Which among the following halides will genera | vedclass

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(D) The stability of a carbocation is determined by resonance,hyperconjugation,and the inductive effect. In the given options,the carbocations formed

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$(C_6H_5)_3C-Br$

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(D) The stability of a carbocation is determined by resonance,hyperconjugation,and the inductive effect. In the given options,the carbocations formed are: $A$: Allyl carbocation $(CH_2=CH-CH_2^+)$ $B$: Benzyl carbocation $(C_6H_5-CH_2^+)$ $C$: Cyclohexenyl carbocation $D$: Triphenylmethyl carbocation $((C_6H_5)_3C^+)$ Among these,the triphenylmethyl carbocation is the most stable because the positive charge is delocalized over three phenyl rings through extensive resonance. Therefore,$(C_6H_5)_3C-Br$ generates the most stable carbocation.

Which among the following halides will generate the most stable carbocation in a nucleophilic substitution reaction?

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