N.M.R. Study of the Hydrogen Bonding Properties of 1,8-Cineole

Author: Swatek, Edwin Paul, III

Year: 1965

Degree: Bachelor's thesis

Advisor: Unknown, Unknown

Committee Member: Unknown, Unknown

Option: Chemistry

DOI: 10.7907/0krj-8084

Abstract

A study of the concentration dependence of the proton resonance signal of chloroform due to solvent-solute hydrogen bonding has indicated that 1,8-cineole is an appreciably stronger hydrogen bonding agent than is tetrahydrofuran, dioxane or diethyl ether. Comparisons were based on the magnitude of the difference between the positions of the chloroform resonance in the limits of dilute and concentrated solutions.

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