Among the following,the most stable isomer is

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(D) The stability of cyclohexane derivatives is determined by the number of substituents in the equatorial position and the presence of intramolecular

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(D) The stability of cyclohexane derivatives is determined by the number of substituents in the equatorial position and the presence of intramolecular interactions like hydrogen bonding.In the case of $2$-methoxycyclohexanol,the isomer where both $-OH$ and $-OCH_3$ groups are in the axial positions (diaxial) allows for the formation of an intramolecular hydrogen bond between the $-OH$ hydrogen and the oxygen of the $-OCH_3$ group.This intramolecular hydrogen bonding stabilizes the diaxial conformation,making it more stable than the diequatorial or other conformations in this specific case.Therefore,the most stable isomer is the one with both groups in the axial position.

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