The most stable carbocation among the following is-
1. \(({CH_3})_3C\overset{+}{C}H_2\)
2. \(({CH_3})_3\overset{+}{C}\)
3. \({CH_3}CH_2\overset{+}{C}H_2\)
4. \(({CH_3})\overset{+}{C}HCH_2CH_3\)
is more stable than because :
1. | NO2 shows +I effect |
2. | NO2 shows -I effect |
3. | NO2 decreases the positive charge on the compound |
4. | Ethyl group increases positive charge on the compound |
Alkyl groups act as electron donors when attached to a π system due to-
1. Inductive effect
2. Mesomeric effect
3. Resonance
4. Hyperconjugation
The effect that can explain the given order of acidity of the carboxylic acids is-
Cl3CCOOH > Cl2CHCOOH > ClCH2COOH
1. +I effect
2. -I effect
3. +E effect
4. -E effect