Which of the following is the most stabilized | vedclass

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(D) The stability of a carbocation $(C^{\oplus})$ is directly proportional to the extent of conjugation and resonance stabilization. In option $(d)$,t

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(D) The stability of a carbocation $(C^{\oplus})$ is directly proportional to the extent of conjugation and resonance stabilization. In option $(d)$,the positive charge is in conjugation with two double bonds,which provides extensive delocalization of the positive charge,making it the most stable carbocation among the given options.

Which of the following is the most stabilized carbocation?

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