FREE RADICALS BY MASS SPECTROMETRY. XXXII. THERMAL DECOMPOSITION OF CYCLOPENTYL RADICALS,

Abstract

At low pressures and elevated temperatures cyclopentyl radicals are found to dissociate mainly by two modes of reaction: about 34% by loss of H atom to form cyclopentene, and about 66% by a C-C bond rupture to form ethylene and allyl radicals. Under the conditions employed no evidence for a third possible mode, the loss of H2 to form cyclopentenyl radical, could be found. It is estimated that an incidence of 2% of the latter could have been detected. (Author)

Document Details

Document Type
Technical Report
Publication Date
Jul 15, 1964
Accession Number
AD0614505

Entities

People

  • F. P. Lossing
  • T. F. Palmer

Organizations

  • National Research Council Canada

Tags

DTIC Thesaurus Topics

  • Acyclic Hydrocarbons
  • Alkenes
  • Chemical Compounds
  • Chemical Synthesis
  • Chemistry
  • Cyclic Hydrocarbons
  • Cyclopentenes
  • Decomposition
  • Ethylenes
  • Free Radicals
  • Hydrocarbons
  • Mass Spectrometry
  • Organic Chemistry
  • Spectrometry

Fields of Study

  • Chemistry

Readers

  • Organic Chemistry
  • Thermal Physics or Thermal Science.