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CHEMISTRY

Target : JEE MAIN 2020

Final 100 Question Bank


for
JEE Main 2020 by
SY SIR

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2 Physics
Chemistry
GOC
1. Compound which is unstable at roo temperature

O
(A) + (B) (C) O (D)
N N
H H
2. Molecule among the following can not show resonance :
(A) CO2 (B) H2C = C = CH2 (C) N3H (D) CH2N2
3. The correct order of C–N bond length order is

(I) NMe2 NMe2


NO2 NMe2
NO2 (II) (III) NO2
(A) II > I > III (B) III > II > I (C) I > II > III (D) II > III > I
4. Decide most stable resonating structure among following :

(A) (B) (C) (D)

NH2 NH2 NH
NH2 + 2

5. Decide most reactive compound towards electrophilic substitution reaction :


O
CH 3 NO2 Cl
C OPh
(A) (B) (C) (D)

6. The order among following is incorrect :

(A) > > > (HOC Order)

(B) > > > (HOH order)

+ + +
(C) > > > (Resonance energy order)
+

(D) > > (HOH per  bond order)

7. Select the correct order of basic nature among following :


(A) CH3 > NH2 > HO > F (B) F > Cl > Br > I

(C) SH > OH > Cl > F (D) NH2 > H C C > HO > I

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Detol + (B)
8. aq NaOH
  (A)
solution

salt
Compound (A) is :
(A) (A) is Salt of Chloroxylenol (B) (B) is Salt of Chloroxylenol
(C) (A) is Salt of Terpineol (D) (B) is Salt of Terpineol

9. The reaction among following is possible in forward direction :


 
(A) CH3–CH2–CCH + NaOH  CH3–CH2–C  C Na 
 
(B) CH3CH2–CCH + NaNH2 CH3–CH2–C  C Na 
   
(C) CH3  COO Na + ph–OH CH3–COOH + ph  O Na
 
(D) CH 3  SO3 Na + HCl CH3–SO3H + NaCl

10. Match the column :


Column - I Column - II
COOH
CH3
(A) (P) React with Na

OH
(B) O2N NO2 (Q) React with NaOH

NO2
OH

(C) (R) React with NaHCO3

HO O

(D) (S) React with NaNH2

HO O
Passage for Q. 11 and 12
The concept of resonance explain various properties of compounds. The molecules with conjugated systems of
bonds are stabilised by resonance and have low heat of hydrogenation. Hyper conjugative stabilisation also decreases
heat of hydrogenation. In aromatic rings a functional group with a lone pair exerts +M effect.
11. The correct order of heat of hydrogenation -
(p) 1,3-pentadiene (q) 1,3-butadiene
(r) 2, 3-dimethyl-1,3-butadiene (s) propadiene
(A) p > q > r > s (B) s > q > p > r (C) q > s > p > r (D) s > p > q > r

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4 Physics
Chemistry
12. In which option among following I canonical structure is more stable than II-

(A)
N
..
N
I II

O O
(B)
N N
H H
I II

(C)

CH2
CH2
I II

(D) CH2 – C  CH CH2 = CH = CH


I II

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ISOMERISM
13. Identify ‘R’ and ‘S’ configurations of chiral centres in the following compound and select correct option.

(1) (1R) , (2S) (2) (1R) , (2R) (3) (1S) , (2R) (4) (1S) , (2S)
14. Identify compound having highest heat of combustion :

15. Among the following compounds which is resolvable

16. Total number(s) of chiral stereoisomers in 2, 3, 4- trichloropentane :


(1) 0 (2) 2 (3) 4 (4) 6

17.

(1) Enantiomers and geometrical isomers


(2) Enantiomers but not geometrical isomers
(3) Geometrical isomers but not enantiomers
(4) Optically inactive homomers.

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6 Physics
Chemistry
18. Which of the following order is incorrectly matched with given properties.

