We wish to report the polarographic study of two series of disubstituted diimides in 70% AQUEOUS ETHANOL WITH O.&N potassium chloride as supporting electrolyte at 30.0°C(\*). See Table I.
✦ LIBER ✦
The kinetics and linear free energy correlation of the alcoholyses of some N-aroyl-N′-phenyl diimides and N-benzoyl-N′-aryl diimides
✍ Scribed by Theophile Carty; Jesse M. Nicholson
- Book ID
- 104249368
- Publisher
- Elsevier Science
- Year
- 1970
- Tongue
- French
- Weight
- 141 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
A few years ago, we reported that the alcoholysis of N-BenoyI-N'-phenyldiimide led to the (21 formation of phenyl radicals.
Thus this reaction sequence was indeed unique, since it was a heterolysis, which was followed by a homolysis in a polar media.
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