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Important Instructions:

1. Immediately fill in the particulars on this page of the Test Booklet with Blue or Black Ball Point Pen.
To mark answers on the OMR Sheet, use Blue or Black ball point pen only.
2. The Test Booklet consists of 180 questions. There are three sections in the question paper, Subject I, II and
III consisting of Physics (45 Questions), Chemistry (45 Questions), Botany (45 questions) & Zoology (45
questions) in each subject of equal weightage.
3. Each question is allotted 4 (four) marks for correct response. For each wrong answer, 1 (One) mark will be
deducted. No deduction from the total score will be made if no response is indicated for an item in the
answer sheet.
4. There is only one correct response for each question. Filling up more than one response in any question
will be treated as wrong response and marks for wrong response will be deducted accordingly as per
instruction 3 above.
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device, etc. inside the examination room/hall.
6. Do not fold or make any stray mark on the Answer Sheet.
7. The candidates are governed by all Rules and Regulations of the Examination body with regard to their
conduct in the Examination Hall. All cases of unfair means will be dealt with as per Rules and Regulations
of the Examination body.

SUBJECT SYLLABUS COVERED


PHYSICS Thermodynamics and Kinetic theory of gases, Waves and Oscillations

CHEMISTRY GOC- (I, II & III), Hydrocarbons, Environmental Chemistry

BOTANY Sexual reproduction in flowering plants, Principles of Inheritance and variation

ZOOLOGY Neural Control and Coordination, Chemical coordination and integration


Vidyamandir Classes
SECTION - II (CHEMISTRY) 180 MARKS
46. An alkene on treating with hot acidified 52. The addition of Br2 to trans-2-butene produces:
KMnO 4 gives succinic acid. The alkene is: (1) (+)-2, 3-Dibromobutane
I (1) 1-Butene (2) 2-Butene (2) (–)-2, 3-Dibromobutane
(3) 2-methylbutene (3) rac-2,3-Dibromobutane
(4) Cyclobutene (4) meso-2, 3-Dibromobutane
47. Maleic acid is allowed to react with Br2 in 53. 2-Butyne is treated with sodium in liquid NH 3 .
CCl 4 . The product formed is: The major product formed is:
(1) Dibromotartaric acid (1) cis-2-Butene (2) trans-2-Butene
(2) Dibromosuccinic acid (3) Butane (4) 1, 3-Butadiene
(3) (  ) Dibromosuccinic acid 54. In the following reaction
(4) meso-Dibromosuccinic acid C 2 H 2 2H O
 X ƒ CH3CHO
HgSO /H SO
4 2 4
48. The addition of HBr to an alkene in the
What is X?
presence of peroxide is the example of:
(1) CH 3CH 2 OH
11 (1) Electrophilic addition reaction
(2) Nucleophilic addition reaction (2) CH 2  CHOH
(3) Free radical addition reaction (3) CH 3 CH 2 CHO
(4) The formation of carbocation as an (4) CH 3  O  CH 3
intermediate Electrophilic substitution
reaction 55. In the reaction,
49. 2-Butene on reductive ozonolysis will give: (i) X
(1) Acetaldehyde CH3C  C  CH3 
(ii) Zn/H O

2
(2) Acetic Acid H 3C  C  C  CH3
(3) Mixture of acetaldehyde and acetic acid
(2 : 1 ratio)
I || ||
O O
X is:

(4) Mixture of acetaldehyde and acetic acid (1) HNO 3 (2) O2


(1 : 2 ratio) (3) O3 (4) KMnO 4
50. Which among the following alkenes will be 56. What is the product formed when acetylene
most stable? reacts with hypochlorous acid?
(1) Ethene (2) 2-Methylpropene (1) CH 3COCl
(3) 2, 3-Dimethyl-2-butene
(4) 2-Butene I (2) ClCH 2 CHO
(3) Cl  CHCHO
51. The addition of HCl to 3, 3, 3-trichloropropene
(4) ClCH 2 COOH
give:
(1) Cl3CCH 2 CH 2 Cl 57. Which of the following is the most reactive
towards ring nitration?
I (2) Cl3CCH (Cl)CH 3
(1) Benzene (2) Mesitylene
(3) Cl2 CHCH (Cl)CH 2 Cl 1
(3) Toluene (4) m-Xylene
(4) Cl2 CHCH 2 CHCl 2

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Vidyamandir Classes
58. 1, 3-Butadiene when treated at low temperature CH CO H H
63. 
3 3
 

with Br2 gives: H 2O

(1) 1, 4-dibromo-2-butene
I (2) 1, 3-dibromo-2-butene (1)
(3) 3, 4-dibromo-1-butene
(4) 2, 3-dibromo-2-butene I
59. The most reactive compound for electrophilic (2)
nitration is:
(3) Both of these
(1) Benzene
(4) None of these
(2) Nitrobenzene
H O
(3) Benzoic acid 64. A 2
H SO ,HgSO

2 4 4
(4) Toluene
60. What would be the product formed when 1-
Bromo-3-Chlorocyclubutane reacts with two
Identify A and B respectively:
equivalents of metallic sodium in water? I (1) Acetone, propanal
II (2) Acetone, acetone
(3) Propanal, propanal
(1) (2)
(4) Propanal, acetone
(3) (4)
(1)OsO
65.  4