19. The pair among following representing incorrect relationship

20. Select the pair among following not representing position isomerism:

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21. The compound among following can not show geometrical isomerism:

22. Total number of stereoisomers in benzenehexachloride.


23. If total number of Stereoisomers in Hexa-2,5-diene -4-ol = P & in Hepta-3-ene-2, 6-Diol = Q. Then what will
be value of P × Q ?
24. Match the following :

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8 Physics
Chemistry
HALOGEN DERIVATIVES
25. Degree of unsaturation of compound ‘C’ and F is/are ‘P’ and ‘Q’ then what would be value of Q–P ?
H2SO4 NBS AgF/DMSO
CH2 – OH 
A B C

HBr

Mg/ether B
D E (SN 2 reaction)
F
26. Which one of the following compounds will give enantiomeric pair on treatment with HOH?

C2 H 5 CH 3 H C2 H5
| | | |
(A) C 6 H 5  C  I (B) CH  C  Br (C) C H  C  Br (D) C 2 H 5  C  Br
3 6 5
| | | |
C 2H5 C2 H5 D CH 3
27. In the given reaction
CH 3  CH  CH 2  CH 2  CH  CH 3
| |
OTs OTs

[X]
[X] will be:

OTs S
| | S S
(A) CH 3  CH  CH 2  CH 2  CH  CH 3 (B)
CH3 CH CH2 CH2 CH CH3

(C) (D)

Me SOCl2
Et2O P
28. HO D
SOCl2
Q
H
N
P and Q are respectively
Me Me Me Me

(A) D Cl Cl D (B)
Cl D D Cl

H H H H
Me Me Me Me

H H
(C) Cl D Cl (D) D Cl Cl
H D H D
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CH3
 
18 PCl3 aq.Na O Me
29. H   R
OH 

D
R is
CH3 CH3
18
(A) H O–CH3 (B) H3CO D
D H
CH3 CH3
18
(C) H3CO H (D) H O–CH3

D D
30. Select the incorrect statement about the product mixture in the following reaction :

Br
2  Products
CCl 4
(A) it is optically active (B) it is racemic mixture
(C) it is a resolvable mixture (D) it is a mixture of erythro compounds

31.
OH– Major product.

NMe3

(A) (B) (C) (D)

CH3
Cl
32. alc  I
.KOH
 

Br
H
Major products of above reaction are

CH3 CH3 CH3 CH3


(A) (B)

I I Cl Cl
Cl Cl I I

CH3 CH3

(C) Cl + en (D) I + en
I Cl

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10 Physics
Chemistry
33. In which of the following case configuration about chiral (C) is retained:

Na CH Br SOCl CH ONa
(A)  3 (B) 2  3

1.TsCl
(C) PCl3
  
CH 3ONa
(D) H 2
.MeONa
 
D
34. Which of following reaction products are diastereomer to each other ?

Me
Br2
(A) CH3 
 (B) D H HBr

CCl 4

Ph

(C) HBr
 (D) CH 3  CH  CH  CH  Ph  
HCl
CCl4 peroxide
|
35.
Et
Total number of achiral dibromo product possible when S-2-bromobutane is treated with Br /h in 1: 1 ratio.
2

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ALCOHOL & ETHER
H OHBr HCHO
 B Mg
 /
ether
36. CH3MgBr + 3
  A   C    D 
HI E
H O 3

E is

(A) (B) (C) (D)

37. Consider the reaction of HI with the following:

I II

Which forms di-iodide on reaction with HI (excess)?


(A) I and II both (B) II only (C) I only (D) none

38. P


O OH
P can be
(A) (i) LAH (ii) H2O (B) NaBH4/ EtOH
(C) (i) BH3.THF (ii) CH3COOH (D) All of these
39. In the following reaction, final product is
14
ClCH 2CH  C H 2 NaOC H
 25 
\ /
O
14 14
(A) ClCH 2 CH C H 2 OC 2 H 5 (B) ClCH 2CH C H 2 ONa
| |
OH OC 2 H 5
14 14
(C) C H 2 CHCH 2 OC 2 H 5 (D) C H 2 CHCH 2 OC 2 H 5
O O
18
( i ) H 3C C O  OH
||
O
40.     
 Product(s)
( ii ) OH ¯/ H 2O
18
OH OH OH

