Affiliation:
1. Venable and Kenan Chemical Laboratories, The University of North Carolina Chapel Hill, North Carolina 27514
Abstract
Abstract
Simplified quasi-equilibrium calculations performed on the mass spectra of dihalosubstituted phenyl acetates and acetanilides again uncover the same substituent effects on the rise of K with E for the loss of ketene from phenyl acetates as was determined for the monosubstituted phenyl acetates. However, a new effect is found for the disubstituted acetanilides, removal of excitation probability for low-lying energy states of the molecular ion. This effect parallels the removal of transition probability for the lowest excited state of the neutral molecule.
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy,Mathematical Physics
Cited by
6 articles.
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