1,2-Dimethylcyclohexane

The preferred chair has both methyls equatorial, which minimises 1,3-diaxial repulsions. In the 1,2-disubstituted case this is possible only for the trans-isomer, which is 6 kJ/mol more stable than the cis-isomer (in the 1,2-cis isomer one of the methyl groups must be axial).

The <em>cis</em>- and <em>trans</em>-isomers of 1,2-dimethylcyclohexane
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