Which of the following compounds is most stab | vedclass

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(D) The stability of substituted cyclohexanes depends on the orientation of the substituents. Substituents in the equatorial $(e)$ position are more s

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(D) The stability of substituted cyclohexanes depends on the orientation of the substituents. Substituents in the equatorial $(e)$ position are more stable than those in the axial $(a)$ position due to reduced $1,3$-diaxial interactions (steric repulsion).For $1,4$-dimethylcyclohexane,the $trans$ isomer can adopt a conformation where both methyl groups are in the equatorial position $(e, e)$.This $trans$-$1,4$-dimethylcyclohexane $(e, e)$ conformation is the most stable as it minimizes steric repulsion compared to the $cis$ isomer (which must be $a, e$) or other axial-containing conformations.

Which of the following compounds is most stable?

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