Abstract
We show a linear Hammett correlation in the conformational equilibrium of 2-aryloxycyclohexanones when the X substituent located para on the phenyl ring is electron withdrawing. This leads to the prediction of the equatorial position of the substituent in the 2-acyloxycyclohexanones. The conformational equilibria of 2-alcoxycyclohexanones (R = CH3 to C(CH3)3) also are examined.

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