Abstract

The variation with concentration of the viscosity and density of aqueous solutions of anilinium chloride, and of some C- and N-methyl substituted anilinium chlorides, has been measured in the presence of sufficient hydrochloric acid to suppress hydrolysis. A suitable method of evaluating viscosity B coefficients for these organic cations from these data has been developed. It has been shown that the ratio of the B coefficient for the organic cation (B+) to its limiting apparent molar volume (Φ+°) increased slightly with increasing methyl substitution in the ring. For the N-methylated cations, on the other hand, B+/Φ+° fell rapidly as the number of substituent groups increased. This behaviour can be understood by assuming that increasing N-methyl substitution makes it progressively more difficult for a primary hydration shell to form around the charged nitrogen atom, and that insertion of methyl groups in the aromatic ring has little effect on this hydration process.

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