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The conformation with the bromine in the equatorial position is more stable because there is less steric hindrance between the halogen and the ring. Draw the most stable chair conformation for the following molecules: trans-1,2-dimethylcyclohexane trans-1-isopropyl-3-methylcyclohexane Consider the following molecule.  Which of the labeled bonds in the structure are equatorial bonds? a, d Which of the labeled bonds is trans to bond b? e Which bonds have a 1,3-diaxial interaction with each other? b and c 6. Draw the ring-flip isomer for the following substituted cycloalkane. Circle the most stable conformation.       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