Abstract
Studies of the nucleophilic addition of tertiary amines to acrylamide monomers in water in the presence of hydrogen chloride at initial and deeper conversions revealed the presence of special concentration effects, which strongly depended on the structure of the reagents. Viscosity isotherms were studied to show that the reagents in the systems studied experienced active association. The kinetic patterns obtained were explained by changes in the composition and structure of the associates.
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