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The fragmentation of 1-phenyl-2-propen-1-ol under electron impact

✍ Scribed by Jean-Pierre Denhez; Madeleine Corval; Pierre Dizabo

Publisher
John Wiley and Sons
Year
1981
Tongue
English
Weight
409 KB
Volume
16
Category
Article
ISSN
1076-5174

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✦ Synopsis

Abstract

The electron impact mass spectra of 1‐phenyl‐2‐propen‐1‐ol and its specifically deuterated analogues have been investigated. Most of the decomposition pathways involve skeletal rearrangements or hydrogen atom transfers, such that a rearrangement of the excited molecular ions of 1‐phenyl‐2‐propen‐1‐ol to molecular ions of cinnamic alcohol and/or cinnamaldehyde can be anticipated.

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