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i thought the most stable conformation of an isomer was always higher priotity equatorial and lower prioity axial..but i did a question where trans 3- methyl cyclohexanol (one equat the other axial) is less stable than cis 3- methyl cyclohexanol (equatorial for both)
..so what is actually the most stabe? with both positions eqatorial or one equatorial otherr axial?
thanks!
..so what is actually the most stabe? with both positions eqatorial or one equatorial otherr axial?
thanks!