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Structural and stereochemical factors in the mass spectrometry of monocyclic hydrocarbons with geminal substituents

Journal Article · · Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States)
OSTI ID:7129391
This paper studies the mass spectra of geminally substituted monocyclic hydrocarbons of the composition C/sub 8/H/sub 16/-C/sub 11/H/sub 22/. An analogy in the principles of the decomposition of the molecular ions of geminally substituted cyclohexanes and cyclohexanes not having a geminal group in the molecule was established, as well as for the influence of stereochemical factors on the quantitative pattern of the mass spectra of the structural isomers. The comparative characteristics of the decomposition, under electron impact, of geminally substituted hydrocarbons of the cyclohexane and cyclopentane series were given. Diagnostic indexes for the identification of structural isomers were shown.
Research Organization:
Institute of Geology and Development of Combustible Minerals, Moscow
OSTI ID:
7129391
Journal Information:
Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States), Journal Name: Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States) Vol. 34:7,PT. 1; ISSN BACCA
Country of Publication:
United States
Language:
English