The alkaline hydrolysis of a polyacrylonitrile suspension was carried out i
n a water/ethanol mixture at 75 degrees C. The product structure was studie
d by means of solid state C-13 NMR spectroscopy. The hydrolyzed samples con
tain up to 20% of amidines, which are formed in the nearest neighborhood of
the COONa groups. Amidines are relatively stable under the given reaction
conditions up to almost complete conversion of the nitrile groups, then bei
ng hydrolyzed gradually into amides. After complete hydrolysis of the amidi
nes, the resulting poly[(acryl amide)-co-(sodium acrylate)] exhibits a Bern
oulli triad distribution of the comonomer units. The data obtained might be
useful in elucidating the reaction mechanism.