Ethers react with HI to form two cleavage products. One of the products might react further with HI. In the

Provide the product. Reagent: Excess HI

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Why did the cleavage occur at the O-C to the ethyl? In the reaction below,I understand that it did at that specific O-C bond because methyl carbocations are more stable than phenyl's.

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organic chemistry - Acidic cleavage of ether with a 2° alkyl group - Chemistry Stack Exchange

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