Abstract
The proton magnetic resonance chemical
shifts of N-methyl protons in para-substituted
NN-dimethylanilines have been correlated with the
Hammett �- value of the para
substituent. The correlation yields �- values of 1.57 � 0.09 and 0.85 � 0.09
for the para nitroso and para 4'-dimethylaminobenzoyl
substituents, respectively. The solvent shift of the N-methyl protons between
chloroform and benzene solutions also fits a linear correlation with Hammett �-,
and yields �- = 1.52 � 0.11 for the para-nitroso
substituent.
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