(A) + en (B) + en (C) + en (D) + en


18 18
18
OH OH OH OH

41. dil
.alk
.KMnO
 4  Product(s)
Product(s) is / are

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12 Physics
Chemistry
CH3 CH3
(A) OH (B) OH + en
OH H
H OH
CH3
CH3
OH
(C) H (D) H + en
OH
H
H
H / H O
2
42.    J (Major)
J is
OH
OH OH OH
(A) (B) (C) (D)

Et Et O
|| 18
( i ) CH3 C O O  H
43.     
( ii ) H  / H 2 O
D D
Major product(s) of the above reaction is :
Et 18 Et
D OH D OH
(A) + en (B)
18
+ en
HO D D OH
Et Et
Et Et
D OH D OH
+ en
(C) D OH (D)
HO D
Et Et
Cerric ammonium nitrate
Red colour
I2/OH¯
44. P Yellow ppt.
C3H8O
NaHCO 3
CO2
What is structure of P.
O OH
(A) OH (B) O (C) (D)

45. Which of following reaction represent major product.

(A) NaBH
4  (B) NaBH
4 

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(C) LiAlH
4  (D) LiAlH
4 

18
46. Ph  O  Et HI
(excess
 ) Products.
Products are
18
(A) Ph – I + EtI (B) Ph – OH + EtI (C) Ph  O H  EtI (D) None of these

47. Column I Column II


(Reaction) (Major product)

H / H O
2
(A)    (P) OH

(i) Hg (OAc) 2 / H 2 O
(B)    (Q) OH
(ii) NaBH 4 / OH

OH
( i ) BH / THF
(C)  3  (R)
( ii ) H 2O 2 / OH

OH
(S)

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14 Physics
Chemistry
CARBONYL COMPOUND AND CARBOXYLIC ACID
– – 
OH OH H
48. PhCOCHBr2   A  B 
 C
The compound 'C' is
(A) PhCH(OH)CHO (B) PhCH(OH)COOH
(C) PhCOC Br2 (D) None of these
|
H
49. What will be the product of the following reaction
RCO H
Ph(Me)CHCOMe  3 ?

(A) PhC(Me)HOCOMe (B) Ph C —CH


||
O
(C) PhCH(Me)OCOOMe (D) None of these

CH2OH
O H
CH OH HIO
50. OH 3
   X 
4
 Y+Z
dry HCl
OH OH

OH
The product Y is :
CH2OH

O H O OH

(A) CHO (B) CHO


CHO OCH3 CHO OCH3
(C) HCOOH (D) HCHO

 
OH H3 O
51. CH3 COCHO  P   Q

H SO
2Q 2 
4
R

The product R is :
O

C O

(A) CH3 CH(OH)COOH (B) CH3 CH CH CH3

O C

O
O

(C) CH3 CH = CH – COOH (D) CH3 CH C CH3

O OH

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o
OH CH3MgBr Zn– Hg
52. A    B    C
heat Conc.HCl

The product ‘C’

(A) (B) (C) (D)

CH3 COONa HBr


53. PhCHO + (CH3CO)2O    A  B
The product B is
(A) PhCH = CHCH2Br (B) PhCH – CH2– COOH

Br
(C) PhCH2 CH(Br) COOH (D) PhCH = CH – COBr

54. Among the following which one will show significant hydration ?
(I) CCl3CHO (II) (CH3)3CCO(CH3)3

(III) (IV) CH3COCH3

(A) I and III (B) II and III (C) III and IV (D) I and II

55. The end products of following reaction would be,

CHO

HCHO (excess),
NaOH (aqueous)
C
O CH3

CH2OH CH2OH

(A) + HCOONa (B) + HCOONa


C C
O CH3 O C(CH2OH)3

CHO
COONa

(C) (D) + CH3OH

C
C
O C(CH2OH)3
O C(CH2OH)3

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Chemistry
56. The possible number of stereoisomers of the product of following reaction would be :
NH2OH
CH3 – CH = CH – CH – CHO   
|
CH3
(A) 2 (B) 4 (C) 6 (D) 8
57. The final product (C) of the following reactions would be
NH OH HCl . Br / Fe PCl
 2  (A)  (B) 2 (C)
5
C 6 H 5  C  C 6H 5
|| (1) ( 2) (3 )
O

