Effect of intramolecular hydrogen bonding on the relative acidities of substituted salicylic acids in benzene solution

The relative acidities of fifteen 4- and 5-substituted salicylic acids were determined in benzene solution by potentiometric titration. The potentials at half neutralization (h.n.p.) relative to that of salicylic acid were considered to measure the acidities of the substituted acids relative to the parent acid. These potentials, designated by Δ hnp , gave a significantly better correlation with Hammett's sigma constants in an equation of the form proposed by Jaffe, Δ hnp = ρ 1 σ 1 + ρ 2 σ 2 , than in a simple Hammett equation, Δ hnp = ρ 1 σ 1 . In these equations the subscripts 1 and 2 refer to the position of a substituent relative to the carboxyl group and to the phenolic group respectively. The value of ρ 2 /ρ 1 was found to be 0.4, indicating that the electronic effect of a substituent on the acid strength via the phenolic hydrogen-bonded path is almost half as large as the direct effect through the carboxyl group. These results, together with the fact that in aqueous solution there is very little if any transmission via the phenolic group, are discussed in terms of intramolecular hydrogen bonding of salicylic acids in benzene and in water.