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(C) The stability of a carbocation is determined by the extent of resonance and inductive effects.$1$. $(CH_3)_3C^+$ is a tertiary alkyl carbocation s

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$(C_6H_5)_3C^+$

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(C) The stability of a carbocation is determined by the extent of resonance and inductive effects.$1$. $(CH_3)_3C^+$ is a tertiary alkyl carbocation stabilized by hyperconjugation and inductive effects.$2$. $C_6H_5CH_2^+$ is a benzyl carbocation stabilized by resonance with one phenyl ring.$3$. $(C_6H_5)_2CH^+$ is a benzhydryl carbocation stabilized by resonance with two phenyl rings.$4$. $(C_6H_5)_3C^+$ is a trityl carbocation stabilized by resonance with three phenyl rings.Since $(C_6H_5)_3C^+$ has the maximum number of phenyl rings,it exhibits the greatest degree of resonance stabilization,making it the most stable carbocation among the given options.

Which of the following compounds forms the most stable carbocation: $(CH_3)_3C-Br$,$(C_6H_5)_3CBr$,$(C_6H_5)_2CHBr$,and $C_6H_5CH_2Br$?

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