Single Choice Question: CH CH C CH CL C F C CH - Oh
Single Choice Question: CH CH C CH CL C F C CH - Oh
Single Choice Question: CH CH C CH CL C F C CH - Oh
CH2=Cl F CH2–OH
CH=CH2
C C C
(A) C (B) H C (C) HO (D) D
CH2–CH2–Cl CH3 OCH3
H CH3 3
OH NH2 T
COOH
2. The S-enantiomers of ibuprofen is reversible for its pain relieving properties. Which one of the structure
shown is S-ibuprofein?
(A) (B)
(C) (D)
4. (R)-2-chlorobutane is represented by :
(A) III and IV (B) I, III, and IV (C) I and IV (D) I and III
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6. Which structure represents (S)-1-chloro-1-fluoroethane ?
(A) I (B) II (C) III (D) More than one of the above
(A) I (B) II (C) III (D) More than one of the above
9. is properly named :
10. The Cahn-Ingold-Prelog stereochemical designations used for the following substance are :
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11. Which of these is not a correct Fischer projection formula of the (S) form of 3-bromo-1,1-dichloro-2-propanol?
CHCl2 CH2Br H OH
H OH HO H Cl2HC CH2Br H CHCl2
CH2Br CHCl2 OH CH2Br
(I) (II) (III) (IV)
CH2–CH3
CH2–CH3 SR CH2–CH3
H3C OPh
H3C I
(A) (B) H NR2 (C) (D)
CH3 Et CH2–CH2–CH3
13. Match the column-I with column-II, where column-I indicates a compound and column-II indicates its
configuration. Note that column-I may have more than one matching options in column-II.
Column-I Column-II
(A) (P) 2R 3S
(B) (Q) S
(C) (R) R
(D) (S) 2S 3R
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Integer Type Question
14. How many compounds having R configuraiton in the following given compounds.
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Answer Key + Solution
1. A 2. B 3. D 4. C 5. C
6. D 7. B 8. A 9. D 10. C
11. D
14. 4
Solution
1. A
2
CH=CH2
4 C 3 SR
H CH3
1COOH
2. B
3. D
Cl H Cl H
2 4
1 3 5
4. C
4
H
3 1
H3C Cl
2 CH CH3
2
(R-2-Chlorobutane)
5. C
4 4 3
H H CH3
1 1 3 1 4
3
(I) H3C OH (III) HO CH3 (IV) HO H
2 2 2
CH2CH3 CH2CH3 CH2CH3
R-2-butanol S-2-butanol R-2-butanol
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6. D
2 2 3
F F CH3
1 4 4 1 4 1
Cl H H Cl H Cl
3 CH3 3 CH3 2F
(I) = S (II) = R (III) = S
7. B
2 2 3
F F CH3
1 4 4 1 4 1
Cl H H Cl H Cl
3 CH3 3 CH3 2F
(I) = S (II) = R (III) = S
8. A
3
CH3
4 1
H Br S
2
CH2CH3
9. D
5 6
CH2CH3
3
4 4 1
H 1
Cl =S
2
4 3
3 (2S, 3R, 4S)-2,4-dichloro-3-methylhexane
H CH3 = R
2
1 2 4
Cl H =S
3
1 CH3
10. C
4
H 3 3
1
Cl
Cl 4 3 2 4 =R
R= 1 2 H (2R, 4R)
5 1 2
Cl
Cl
11. D
1
OH
4 3
H CHCl2
1 CH2Br
(R)
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12. BCD
1
SR
4 2
(B) H NR2 =S
3 Et
3
CH2–CH3
4 1
(C) H3C I =S
2
CH2–CH2–CH3
3
CH2–CH3
4 1
(D) H3C OPh =S
2
13. C
A-R ; B-Q ; C-P ; D - S
3
1 4
Sol. (A) NH2 CH = NH =R
2
CH2OH
4 5 1
1 1
(B) 3 6 =S
1
2 1
4
CH3
3
H Cl = S
(C) = 2R–3S
2
H Br = R
1CH3
1
COOH
2
HO H =S
(D) = 2S–3S
3
H OH = R
CH3
4
14. 4
Sol. (1) S (2) R (3) R (4) R (5) no chiral centre (6) S (7) R
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