Practice Test 02 Chemistry
Practice Test 02 Chemistry
Practice Test 02 Chemistry
YAKEEN-2.0
Test-02 (Chemistry) 24-10-2021
46. The IUPAC name of the compound 50. The IUPAC name of the compound
CH3 CH3
HO
CH3
CH3CH2CH2CH CH CH2CH3
C CH2CH3 is is
CH
OH OH
(A) 1, 1 – dimethyl – 1, 3 – butanendiol Cl
(B) 2 – methyl – 2, 4 – pentane diol (A) 2-chloro-4-(N-ethyl) pentanone acid
(C) 1, 3, 3 – trimethyl – 1, 3 – propane diol (B) 2-chloro-3- (N, N-diethyl amino)
(D) 4 – methyl – 2, 4 – pentane diol propanoic acid
(C) 2-chloro-2-oxo diethyl amine
(D) 2-chloro-2-carboxy-N-ethyl ethane
2
66. Numbers of possible isomers of glucose are 73. Which type of isomerism is observed between
(A) 10 I and II.
(B) 14 I. CH3–CH2–NH–CHO
(C) 16 II. CH3C – CH – CHO
(D) 20 |
NH2
67. Draw all structurally isomeric alkenes with (A) Chain isomers
molecular formula C4H8. (B) Position isomers
(A) 3 (C) Functional isomers
(B) 4 (D) Metamers
(C) 5
(D) 6 74. How many positional isomers are possible for
dimethylcyclohexane?
68. Draw all structurally isomeric 2º chlorides (A) 3
with molecular formula C5H11Cl (B) 4
(A) 7 (C) 5
(B) 3 (D) 6
(C) 2
(D) 6 75. How many structural isomers of all the tertiary
alcohols with molecular formula C6H14O.
69. How many structurally isomeric benzene can (A) 2 (B) 3
be formed by molecular formula C7H8O (C) 4 (D) 5
(A) 9
(B) 4 76. Number of structurally isomeric ethers with
(C) 8 molecular formula C5H12O.
(D) 5 (A) 4 (B) 5
(C) 6 (D) 7
70. How many structurally isomeric cyclic
bromides can be formed having molecular 77. What is the number of all (structurally
formula C4H7Br isomeric) alkynes with molecular formula
(A) 5 C6H10.
(B) 4 (A) 6 (B) 7
(C) 8 (C) 8 (D) 9
(D) 3
78. Which one of the compound is not isomer of
71. Isomers have essentially identical others?
(A) Structural formula
(B) Chemical properties (A)
(C) Molecular formula
(D) Physical properties
(C)
(A) Chain isomers
(B) Position isomers
(C) Functional isomers
(D)
(D) Identical
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79. Which of the following compounds has wrong 82. Which one of the following pair represents
IUPAC name stereo isomerism
(A) CH3 – CH2 – CH2 – COO – CH2CH3 (A) Linkage isomerism and Geometrical
→ Ethyl butanoate isomerism
(B) (B) Chain isomerism and Rotational
isomerism
(C) Optical isomerism and Geometrical
→ 3-Methylbutanal isomerism
(C) (D) Structural isomerism and Geometrical
isomerism
→ 2-Methyl-3-butanol
83. Which of the following is not chiral?
(D) (A) 2–Butanol
(B) 2, 3–Dibromo pentane
(C) 3–Bromo pentane
→ 2-Methyl-3-pentanone (D) 2–Hydroxy propanoic acid
80. Which of the following pairs of compounds are 84. Among the following which one can have a
enantiomers meso form?
CH3 CH3
(A) CH3CH(OH)CH(CI)C2H5
H OH HO H (B) CH3CH(OH)CH(OH)CH3
(A) OH H and H OH (C) C2H5CH(OH)CH(OH)CH3
(D) HOCH2CH(CI)CH3
CH3 CH3
CH3 CH3 85. CH3–CHCI–CH2–CH3 has a chiral centre
H OH HO H which one of the following represents its R
(B) HO H
and H configuration
HO
C2H5 C2H5
CH3 CH3 | |
CH3 (A) H — C — CH3 (B) CI — C — CH3
| |
H OH CI H
(C) and OH CH3 C2H5
H | |
CH3 (C) H — C — CI (D) H3C — C — CI
| |
CH3 CH3 C2H5 H
HO H HO H
(D) OH
and H 86. In the following the most stable conformation
H HO
of n-butane is
CH3 CH3
(A) E (B) R
(B)
(C) S (D) Z
5
CH3
(C) H OH
CH3 OH
H
(A) 2S, 3S (B) 2S, 3R
(C) 2R, 3S (D) 2R, 3R
(D)
89. Which of the following compound is expected
to be optically active?
(A) (CH3)2 CHCHO
87. The geometrical isomerism is shown by (B) CH3CH2CH2CHO
CH2
CH2 (C) CH3CH2CHBrCHO
(A) (B) (D) CH3CH2CBr2CHO
Answer Key
46. (B)
47. (B)
48. (A)
49. (B)
50. (C)
51. (C)
52. (C)
53. (C)
54. (B)
55. (A)
56. (A)
57. (D)
58. (C)
59. (C)
60. (D)
61. (B)
62. (A)
63. (C)
64. (B)
65. (B)
66. (C)
67. (A)
68. (B)
69. (D)
70. (B)
71. (C)
72. (A)
73. (C)
74. (B)
75. (B)
76. (C)
77. (B)
78. (D)
79. (C)
80. (A)
81. (B)
82. (C)
83. (C)
84. (B)
85. (B)
86. (A)
87. (D)
88. (A)
89. (C)
90. (C)
7
50. (C)
51. (C)
53. (C)
54. (B)
55. (A)
70. (B)
56. (A)
57. (D)
58. (C)
73. (C)
62. (A)
63. (C)
64. (B)
65. (B)
66. (C)
Glucose has four dissimilar asymmetric
carbon atoms; a = 24.
Hence, (C) is the correct answer.
8
87. (D)
meso form
88. (A)
89. (C)
'R' configuration