(A) Br C Cl (B) C NH
|| ||
N O
OH Br

(C) C NH Br (D)
||
O

(1) HCl (i) LiAlH 2 3 / Et O H O


58.  X    4    Y   Z, Identify X, Y and Z
( 2) CH2OH (ii) H2O
|
CH2OH
X Y Z
O O
|| || HO CH2OH
(A) O
C–OC2H5 O COC2H5
O

O
|| O
O COOH HO CH2OH
(B) C–OC2H5
O
O

O
|| O O CH2OH
(C) O CH2OH
C–OC2H5
O O

O HO CH2OH HO COOH
(D) CH2OH
O

59. The product obtained in the following reaction is


(1) NOCl / h
    

( 2 ) H2SO4

(A) (B) (C) (D)

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60. The correct sequence of reagents for the following conversion is

SOCl2 Ag 2O CH2N2 SOCl2 CH2N2 (i) Ag 2O/ 


(A)    
H 2O
    (B)     
(ii) H 2O /H

CH N
2 2 2 SOCl
(i) /  Ag Ag 2O SOCl2 CH2N2
(C)     
HO 
(D) 
H 2O
   
(ii) 2 /H
O
O
AlCl3
61.   X+Y

X, Y both responds to FeCl3 test and 2, 4 DNP test. One is thermodynamically controlled product
(TCP) and another is kinetically controlled product (KCP). KCP is
OH OH OH
COR
(A) (B) (C) (D) All of these
COR
COR
62. The following conversion is possible by
Ph – CH2 – CH = O Ph – CH 2 – CH – COOH
|
NH2
(Phenyl alanine)

KCN / H O 3 NH ,  H O , 
2 3
(A)          
KCN / NH Cl H O , 
(B)  4
 3  
HCN / NaOH 2 NH3 SOCl H O , 
   
(C)       3 
Br / CH COOH 3 NH CrO / H
(D) 2  
3 3
       

63. Match the column

Column I Column II


OH
(A) MeCO(CH2)4COMe 

 (p)


OEt
(B) (CH2)4  (q)

(C) PhCHO + 3
 
CH COO –
 (r) (Ph)2 C — COO –
|
OH

OH
(D) PhCOCOPh  (s)

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18 Physics
Chemistry
AMINES
64. Hydrolysis of alkyl isocyanide yields:
(A) Primary amine (B) Tert. amine (C) Alcohol (D) Aldehyde
65. The compound obtained by the reaction between primary amine and aldehyde is:
(A) An amide (B) Imine (C) Nitrite (D) Nitro

Me2 NH
66.   Major product is:

NO2

NMe2 Me F NHMe
NMe2
(A) (B) (C) (D)

NO2 NO2 NO2 NO2

CH 3
| HNO
67. CH 3  CH — C — CH 2  NH 2 2  (X) (major)
| |
CH 3 CH 3
Major product of above reaction is
CH3
CH3
(A) CH C CH2 OH (B)
CH3
CH3 OH

(C) (D)
OH OH
68. Identify X in the reaction
NH2

CHCl / KOH dil HCl


 3  A   X
heat 300 K
Cl

COOH NH2 NC NH2

(A) (B) (C) (D)

Cl COOH Cl Cl

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69. In given reaction sequence.

