Reatividade Relativa em Solvólise Nucleofílica de Cloretos de Arilsulfenila, Arilcarbonila, Arilsulfonila, Arilmetila e de Arila


Autoria(s): Hirata,Rodobiko; Kiyan,Nilo Zengo; Miller,Joseph
Data(s)

01/06/1997

Resumo

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.

Formato

text/html

Identificador

http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40421997000300003

Idioma(s)

pt

Publicador

Sociedade Brasileira de Química

Fonte

Química Nova v.20 n.3 1997

Palavras-Chave #2-propanolysis #electrophilic carbon and sulphur centres #solvolysis mechanism
Tipo

journal article