Abstract
A range of exchange-labile and non-labile metal-hydroxide species readily promote the hydrolyses of 2,4-dinitrophenyl acetate and 4-nitrophenyl acetate. Kinetic studies (25ºC, I 1.0 mol dm-3 NaClO4) show that these processes follow shallow Bronsted slopes (β 0.33 and 0.40 respectively) which extend over a range of 1010 in nucelophile basicity. A correlation is reported which allows the prediction of reaction rates between [CO(NH3)5OH]2+ and other activated charge-neutral carbonyl compounds.

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