O
HCl
HCN
 (X) LiAlH
 4  (Y) NaNO
 2  (Z) then
Me
Compound (Z) is:
O O

(A) NH2 (B)


Me Me
NH2
O
O
(C) (D)
Me Me
 –
N2Cl

/
CuCN
 / 
HCN
70.  (A) H   (B) NH
/ H2O
3  (C) B
2H6
 (D)

Correct statement is :
(A) Compound (D) will give phenyl hydrazone with carbonyl compound.
(B) Compound (E) formed is benzoylchloride
(C) Compound (C) formed will give carbylamine test.
(D) Compound (A) & Compound (E) are identical

71. In the reaction shown below, the major product(s) formed is/are

acetic
 anhydride

CH Cl
 Product
2 2

H
N CH3
O + CH3COOH
(A) (B)
NH2
O

H 
N CH3 NH3CH3COO
O + H2O
(C)
H (D)
H
N CH3 N CH3
O O O O

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20 Physics
Chemistry
72. In the given reaction sequence:

( i ) KMnO / O H /  ( i ) SOCl Br / KOH
 (A)  2  (B) 2  (C)
CH3–CH2–OH   4  
(ii ) H  ( ii ) NH 3 / 
(C) will be :
(A) Methylamine (B) Ethylamine (C) Propylamine (D) Acetamide

Me
(i) H /HN
3
Et COOH + (A)
(ii) H3O
(P)
73. H
NH/3  Br/NaOH
2
(B) (C)
Choose the correct statements :-
(A) Products (A) and (C) are identical
(B) Products (A) and (C) have different configuration
(C) Product (A) and (C) are enantiomers
(D) (C) can give compound having unpleasant smell on reaction with CHCl3/OH¯

PARAGRAPH (74-76)

NO2

Sn / HCl
 (X) NaNO
 2
0 C
/ HCl
  (Z) H
 (Y) CuCN / HCN / H 2O
   (W)

74. The structure of compound(X) are:


 – NH2 OH
N2Cl NH2

(A) (B) (C) (D)


H2N NH2
NH2
75. Compound(Y) on heating with CuCl will produce

 –
Cl N2Cl NH2 CN

(A) (B) (C) (D)

76. The compound(W) on reaction with Methyl alcohol will produce


O O
|| ||
(A) CH 3  C  O  CH 3 (B) Ph  C  O  CH 3
(C) Ph  C  O  Ph (D) Ph – N = C = O
||
O

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77. Number of reactions which can produce 1° amine are :

(I) R – C – NH2 OH / Br
 2 
O
O

(i) OH–
(II) N – H (ii) R–I

(iii) OH/H2O

O
NH
(III) CH3 2 H / H O
  
O
(IV) N+ C +
H /H2O

NH–Et H/ H2O
+

(V)
O
N3H/conc. H2SO4
(VI) 
COOH
(VII) C N +
H/ H2O

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22 Physics
Chemistry

AROMATIC COMPOUND & HYDROCARBON


OH
O
||
78. ( i ) CH 3 C Cl
    Major product
(ii ) AlCl3 , 

O
O OH
(A) C–CH3 (B)
C–CH3
O
O OH

CH3 H3C
(C) (D)
CH2OH O

Br KMnO
79. A 2 4  B
 

Compound A and B respectively are:


(A) o-Bromostyrene, benzoic acid (B) p-Bromostyrene, benzaldehyde
(C) m-Bromostyrene, benzaldehyde (D) Styrene dibromide, benzoic acid
2 2CrO Cl 2 H O
80. C6H5CH3    A   B
The functional group present in B and name of the reaction would be
(A) –CHO, Gattermann aldehyde synthesis (B) –CHO, Etard reaction
(C) –COCH3, Friedel Crafts reaction (D) –CHO, Oxo reaction
O
Zn ( Hg ) 
81. +
AlCl
 SOCl
O 3    2  AlCl
3  Zn
(Hg )
 H/
KMnO 4
 P
HCl HCl 
O
P is
COOH
COOH
COOH CHO
(A) (B) (C) (D)
COOH COOH CHO
COOH

OH O
||
CH 3 C Cl
82. (
i ) OH
   
 P
(ii ) CO 2

(iii ) H 
P is a drug, it is

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O
OH O – C – CH3
O
C – CH3 OH
(A) (B)

