Isomers which can be interconverted through rotation around a single bond are:

1. Conformers             

2. Diastereomers

3. Enantiomers             

4. Positional isomers

How many structures of F are possible?

(1) 2

(2) 5

(3) 6

(4) 3

The optically active alkane with lowest molar mass is:

1. ${\mathrm{CH}}_3{\mathrm{CH}}_2\mathrm{C}\equiv \mathrm{CH}$

2. ${\mathrm{CH}}_3{\mathrm{CH}}_2-\stackrel{{\mathrm{CH}}_3}{\stackrel{|}{\mathrm{CH}}}-{\mathrm{CH}}_3$

3. 

4. ${\mathrm{CH}}_3{\mathrm{CH}}_2.{\mathrm{CH}}_2{\mathrm{CH}}_3$

a-D-(+)-glucose and β-D-(+)-glucose are :

(1) enantiomers

(2) conformers

(3) epimers

(4) anomers

The absolute configuration of 

 is:

(1) S, R                 

(2) S, S

(3) R, R                 

(4) R, S

The correct statement regarding electrophile is

With respect to the conformers of ethane, which of the following statements is true?

(1) Bond angle remains same but bond length changes

(2) Bond angle changes but bond length remains same

(3) Both bond angle and bond length change

(4) Both bond angles and bond length remain same

The IUPAC name of the compound

is-

1. 3-Keto-2-methylhex-4-enal

2. 5-Formylhex-2-en-3-one

3. 5-Methyl-4-oxohex-2-en-5-al

4. 3-Keto-2-methylhex-5-enal

The correct order of acidity among the following is:

1. CH₂=CH₂ >CH≡CH > CH₃C≡CH > CH₃-CH₃

2. CH≡CH > CH₃-C≡CH > CH₂=CH₂ >CH₃-CH₃

3. CH≡CH > CH₂=CH₂ > CH₃-C≡CH > CH₃-CH₃

4. CH₃-CH₃ > CH₂=CH₂ > CH₃-C≡CH > CH≡CH

The most suitable method of separation of 1:1 mixture of ortho and para-nitrophenols is

1. sublimation

2. chromatography

3. crystallisation

4. steam distillation