Master's Theses

Document Type

Thesis - campus only access

Date of Award

Fall 1974

Degree Name

Master of Science (MS)

Department

Chemistry

Advisor

James H. MeMechan

Abstract

The use of nuclear magnetic resonance (NMR) has expanded continuously in the last few years as an analytical tool. It has recently been stated that structures of 45 to 55% of all aromatic compounds can be completely determined from their proton NMR structure. The remaining aromatic compounds can be analyzed sufficiently to estimate structure with considerable accuracy. The estimation is accomplished by integration for total numbers of protons, chemical shift measurement for proton types, and characteristic splitting pattern evaluation for finding neighboring protons.

Comments

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Rights

© 1974 Ronald W. Wise

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