COOCH3 COOH

(C) OH (D) O – C – CH3


O

(i ) O 
83. Na
/NH3
 3   NaOH  /
CaO
 J
( ii ) H O / H O
EtOH 2 2 2 
J is

(A) H3C – CH3 (B) CH4 (C) H3C–CH2–CH3 (D)

F
Cl NO2
 
NaOMe / 
84.   X , X is
NO2

F OMe Cl OMe
MeO NO2 F NO2 MeO NO2 Cl NO2

(A) (B) (C) (D)


NO2 NO2 NO2 NO2

85. The correct order of electrophilic aromatic substitution among the following:

O
CH3 O–C–CH3 OH NH2

(I) (II) (III) (IV)


(A) I > II > III > IV (B) IV > III > II > I (C) I > II > IV > III (D) III > IV > II > I


86. CH2 NO
2BF
4¯

O2N

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24 Physics
Chemistry
What is / are the product(s) in the reaction?

NO2
NO2

CH2 CH2
(A) (B)

O2N O2N

CH2 NO2
(C) (D) Both (B) and (C)
O 2N
87. Which of the following reaction(s) can produce aromatic hydrocarbon?
OH

(A) H3C – C  CH Re



d Hot
 (B) Zn
 /

Fe tube
H 3C CH3

SO3H MgBr

(C) H/
H 2O
 (D) H
2O


CH3

NH2

88.  conc
 .H N O
3 Product
H 2S O 4

Choose the correct statement(s):


(A) In the reaction, NO2 is the electrophile & it is electrophilic substitution.
(B) In the electrophilic substitution, nitration proceeds faster than that over benzene.
(C) In the electrophilic substitution, nitration proceeds slower than that over benzene.
(D) The reaction gives meta substitution product as the predominant product.

AlCl (i) O / 
89.
 Cl  CH 2CH 2  CH 3 3  P 
2
 Q  Phenol
( ii ) H 3O 
The major products P and Q are

(A) and CH3CH2CHO (B) and CH3COCH3

(C) and CH3COCH3 (D) and CH3CH2CHO

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Paragraph for Question Nos. 90 to 92
Riemer-Tiemann reaction introduces an aldehyde group, on to the aromatic ring of phenol, ortho to the hydroxyl
group. This reaction involves electrophilic aromatic substitution. This is a general method for the synthesis of
substituted salicylaldeydes as depicted below.

 [I]  aq


. HCl

(Intermediate)

90. Which one of the following reagents is used in the above reaction?
(A) aq. NaOH + CH3Cl (B) aq. NaOH + CH2Cl2
(C) aq. NaOH + CHCl3 (D) aq.NaOH + CCl4
91. The electrophile in this reaction is

(A)  CHCl (B) +CHCl2 (C)  CCl 2 (D)  CCl 3


92. The structure of the intermediate I is

(A) (B) (C) (D)

93. Major product of this reaction will be :

CH Cl
3
AlCl 3 ,

(A) o-xylene (B) p-xylene (C) Cumene (D) m-xylene

94.  ? Product is:




(A) (B)

(C) (D) no reaction

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26 Physics
Chemistry
Biomolecules, Polymer and Chemistry in Every Day Life

95. Which amino acid among following can not synthesised by Gabriel's pnthalimide synthesis method ?
(A) Glycine (B) Alanine (C) Proline (D) Phenylalaline
96. The non-essential amino acid among following is :
(A) Valine (B) Histidine (C) Proline (D) Leucine

97. The correct structure of prolin among at pH 3.0

98.

Compound formed in above reaction is :


(A) Alanine (B) Glycine (C) Phenyl alanine (D) None of these

99. Select incorrect match among following :

100. The pentose sugar in DNA and RNA has the :


(A) Open chain structure (B) Pyranose structure (C) Furanose structure (D) None of the above
101. Vitamin D is also called as :
(A) Ascorbic acid (B) Calciferol or ergocalciferol
(C) Thiamine (D) Riboflavin
102. Identify the vitamin whose deficiency in our food decreases reproductive power :
(A) vitamin A (B) vitamin C (C) vitamin D (D) vitamin E
103. Vitamin B6 is known as
(A) Pyridoxine (B) Thiamine (C) Tocopherol (D) Riboflavin

