In the following reaction,the major products | vedclass

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(C) The reaction of benzyl phenyl ether with $HI$ proceeds via the protonation of the ether oxygen atom. Following protonation,the bond between the ox

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(C) The reaction of benzyl phenyl ether with $HI$ proceeds via the protonation of the ether oxygen atom. Following protonation,the bond between the oxygen and the benzylic carbon breaks to form a stable benzylic carbocation $(C_6H_5CH_2^+)$ and phenol $(C_6H_5OH)$. The benzylic carbocation is resonance-stabilized. Finally,the iodide ion $(I^-)$ attacks the benzylic carbocation to form benzyl iodide $(C_6H_5CH_2I)$. Thus,the major products are benzyl iodide and phenol. This corresponds to option $C$.

In the following reaction,the major products are

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