Author:
Abramovitch R. A.,Saha J. G.
Abstract
The decomposition of benzenediazonium borofluoride in a number of aromatic solvents has been studied. The main product is fluorobenzene but some substituted biphenyls are formed. The isomer ratios and apparent total rate ratios for these phenylations have been determined. The results are discussed and it is suggested that the reactive intermediate in the arylations is the phenyl diradical cation.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
38 articles.
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