What is the correct order of stability for 1^ | vedclass

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Question

(B) The stability of carbocations is determined by inductive effect,hyperconjugation,and resonance. $3^\circ$ carbocations are stabilized by hyperconj

Vedclass · Accepted Answer

$	ext{benzyl} > 3^\circ > 2^\circ > 1^\circ$

Vedclass · Answer

(B) The stability of carbocations is determined by inductive effect,hyperconjugation,and resonance. $3^\circ$ carbocations are stabilized by hyperconjugation and inductive effects of three alkyl groups. Benzyl carbocation $(C_6H_5CH_2^+)$ is stabilized by resonance with the benzene ring. Resonance stabilization is generally more effective than the hyperconjugation and inductive effects present in $3^\circ$ alkyl carbocations. Therefore,the order of stability is: $	ext{benzyl} > 3^\circ > 2^\circ > 1^\circ$.

What is the correct order of stability for $1^\circ, 2^\circ, 3^\circ$ carbocations and benzyl carbocation?

Similar Questions

Consider the following carbocations:
$I. C_6H_5CH_2^+$
$II. CH_2=CH^+$
$III. CH_3-CH^+(CH_3)$
$IV. CH_3-CH_2^+$
$V. HC \equiv C^+$
Arrange the above carbocations in the order of decreasing stability.

Which is the most stable carbocation?

Which of the following bridgehead carbocations is the most stable?

The bond dissociation energy of the $C-H$ bond for the compounds: $(I)\ CH_3-H, (II)\ CH_3-CH_2-H, (III)\ CH_2=CH-CH_2-H, (IV)\ C_6H_5-H$ follows the order:

The following carbocation is stabilized by the interaction of the empty $p$ orbital with:

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