
A) Peptide
B) Polypeptide
C) Protein
D) Dipeptide
4. The amino acid which was first isolated from cheese is:
A) Glycine
B) Tyrosine
C) Lysine
D) Valine
A) Optimum pH
B) Isotonic point
C) Isoelectric point
D) Azeotropic point
6. All the amino acids are asymmetric and show optical isomerism except:
A) Valine
B) Tyrosine
B) Glycine
D) Alanine
8. The amino acids are different from each other due to:
A) Lysine
C) Tyrosine
B) Histidine
D) Glycine
(A) Alanine
(B) Glycine
(D) Aniline
(A) Lysine
(B) Glycine
(C) Alanine
(A) Alanine
(B) Aniline
(C) Analine
(D) Aspartic acid
(B) It is a salt
(A) -COOH
(B) -NH2
(C) NH3+
(D) NH3
16. When an alkali is added to the aqueous solution of an amino acid, net charge on a molecule of amino
acid is:
(A) +ve
(B) Zero
(C) -ve
(A) Lysine
(B) Alanine
(C) Asparagine
(D) Glutamine
20. In aqueous media that contains alanine and HCl, the distribution of charges:
c. Cations = Anions
d. No charge
21. The IUPAC name of Valine is
a. Proline
b. Histidine
c. Lysine
d. Valine
23. Which of the following amino acids has two amino groups?
a. Glycine
b. Alanine
c. Proline
d. Lysine
a. Proline
b. Lysine
c. Glycine
d. Alanine
b. Anion
c. Zwitter ion
d. Neutral system
a. Glutamic acid
b. Aspartic acid
c. Valine
d. Lysine
a. NH2–CH2–COOH
b. NH2–CH2–COO¯
c. COOH–CH2-NH3+
d. COO¯–CH2–NH3+
KEY
1. B
3. B
4. B
8. D
9. B
11. B
13. B
14. B
16. C When an alkali/base is added to an amino acid, –NH3+ releases proton and Zwitter ion exists in
anionic form
17. B
18. C
19. B
21. D
22. B
24. B Glycine, Alanine and Proline are non essential amino acid. Body can synthesize them itself. These
amino acids are also examples of Neutral amino acids
25. A Low pH means acidic medium. In acidic medium amino acid exist as cation
ABDUL MANAN