A Study of Solvent Effects in the Solvolysis of Propargyl Chloroformate.

Malcolm J D'Souza, Anthony M Darrington, Dennis N Kevill
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Abstract

The specific rates of solvolysis of propargyl chloroformate (1) are analyzed in 22 solvents of widely varying nucleophilicity and ionizing power values at 25.0 °C using the extended Grunwald-Winstein equation. Sensitivities to solvent nucleophilicity (l) of 1.37 and to solvent ionizing power (m) of 0.47 suggest a bimolecular process with the formation of a tetrahedral intermediate. A plot of the rates of solvolysis of 1 against those previously reported for phenyl chloroformate (2) results in a correlation coefficient (R) of 0.996, a slope of 0.86, and an F-test value of 2161. The unequivocal correlation between these two substrates attest that the stepwise association-dissociation (A(N) + D(N)) mechanism previously proposed for 2 is also operative in 1.

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氯甲酸丙炔溶剂分解的溶剂效应研究。
利用扩展的Grunwald-Winstein方程,在25.0°C下,分析了氯甲酸丙炔酯(1)在22种亲核性和电离功率值变化很大的溶剂中的溶剂溶解比速率。对溶剂亲核性(l)的敏感性为1.37,对溶剂电离力(m)的敏感性为0.47,表明这是一个形成四面体中间体的双分子过程。将1的溶剂溶解速率与先前报道的氯甲酸苯酯(2)的溶剂溶解速率进行对比,得出相关系数(R)为0.996,斜率为0.86,f检验值为2161。这两种底物之间的明确相关性证明,先前为2提出的逐步结合-解离(A(N) + D(N))机制也适用于1。
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