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The hydroxide-, chymotrypsin-, and blood-catalyzed hydrolysis of a series of sodium 4-acyloxy-3-nitrobenzene sulfonates
The kinetics of the hydrolysis of a series of water-soluble aromatic esters (sodium 4-acyloxy-3-nitrobenzene sulfonates) were analyzed in order to determine the effect of a variety of substitutions (on the α-carbon of the acid group) upon the rate of reaction. The following was observed. That (a), t
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