The most stable conformation of trans-1-tert-butyl-3-methylcyclohexane is the one in which:

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Quizplus · Accepted Answer

In cyclohexane, axial positions are less stable than equatorial positions due to steric hindrance between the substituent and neighboring axial hydrogen atoms. Therefore, the more stable conformation of trans-1-tert-butyl-3-methylcyclohexane is the one in which the bulky tert-butyl group is equatorial and the smaller methyl group is axial. This minimizes steric hindrance and maximizes stability.

The Most Stable Conformation of Trans-1-Tert-Butyl-3-Methylcyclohexane Is the One in Which