Abstract
AbstractThe u.v. and i.r. spectra of some arylidene derivatives of salicylic hydrazide have been studied. The u.v. spectra in organic solvents are considered in terms of medium effect and molecular structure. The changes of the spectra in buffer solutions are explained on the basis of the shifts in the acid‐base equilibrium set; the various pK values are determined and commented upon in relation to substituent effects. The main bands in the i.r. spectra are assigned and the shift in their positions is discussed in the light of substituent effects.
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