The effect that makes 2,3–dimethyl-2-butene more stable than 2-butene is-

1. Resonance

2. Hyperconjugation

3. Steric effect

4. Inductive effect

The IUPAC name of the above mentioned compound is - 

1. Cyclohexylidenemethanone

2. Cyclohexylidemethanone

3. Cyclohexylidenylmethanone

4. Cyclohexdenemethanone

Paper chromatography is an example of:

1. Partition chromatography

2. Thin layer chromatography

3. Column chromatography

4. Adsorption chromatography

A tertiary butyl carbocation is more stable than a secondary butyl carbocation because-

1. + R effect of ${CH}_3$ groups 

2. $-$R effect of $-$ CH₃  groups 

3. Hyperconjugation 

4. $-$l effect of $-$CH₃ groups 

The IUPAC name of the compound is :

1. 2,3 - Diemethylheptane

2. 3- Methyl -4- ethyloctane

3. 5-Ethyl -6-methyloctane

4. 4-Ethyl -3 - methyloctane.

Total number of stereoisomers of the compound:-

1. 10

2. 8

3. 6

4. 4

Which among these can exhibit tautomerism?

1. a only

2. b only

3. c only

4. a and c

In the reaction,

${\mathrm{CH}}_3\mathrm{CHO}+\mathrm{HCN}\to {\mathrm{CH}}_3\mathrm{CH}\left(\mathrm{OH}\right)\mathrm{CN}$

a chiral centre is produced. This product would be

1.  racemic mixture

2.  meso compound

3.  dextrorotatory

4.  laevorotatory

The compound that contains only sp³ hybridized carbon atoms is:

1.  HCOOH

2.  ${\left({\mathrm{NH}}_2\right)}_{2}CO$

3.  ${\left({\mathrm{CH}}_3\right)}_{3}COH$

4.  $C{H}_{\mathit{3}}CHO$

How many distinct products can be formed from the monochlorination of 2-methylbutane, excluding optical isomers?