The correct order of stability of the followi | vedclass

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Question

(A) The stability of carbocations is determined by the presence of electron-donating groups attached to the positively charged carbon atom. $(a)$ $(CH

Vedclass · Accepted Answer

$a > d > b > c$

Vedclass · Answer

(A) The stability of carbocations is determined by the presence of electron-donating groups attached to the positively charged carbon atom. $(a)$ $(CH_3)_2C^+-NHCH_3$: The nitrogen atom has a lone pair which provides strong resonance stabilization ($+M$ effect) to the carbocation. $(d)$ $(CH_3)_2C^+-OCH_3$: The oxygen atom has lone pairs which provide resonance stabilization ($+M$ effect). Since nitrogen is less electronegative than oxygen,it donates its lone pair more effectively,making $(a)$ more stable than $(d)$. $(b)$ $(CH_3)_2C^+-CH_2CH_3$: This is a tertiary carbocation stabilized by the inductive effect $(+I)$ and hyperconjugation of the alkyl groups. $(c)$ $(CH_3)_2CH^+$: This is a secondary carbocation,which is less stable than the tertiary carbocation $(b)$. Thus,the order of stability is $(a) > (d) > (b) > (c)$.

The correct order of stability of the following carbocations is:

Similar Questions

Which of the following carbocations is most stable?
$A) (CH_3)_2CH-CH^+-CH_3$
$B) (CH_3)_2C^+-CH_2CH_3$

The order of circled $C-H$ bond dissociation energy in the following compounds is:

Among the given species,which carbocations are resonance stabilized?

Which free radical structure will show the maximum resonance? (Given: $\phi = C_6H_5$)

Which of the following carbocations is expected to be most stable?

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