Protonation constants of a number of mono- and disubstituted pyridines
were determined potentiometrically in 0, 10, 20, 30, 40, 50, 60, 70,
80% (v/v) ethanol-water mixtures at 25 degrees C with an ionic strengt
h of 0.1 M. Data were calculated by a computer programme. The logarith
m of the protonation constants of pyridines linearly decreased with in
crease of ethanol contents but the values determined in water and 80%
ethanol did not follow this linear trend. Furthermore, the effects of
the substituents on the basicity of pyridine, the additivities of thes
e effects and the applicability of the Hammett equation to the behavio
ur of substituents are discussed.