首页> 外文期刊>Química Nova >Reatividade Relativa em Solvólise Nucleofílica de Cloretos de Arilsulfenila, Arilcarbonila, Arilsulfonila, Arilmetila e de Arila
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Reatividade Relativa em Solvólise Nucleofílica de Cloretos de Arilsulfenila, Arilcarbonila, Arilsulfonila, Arilmetila e de Arila

机译:芳硫基,芳基羰基,芳基磺酰基,芳基甲基和芳基氯化物的亲核溶剂解中的相对反应性

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摘要

The experimental results for the 2-propanolysis of benzoyl, benzyl, benzene sulphenyl and benzene sulphonyl chlorides obtained by conductimetric technique were compared with estimates for chlorobenzene which is extremely unreactive as an electrophile. We thus obtained the following reactivity sequence: PhSCl>PhCOCl>PhSO2Cl>PhCH2 Cl>PhCl with rate-coefficiente ratios (in the same order): 9.5 x 10(4) : 1: 7.14 x 10-2 : 4.7 x 10-3 : about 10-26. We have discussed these results in specific terms and with the aid of general conclusions which stem from our own classification of electrophiles.
机译:将通过电导技术获得的苯甲酰基,苄基,苯磺酰基和苯磺酰氯的2-丙分解实验结果与对作为亲电试剂极不反应的氯苯的估计值进行了比较。因此,我们获得了以下反应序列:PhSCl> PhCOCl> PhSO2Cl> PhCH2 Cl> PhCl,速率系数比(相同顺序):9.5 x 10(4):1:7.14 x 10-2:4.7 x 10-3 :大约10-26。我们以特定的术语讨论了这些结果,并借助于归因于我们自己的亲电试剂分类的一般结论。

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