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Conformational effects in electron impact induced elimination reactions in the 1,2-diphenylethanol system.

โœ Scribed by M.E. Munk; C.L. Kulkarni; C.L. Lee; P. Brown

Book ID
104248833
Publisher
Elsevier Science
Year
1970
Tongue
French
Weight
253 KB
Volume
11
Category
Article
ISSN
0040-4039

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โœฆ Synopsis

The Tied effects of stereochemistry on the mass spectral fragmentation patterns of various isomeric sets of organic compounds have been reviewed critically recently (l), and it is obvious that most previous literature reports refer to epimers of cyclic compounds. Notable exceptions

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Stereochemistry and mechanism of electron impact induced elimination reactions in acenaphthenol and acetoxyacenaphthene
โœ Daryl D. Manhart; Peter Brown; Duncan H. Hunter ๐Ÿ“‚ Article ๐Ÿ“… 1977 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 659 KB

## Abstract The mechanisms for elimination of H~2~O from acenaphthenol and of AcOH from acetoxyacenaphthene under low energy conditions have been determined, using regiospecific and stereospecific deuterium labeling probes, and by measurement of ionization and appearance potentials for alternative