(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.