Which of the following carbocations is expect | vedclass

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(B) The stability of a carbocation is determined by resonance and inductive effects. In the given structures,the carbocation in option $B$ is a tertia

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(B) The stability of a carbocation is determined by resonance and inductive effects. In the given structures,the carbocation in option $B$ is a tertiary allylic carbocation where the positive charge is stabilized by resonance with two double bonds and the electron-donating inductive effect of the $CH_3$ group. Specifically,the positive charge is located at the carbon atom directly attached to the $CH_3$ group,which provides maximum stabilization through hyperconjugation and resonance. Therefore,the carbocation in option $B$ is the most stable.

Which of the following carbocations is expected to be most stable?

Similar Questions

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$III. CH_3CH_2CH_2CH_2^{\oplus}$
$IV. CH_3CH^{\oplus}CH_2CH_3$

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