Advertisements
Advertisements
Question
Which of the following carbocation will be most stable?
Options
Ph3+C –
CH3 – +CH2 –
(CH3)2 – +CH
CH2 = CH – +CH2
Solution
CH2 = CH – +CH2
APPEARS IN
RELATED QUESTIONS
For the following reactions
- \[\ce{CH3CH2CH2Br + KOH → CH3 – CH = CH2 + KBr + H2O}\]
- \[\ce{(CH3)3CBr + KOH → (CH3)3COH + KBr}\]
Which of the following statement is correct?
Decreasing order of nucleophilicity is ______.
Which of the following species is not electrophilic in nature?
- I effect is shown by ______.
Assertion: Tertiary Carbocations are generally formed more easily than primary Carbocations ions.
Reason: Hyper conjucation as well as inductive effect due to additional alkyl group stabilize tertiary carbonium ions.
Heterolytic fission of C–C bond results in the formation of ______.
Write a short note on resonance.
Write a short note on hyperconjucation.
What is nucleophiles? Give a suitable example.
Explain the electromeric effect.