AbstractEugen Bomberger's original work was concerned with the rearrangement of the substituted N-phenylhydroxylamines, but the mechanism responsible for the wide variety of products has remained unsettled.First, this investigation was concerned with a suitable synthesis for the substituted N-alkyl-N-phenylhydroxylamines. Secondly, a better understanding of the mechanism could be accomplished by the identification of the decomposition products and through a kinetic study of the rearrangement utilizing ultraviolet spectroscopy. The study was successful with the product identification of five decomposed substituted N-.phenylhydroxylamines, but numerous products, which interfered with the kinetic study, were isolated from the rearrangement and only uninterpretable kinetic data could be collected.Ball State UniversityMuncie, IN 47306
| Identifer | oai:union.ndltd.org:BSU/oai:cardinalscholar.bsu.edu:handle/180201 |
| Date | 03 June 2011 |
| Creators | Hartzell, Stephen L. |
| Contributors | Kruger, Terry L. |
| Source Sets | Ball State University |
| Detected Language | English |
| Format | v, 54 leaves : ill. ; 28 cm. |
| Source | Virtual Press |
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