Abstract
The influence of activation methods and solid support on the reaction course of benzyl bromide, KCN, and toluene has been investigated. When KCN is not supported on alumina, the reaction under the mechanical agitation follows the aromatic electrophilic substitution pathway, while the reaction under sonication follows nucleophilic substitution. However, when KCN supported on alumina is employed, only the nucleophilic substitution product is obtained under both ultrasound and mechanical agitation.
Full Text
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call