The most stable chair conformation of cis-1-tert-butyl-3-chlorocyclohexane places the bulky tert-butyl group in an equatorial position while the smaller chlorine atom is placed axially, thereby reducing steric strain. This configuration maximizes stability in the molecular structure. Drawing the chair conformation accurately shows the positioning of these two groups for optimal stability. ;
The most stable chair conformation of cis-1-tert-butyl-3-chlorocyclohexane has the bulky tert-butyl group in an equatorial position and the smaller chlorine atom in an axial position. This arrangement minimizes steric strain, resulting in maximum stability. Properly positioning the groups allows for optimal balance and stability in the molecular structure.
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