Among the following,the most stable compound | vedclass

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(D) The stability of substituted cyclohexanes depends on steric hindrance and intramolecular interactions. In $1,2-$cyclohexanediol,the $OH$ groups ar

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$trans-1,3-$cyclohexanediol

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(D) The stability of substituted cyclohexanes depends on steric hindrance and intramolecular interactions. In $1,2-$cyclohexanediol,the $OH$ groups are closer,leading to higher steric repulsion. In $1,3-$cyclohexanediol,the $OH$ groups are further apart,reducing steric repulsion. Between $cis$ and $trans$ isomers,the $trans-1,3-$cyclohexanediol allows both $OH$ groups to occupy equatorial positions in the chair conformation,which significantly minimizes steric strain compared to other isomers. Therefore,$trans-1,3-$cyclohexanediol is the most stable compound.

Among the following,the most stable compound is:

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