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
Which among these can exhibit tautomerism?
1. a only
2. b only
3. c only
4. a and c
A tertiary butyl carbocation is more stable than a secondary butyl carbocation because-
1. + R effect of 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.
The pair of structures that does not represent isomers is:
1. | ![]() |
2. | ![]() |
3. | ![]() |
4. | ![]() |
The presence of a halogen on the benzene ring in a nitration reaction leads to:
1. | Direct nitro group to come at meta and deactivate the ring due to –I effect of halogen. |
2. | Direct nitro group to come at ortho and para position and deactivate the ring due to –I effect of halogen. |
3. | Direct nitro group to come at meta and activate the ring toward nitration reaction. |
4. | Nitration reaction does not take place due to deactivation caused by –I effect of halogen. |
Which carbocation is the most stable among the options provided?
1. | 2. | ||
3. | 4. |