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Issue 7, 1970
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Common intermediates in the electron impact decomposition of substituted nitrobenzenes and anisoles

Abstract

The shapes of “metastable peaks” are used to establish that M+– NO ions from substituted nitrobenzenes and M+– CH3 ions from substituted anisoles decompose further via common intermediates, and that in this further decomposition m- and p-substituents are not randomised relative to the reaction centre.

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Article information


J. Chem. Soc. D, 1970, 412-413
Article type
Paper

Common intermediates in the electron impact decomposition of substituted nitrobenzenes and anisoles

B. Davis and D. H. Williams, J. Chem. Soc. D, 1970, 412
DOI: 10.1039/C29700000412

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