




Study with the several resources on Docsity
Earn points by helping other students or get them with a premium plan
Prepare for your exams
Study with the several resources on Docsity
Earn points to download
Earn points by helping other students or get them with a premium plan
These notes are from a highly trained teacher
Typology: Study notes
1 / 8
This page cannot be seen from the preview
Don't miss anything!





___________________________________________________________________________________________________________________________________
Single Correct Choice Type
Cl
Cl
(C) (D) All of these
CH 3 (C) CH 3 - C = CHD
CH 3
H 3 C
H 3 C CH - CH = CHCOOH
___________________________________________________________________________________________________________________________________
Cl COOH
CH
(C) E, Z (D) No stereoisomerism is possible
Cl
Cl Cl (B)
Cl Cl
Cl
Cl Cl
Cl
Cl
Cl
Cl
How many geometrical isomers are possible for the above compound? (A) 3 (B) 4 (C) 6 (D) 8
How many geometrical isomers are possible for the above compound? (A) 0 (B) 2 (C) 3 (D) 4
H
Choose the correct relation between 1 & 2? (A) 1 = 2 (B) 1 > 2
___________________________________________________________________________________________________________________________________
2 2 2 3
Which conformer of above compound is most stable across C 2 C 3 (A) staggered (B) eclipsed (partially) (C) gauche (D) fully eclipsed
H (^) CH 3
H
H 3 C H
H H H
H
H (^) CH 3
H
H H
H H H
H 3 C
H (^) CH 3
H (^) CH 3
H
H
H
H H
H
H
H (D)
H (^) CH 3
H (^) H
H
H 3 C
H
H H
H
H
H
Paragraph for Question Nos. 26 - 27
Read the paragraph carefully and answer the following questions: Conformational isomers are generated due to the free rotation about single bond. Due to torsional strain eclipsed form in less thermodynamically stable than staggered form. The gauche is specific conformer of staggered in which bulky groups are oriented closer to one another. Hence, generally gauche form is less stable than staggered form. But sometimes it is not true when hydrogen bonding is present
F
OH
H
H
H
H
(B)
F
H
H
OH
H
H
H
H H
H
H
H H
H OH
F
H
H H
H
H
H HF OH
___________________________________________________________________________________________________________________________________
CH (^3)
CH (^3)
D
H
H
D
(B)
CH (^3)
D
D
CH (^3)
H
H
CH 3 CH^3
H D H
D
CH 3
CH 3
H
H
H
H
Cl Cl
Br Br
Cl Cl
Br Br (A) (B) Relationship between above pair (A) & (B) is: (A) Enantiomer (B) Diastereomers (C) Identical (D) Structural isomer
Me H Me
Me H
Me
H Br Br
H
___________________________________________________________________________________________________________________________________
Cl
Br
Cl
Br
Cl Cl
Cl
Cl
Br Br
is:
Cl (A) 2 (B) 4 (C) 6 (D) 8
N - OH
N N
R R
R (^) OH
HO
(A) Chiral (B) C 3 axis of symmetry (C) Optically active (D) All of these
H 5 C (^6)
H H
C 6 H (^5) (B) C^ C
H
C 6 H 5 H
C 6 H (^5)
CH (^3)
C 2 H 5 C 3 H (^7)
CH 3 (D) C^ C
H
CH 3 H
CH 3
___________________________________________________________________________________________________________________________________
Cl
Cl
(C) (D) All of these
CH 3 (C) CH 3 - C = CHD
CH 3
H 3 C
H 3 C CH - CH = CHCOOH
Cl COOH
CH
(C) E, Z (D) No stereoisomerism is possible