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Reactions of o-halophenylazo phenyl sulfones and of (o-chlorophenyl)triphenylphosphonium iodide with sodium methoxide in methanol.

✍ Scribed by Bunnett, Joseph F.; Happer, Duncan A. R.


Book ID
124151471
Publisher
American Chemical Society
Year
1967
Tongue
English
Weight
538 KB
Volume
32
Category
Article
ISSN
0022-3263

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The kinetics of reaction of substituted O-benzoylbenzamidoximes with sodium methoxide in methanol were studied at 25 Β°C. The only reaction products are substituted benzamidoximes and methyl benzoates. The slope of the dependence of rate constant on sodium methoxide concentration gradually increases,