ISSN 1017-2548(Print)
ISSN 2234-8530(Online)
Volume 29, Number 5
JKCSEZ 29(5)
October 20, 1985 

Nucleophilic substitution reactions between Alkanesulfonylchlorides and p-substituted anilines in methanol-acetonitrile mixture have been studied kinetically. Reactivities of substrates, substituent effects of nucleophile and solvent effects indicate that the studied reaction proceeds via SN2. The kinetic results show that transition state of the reaction between i-PSC and anilines becomes looser as the composition of methanol increases.