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Mass spectrometric investigation of bimolecular compounds

✍ Scribed by George W. Heunisch; Gary W. Keen


Publisher
John Wiley and Sons
Year
1971
Tongue
English
Weight
500 KB
Volume
5
Category
Article
ISSN
1076-5174

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✦ Synopsis


Two points involving molecular structure have been investigated using mass spectrometry. First, mass spectra have been obtained that indicate a rapid means for differentiating bimolecular compounds from other structural isomers. Second, the mass spectrometric method has been used to evaluate bonding within bimolecular compounds. Quinone compounds have been reacted with dihydroxybenzene compounds to produce quinhydrone products, and upon mass spectrometric analysis, the quinhydrones decompose to regenerate derivatives of the starting materials. Evaluation of the decomposition products suggests that the hydroxyl hydrogens are involved in a resonance structure, and while in symmetrical quinhydrones, the hydroxyl hydrogens are probably associated equally with each reactant, unsymmetrical quinhydrones generate an unbalanced electronic distribution that eliminates the complete equivalency of the hydrogens.


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## Abstract Under electron impact conditions the mass spectrometric behaviour of secondary and tertiary __para__‐substituted benzenesulphinamide derivatives has been studied. The fragmentation modes of these compounds, including a characteristic H~2~O loss from the molecular ions of __N__‐benzylami