Abstract
The dipole moments of methyl, ethyl, n-propyl, n-butyl, amyl, and phenyl chloroformate as well as n-butyl formate in dilute benzene solution at 25 °C were determined. The experimental results suggest that the configuration of the chloro-esters differs from the configuration of the unchloroinated esters, viz. the ester hydrocarbon group and the chlorine atom are cis to each other.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
28 articles.
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