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(D) The reactivity of a compound toward $S_N1$ reaction depends on the stability of the carbocation intermediate formed after the departure of the lea

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(D) The reactivity of a compound toward $S_N1$ reaction depends on the stability of the carbocation intermediate formed after the departure of the leaving group (in this case,$I^-$).Option $D$ shows a compound that,upon losing the $I^-$ ion,forms a carbocation that is stabilized by resonance,leading to an aromatic tropylium-like cation structure.Since the formation of an aromatic carbocation is highly favorable,the compound in option $D$ is the most reactive toward $S_N1$ reactions.

Most reactive compound toward $S_N1$ is

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