EASY
Earn 100

Resolution of racemic mixture is not used to separate the isomers present in racemic mixture.

50% studentsanswered this correctly

Important Questions on Organic Chemistry: Some Basic Principles and Techniques

HARD

For the given compound X, the total number of optically active stereoisomers is ____.

Question Image

MEDIUM
The number of chiral carbon centres in penicillin is _________.
HARD

The Fischer projection of D-erythrose is shown below.

Question Image 

D-Erythrose and its isomers are listed as P,Q,R, and S in Column I. Choose the correct relationship of P,Q,R, and S with D-erythrose from Column II.

  Column - I   Column -II
P. Question Image 1. Diastereomer
Q. Question Image 2. Identical
R. Question Image 3. Enantiomer
S. Question Image    

 

 

HARD
Which of the following compounds will show the maximum 'enol' content?
EASY
The number of chiral carbons in chloramphenicol is ____________.
MEDIUM
Which one of the following compounds is optically active?
MEDIUM
Which among the given molecules can exhibit tautomerism ?

Question Image
MEDIUM
(+) 2-Methylbutan-1-ol and (-) 2- Methylbutan-1-ol have different values for which property?
EASY
The correct statement regarding a carbonyl compound with a hydrogen atom on its alpha carbon, is:
EASY
Which of the following acids does not exhibit optical isomerism?
HARD
Total number of isomers, considering both structural and stereoisomers, of cyclic ethers with the molecular formula C4H8O is ________
MEDIUM

Which of the following carbonyl compounds will exhibit enolization?

(i) Question Image

(ii)Question Image

(iii) Question Image

(iv) Question Image

(v) Question Image

MEDIUM

The absolute configurations of the following compounds Question Image respectively, are

EASY

The correct statement about the following compounds

Question Imageis

EASY
In assigning R-S configuration which among the following groups has highest priority?
MEDIUM
The optically inactive compound from the following is:
MEDIUM
Among the following, the conformation that corresponds to the most stable conformation of meso-butane-2,3-diol is