The R and S enantiomers of an optically active compound differ in:

1. Their optical rotation of plane-polarized light.

2. Their reactivity with chiral reagents.

3. Their solubility in achiral reagents.

4. Their melting points.

Subtopic:  Conformational Isomers |
 90%
From NCERT
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The most stable conformation of n-butane among the following is:

1. 2.
3. 4.
Subtopic:  Conformational Isomers |
 88%
From NCERT
AIPMT - 2010
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The pair of structures given below represent-
  

1. Enantiomers 2. Position isomers
3. Conformers 4. None of the above
Subtopic:  Conformational Isomers |
 64%
From NCERT
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