Abstract
Data have been compiled for the pK values in certain
aqueous organic solvents at 25°C of about 70 meta-
or para-substituted benzoic acids, with a view to
proposing values of Hammett constants, σ, in the case of substituents
for which values cannot be based on the ionization of substituted benzoic
acids in water (Part I). The emphasis of the work is on the use of data for
the apparent pK values of the acids in 1 : 1
EtOH–H2O, i.e. a solvent made up of equal volumes
of ethanol and water. A calibration equation is derived relating substituent
effects measured in this solvent to those measured in water. On the basis of
this equation s values are proposed for 25 substituents, although some of the
values are subject to caveats, and several further substituents are also
discussed.
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