The Photolysis of T-Butyl Nitrite in Hydrocarbon Solution.

Abstract

The photolysis of t-butyl nitrite in hydrocarbon solvents having abstractable hydrogen atoms results in the formation of t-butanol and solvent-derived nitroso dimer and/or oxime. The quantum yield is higher in cyclohexene than in cyclohexane or cyclopentane. There are many side reactions, two of which are photochemical decomposition of nitroso dimer and the Bamberger reaction. (Author)

Document Details

Document Type
Technical Report
Publication Date
Aug 01, 1973
Accession Number
AD0768782

Entities

People

  • Alan C. Duckworth
  • Lester P. Kuhn

Organizations

  • Ballistic Research Laboratory

Tags

DTIC Thesaurus Topics

  • Acyclic Hydrocarbons
  • Alkanes
  • Chemical Compounds
  • Chemical Reactions
  • Cyclic Compounds
  • Cyclic Hydrocarbons
  • Cyclohexanes
  • Cyclohexenes
  • Cyclopentanes
  • Decomposition
  • Dissociation
  • Hydrocarbons
  • Hydrogen
  • Photolysis
  • Quantum Yields
  • Side Reactions

Fields of Study

  • Chemistry

Readers

  • Organic Chemistry
  • Wave Propagation and Nonlinear Chaotic Dynamics.

Technology Areas

  • Quantum Computing