Nanosecond laser flash photolysis studies have been carried out of the kinetics of inter- and intramolecular phenolic hydrogen abstraction by alkoxyacetophenone, 5-alkoxyindanone, and 4-alkoxybenzophenone triplets in acetonitrile and benzene solution. Information on the geometric requirements for abstraction by carbonyl n,π* and π,π* triplets is derived from the results for a series of ketones which contain a para-phenolic moiety attached via a para-oxyethyl linkage. For all of these compounds, the deuterium kinetic isotope effect on the triplet lifetime in acetonitrile solution indicates that triplet decay is determined by the rate of intramolecular abstraction of the remote phenolic hydrogen, which yields the corresponding phenoxyl−hemipinacol biradical. The biradicals have also been detected, and are about an order of magnitude longer-lived than the triplet in each case. For three of the compounds, the rates of the intramolecular process follow the same trend as that observed in the rates of bimolecular quenching of the parent methoxy-substituted ketones by p-cresol. Deviation from this trend is observed for the alkoxyindanone derivative, where an in-plane approach of the phenolic hydrogen to the carbonyl n-orbital is not possible. The trends in the rate constants for bimolecular quenching of a series of substituted benzophenones by p-cresol indicate that for n,π* triplet abstractions, the quenching mechanism is different for electron donor-substituted and electron acceptor-substituted ketones. For π,π* triplets and donor-substituted (n,π* triplet) benzophenones, abstraction is proposed to occur by a mechanism involving the intermediacy of a hydrogen-bonded exciplex, which yields the corresponding radicals by sequential electron- and proton-transfer. The rate constant for quenching by this mechanism thus depends mainly on the basicity of the ketone triplet state and the oxidation potential of the phenol.