Which of the following carbocations is the mo | vedclass

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Question

(C) The correct option is $(C)$. In the benzyl carbocation $(C_6H_5CH_2^+)$,the positive charge on the carbon atom is delocalized over the benzene rin

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$C_6H_5CH_2^+$

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(C) The correct option is $(C)$. In the benzyl carbocation $(C_6H_5CH_2^+)$,the positive charge on the carbon atom is delocalized over the benzene ring through resonance. This resonance stabilization makes the benzyl carbocation significantly more stable than the primary alkyl carbocations ($CH_3CH_2^+$ and $CH_3CH_2CH_2^+$) and the methyl carbocation $(CH_3^+)$.

Which of the following carbocations is the most stable?

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