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The acid-catalysed hydrolyses of some N-(para-substituted phenyl)propane-1,3-sultams have been studied in aqueous acidic solutions. The rate maxima observed are shown to be consistent with an A-2 mechanism in which extensive protonation of the substrate occurs. Values of pKBH+ for the sultams have been determined.
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Bekdemi̇r et al. (1993) studied this question.
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