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(D) The hydrolysis of the corresponding halide precursor in the presence of acetone typically proceeds via an $S_N1$ mechanism. In this specific react

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$K$ and $M$

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(D) The hydrolysis of the corresponding halide precursor in the presence of acetone typically proceeds via an $S_N1$ mechanism. In this specific reaction,the carbocation intermediate formed is stabilized by the electron-donating $p$-methoxy group. The stereochemistry of the product depends on the attack of the nucleophile on the planar carbocation. Given the structures provided,the reaction leads to the formation of both $K$ and $M$ as diastereomeric products due to the lack of stereospecificity in the $S_N1$ pathway.

What is obtained by hydrolysis in the presence of acetone?

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