首页> 外文期刊>Russian Journal of General Chemistry >Kinetics and Mechanism of Monomolecular Heterolysis of Commecial Organohalogen Compounds: XXI. Solvent Efect on the Rate of 1-Methyl-1-chlorocyclopentane Heterolysis. Correlation Analysis of Solvation Effects
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Kinetics and Mechanism of Monomolecular Heterolysis of Commecial Organohalogen Compounds: XXI. Solvent Efect on the Rate of 1-Methyl-1-chlorocyclopentane Heterolysis. Correlation Analysis of Solvation Effects

机译:商业有机卤素化合物的单分子杂解动力学和机理:XXI。溶剂对1-甲基-1-氯环戊烷杂解速率的影响。溶剂化效应的相关性分析

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摘要

Hetreolysis of 1-methyl-1-chlorocyclopentane in protic and aprotic solvents occurs by the E1 mechanism. The reaction rate in aprotic solvents or in a set of protic and aprotic solvents in satisfactorily described by the parameters of the polarity and electrophilicity or ionizing power of the solvents. In protic solvents, the reaction rate grows with increasing polarity or ionizing power of the solvent and decreases with increasing nucleophilicity.
机译:1-甲基-1-氯环戊烷在质子传递和非质子传递溶剂中的水解都通过E1机理进行。通过溶剂的极性和亲电性或电离能力的参数令人满意地描述了在质子惰性溶剂或一组质子和非质子溶剂中的反应速率。在质子溶剂中,反应速率随着溶剂极性或电离能力的增加而增加,而随着亲核性的增加而降低。

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