61. The reagent(s) for the following compounds (2) NaHSO 4

is/are:
(1) alcoholic KOH
(2) Alcoholic KOH followed by NaNH 2 (1) (2)
(3) Aqueous KOH followed by NaNH2
(4) Zn /CH 2 OH

CH 2 (3) (4)
Br2
62. | 
aq.NaOH

CH 2
Which of the following is not the expected 66. Which of the following reacts fastest with HCl?
product in the above reaction?
CH 2 Br CH 2Cl (1) (2)
(1) | (2) |
CH 2 Br CH 2Cl II
CH 2 Br CH 2 Br (3) (4)
(3) | (4) |
CH 2 Cl CH 2OH

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Vidyamandir Classes
67. The IUPAC name of: (1) 4 and 4 (2) 2 and 2
(3) 2 and 4 (4) 4 and 2
71. Maximum enolization take place of:
(1) CH 3COCH 3
(1) 3, 4-dimethyl pentanoyl chloride
10 (2) 1-chloro-1-oxo-2, 3-dimethyl pentane
(2) CH 3COCH 2 CHO
(3) 2-ethyl-3-methylbutanoylchloride 10 (3) CH 3COCH 2 COCH 3
(4) 2, 3-dimethyl pentanoyl chloride
68. (2R, 3R) – 2, 3-butanediol is: (4)

72. Tautomerism is not exhibited by:


(1)

(1)

(2)
10
(2)

(3)
(3)

(4)
(4)
69. Number of stereo isomers of tartaric acid
CH(OH)COOH
| 73. Number of optical isomers of X will be:
CH(OH)COOH
10 is: I
(1) 2 (2) 3
(3) 4 (4) 5 (1) 2 (2) 3
70. The compound, whose stereo-chemical formula (3) 4 (4) None of these
is written below, exhibits x geometrical isomers 74. Meso-tartaric acid is optically inactive due to:
and y optical isomers. ‘x’ and ‘y’ respectively (1) Two asymmetric carbon atom
are: (2) External compensation
10 10 (3) Molecular symmetry
(4) Molecular Asymmetry

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Vidyamandir Classes
75. Maleic acid and fumaric acid are: 80. Most stable alkene is:
(1) Position Isomers (1) CH 3CH  CHCH 3
(2) Functional Isomers
10 (3) Geometrical isomers
(4) Metamers (2)

76. Molecular formula C 4 H 9 NH 2 shows how


many isomers of primary amine:
(3)
10 (1) 2 (2) 3
(3) 4 (4) 5
77. The chirality of the compound is: (4)

81. Relative stabilities of the following carbocation


will be in order:

(1) R (2) S
(3) Z (4) E
10

78. Electrophile N O 2 attacks the following

(1) I  II  III  IV
(2) IV  II  III  I
(3) I  II  III  I
II (4) II  IV  III  I
82. Dehydrobromination (—HBr) of the following

In which case N O 2 will be at meta position: in increasing order is:

(1) II, IV (2) I, II, III


(3) II, III (4) I only
79. Among the following compounds the
decreasing order of reactivity towards
I (1) I  II  III (2) III  II  I
(3) I =II  III (4) III  I = II
electrophilic substitution is:

83.
II Which is correct statement?
(1) II  I  III  IV (1) A is formed by anti-addition and is Meso
(2) A is formed by syn-addition and is Meso
(2) III  I  II  IV
(3) A is formed by anti-addition and is
(3) IV  I  II  III
racemic
(4) I  II  III  IV (4) A is formed by syn-addition and is
racemic

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Vidyamandir Classes
84. Arrange the following in increasing acid (3) Mixture of both (1) & (2)
strength: (4) None of these
87. In Victor Meyer’s method 0.2 gm of an organic
substance displaced 56 ml of air at STP the
molecular weight of the compound:
(1) 56 (2) 112
(3) 80 (4) 28
10 (1) II  I  III  IV 88. The ammonia evolved from the treatment of
(2) II  I  IV  III 0.30 g of an organic compound for the
estimation of nitrogen was passed in 100 mL of
(3) III  IV  II  I
0.1 M sulphuric acid. The excess of acid
(4) IV  III  I  II
required 20 mL of 0.5 M sodium hydroxide
85. Most stable free radical is: solution for complete neutralization. The
10
organic compound is:
(1) Urea
(1) (2) (2) Benzamide
(3) Acetamide
10
(4) Thiourea
89. How much sulphur is present in organic
(3) compound if on analysis 0.53 gm of this
(4) None of these compound gives 1.158 gm of BaSO 4 ?
10 (1) 10% (2) 15%
86. Product (s) of the following S N 1 reaction is/are:
(3) 20% (4) 30%
90. Which of these gases is not considered to be an
air pollutant?
(1) R-butan-2-ol (1) NO 2 (2) SO 2
(2) S-butan-2-ol (3) O3 (4) CO

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Vidyamandir Classes

    End of (VPTS-3B) PRACTICE TEST SERIES-3B | NEET-2021    


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