The most stable conformation of the product of the following reaction is:

1.		2.
3.		4.

(Only one enantiomer is taken)
Which of the following statement is correct about A and B?
(a) A  and B are mixture of diastereomers
(b) A and B are mixture of enantiomers
(c) A and B are optically active
(d) B is racemic mixture

The molecule among the following that has the hybridization ${\mathrm{sp}}^2,\hspace{0.17em}{\mathrm{sp}}^2,\hspace{0.17em}\mathrm{sp},\; and\hspace{0.17em}\mathrm{sp}$ from left to right atoms is:

1. $\mathrm{HC}\equiv \mathrm{C}-\mathrm{C}\equiv \mathrm{H}$

2. ${\mathrm{CH}}_2=\mathrm{CH}-\mathrm{C}\equiv \mathrm{CH}$

3. ${\mathrm{CH}}_2=\mathrm{CH}-\mathrm{CH}={\mathrm{CH}}_2$ 

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

In the given hydrocarbon, 

The type/state of hybridization of carbons 1, 3, and 5 respectively are:

1. sp², sp, sp³

2. sp, sp³, sp²

3. sp, sp², sp³

4. sp³, sp², sp

An organic molecule necessarily shows optical activity if it:

1. Contains asymmetric carbon atoms

2. Is non-planar

3. Is non-superimposable on its mirror image

4. Is superimposable on its mirror image

The compound that has least hindered rotation around carbon-carbon bond is-

Which alkene among the following reacts the fastest with H₂​ under catalytic conditions?
 

1.		2.
3.		4.

A compound possessing optical isomerism provided it has the molecular formula C₇H₁₆, would be: