The PMR spectra of 2‐nitroacetanilide and often 4‐alkyl substituted derivatives have been measured. Two about equally stable conformers have been detected for the derivatives with the groups ‐CHPr i Bu t , ‐CHBu t 2 , and ‐C(OH)Bu t 2 . The conformational isomerism is caused by a hindered rotation about the bond between the alkyl groups and the benzene ring; rotational barriers have been determined of approximately 12, 22, and 21 kcal/mole, respectively. The preferred conformations and the rotational barriers are discussed for the alkyl groups ‐CH 2 Bu t , ‐CHMeBu t , and ‐CHPr i 2 .
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J. M. A. Baas (1972) studied this question.
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