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Single Choice Question: CH CH C CH CL C F C CH - Oh

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Single Choice Question

1. Indicate the structure/s having R configuration.

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)

3. Which of the following molecules is achiral ?


(A) (2R, 3R)-2,3-dichloropentane (B) (2R, 3S)-2,3-dichloropentane
(C) (2S, 4S)-2,4-dichloropentane (D) (2S, 4R)-2,4-dichloropentane

4. (R)-2-chlorobutane is represented by :

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

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

5. Which of the following represent (R)-2-butanol ?

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

(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

7. Which structure represent (R)-1-chloro-1-fluoroethane ?

(A) I (B) II (C) III (D) More than one of the above

8. Which structure represents (S)-2-bromobutane ?

(A) I (B) II (C) III (D) None of the above

9. is properly named :

(A) (3R, 4S, 5R)-3,5-dichloro-4-methylhexane


(B) (2S, 3S, 4S)-2,4-dichloro-3-methylhexane
(C) (2S, 3R, 4R)-2,4-dichloro-4-methylhexane
(D) (2S, 3R, 4S)-2,4-dichloro-3-methylhexane

10. The Cahn-Ingold-Prelog stereochemical designations used for the following substance are :

(A) 2R, 4S (B) 2S, 4R (C) 2R, 4R (D) 2S, 4S

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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)

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

One or more than one Type Question

12. Indicate figure/s having S configuration.

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

(A) A-Q ; B-R ; C-P ; D - S


(B) A-S ; B-R ; C-P ; D - S
(C) A-R ; B-Q ; C-P ; D - S
(D) A-S ; B-P ; C-R ; D - Q

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Integer Type Question

14. How many compounds having R configuraiton in the following given compounds.

(1) (2) (3) (4)

(5) (6) (7)

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Answer Key + Solution

Single Choice Question

1. A 2. B 3. D 4. C 5. C
6. D 7. B 8. A 9. D 10. C
11. D

One or more than one Type Question

12. BCD 13. C

Integer Type Question

14. 4

Solution

1. A

2
CH=CH2
4 C 3 SR
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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