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HC N NH Ph
C N NH Ph
HO H
104. H OH The given osazone can be obtained by :
H OH
CH2OH

(A) D-glucose (B) D-mannose (C) D-Fructose (D) All of these


105. Complete hydrolysis of cellulose gives
(A) D-fructose (B) D-ribose (C) D-glucose (D) L-glucose
106. Nylon threads are made up of
(A) Polyvinyl polymer (B) Polyester polymer
(C) Polyamide polymer (D) Polyethylene polymer
107. Which of the following pairs give positive Tollen’s test ?
(A) Glucose, sucrose (B) Glucose, fructose
(C) Hexanal, Acetophenone (D) Fructose, sucrose
108. Protein is a polymer of:
(A) Glucose (B) Terephthalic acid (C) Amino acid (D) Glycol

109. Bakelite is obtained from


(A) Phenol and formaldehyde
(B) Adipic acid and hexamethylene diamine
(C) dimethyl terephthalate and ethylene glycol
(D) Neoprene

110. Adipic acid reacts with hexamethylene diamine to form


(A) Bakelite (B) Nylon-6,6 (C) Terylene (D) Nylon-6, 10
111. The drug that relieve or decrease pain is called
(A) Analgesic (B) Antipyretic (C) Tranquillizer (D) Hypnotics
112.. Streptomycin is an example of
(A) Antibiotic (B) Analgesic (C) Antipyretic (D) Anaesthetic.
113. Which of the following is Narcotic analgesics
(A) Morphine (B) Asprin (C) paracetamol (D) Equanil
114. Which of the following is used for the treatment of tuberculosis ?
(A) Veronal (B) Aspirin (C) Chloroquine (D) Streptomycin
115. Substances which bring body temperature down are known as:
(A) antipyretic (B) analgesics (C) antibiotics (D) hypnotics
116. The correct structure of DDT is :
Cl

(A) Cl CH – CCl3 (B) Cl C – CCl3

Cl Cl

Cl
(C) Cl C – CH2 Cl (D) H3C CH Cl
Cl CCl3

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28 Physics
Chemistry
117. The correct strutcure of Aspirin is :
OCOCH3 COCH3
(A) (B)
COOH COOH
OCOCH3
COCH3
(C) (D)
HOOC
OH
118. Peptide linkage is -
O O O O
(A) –C – O – (B) –C – NH2 (C) –C – NH– (D) –C – NH–NH2

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ANSWER KEY
1. D 2. B 3. B 4. D 5. A 6. CD 7. ABD
8. A 9. BD 10. (A)P,Q,R,S ; (B)P,Q,R,S ; (C)P,Q,S ; (D)P,Q,R,S 11. B
12. C 13. C 14. B 15. A 16. B 17. A 18. BCD
19. ACD 20. ACD 21. BCD 22. 9 23. 24
24. AP ; BR ; CS ; DQ 25. 1 26. C 27. C 28. B
29. A 30. A 31. A 32. C 33. AC 34. ABD 35. 2
36. D 37. C 38. D 39. D 40. D 41. A 42. B
43. B 44. D 45. AC 46. C 47. (A) Q (B) R (C) S 48. B
49. A 50. C 51. B 52. C 53. B 54. A 55. B
56. D 57. C 58. C 59. D 60. B 61. B
62. ABC 63. (A - q; B - p; C - s; D - r) 64. A 65. B 66. A 67. C
68. D 69. B 70. D 71. A 72. A 73. AD 74. B
75. A 76. B 77. 6 78. B 79. D 80. B 81. B
82. D 83. B 84. D 85. B 86. D 87. ABCD 88. AC
89. C 90. C 91. C 92. B 93. D 94. A 95. C
96. C 97. C 98. C 99. A 100. C 101. B 102. D
103. A 104. D 105. C 106. C 107. B 108. C 109. A
110. B 111. A 112. A 113. A 114. D 115. A 116. A
117. A 118. C

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