Department
Chemistry
Degree Name
Master of Science (MS)
Abstract
This study is a survey of the effects on the chemical shift of the olefinic protons of cinnamic acids and some other styrenes when various substituents are present. Cinnamic acids were chosen as the model compounds because they are easily synthesized, handled, and purified. Compared to many of the other olefinic compounds, they give simple and uncomplicated spectra. They also provide applications of many of the basic principles that regulate the chemical shift. All of the types of shielding are found in these compounds, caused either by the ring or the substituents on the ring. Effects of stereochemistry can be seen on the ortho-substituted compounds, such as in the cis-cinnamic acids.
Keywords
Alkenes, Stereochemistry, Molecular rotation, Electromagnetic fields, Cinnamic acid, Magnetic shielding
Advisor
Dr. James H. McMechan
Date of Award
Fall 1972
Document Type
Thesis - campus only access
Recommended Citation
Holstein, Alfred H., "The Nuclear Magnetic Resonance Spectra of Styrenes and Related Compounds" (1972). Master's Theses. 1352.
DOI: 10.58809/ZCSU1865
Available at:
https://scholars.fhsu.edu/theses/1352
Rights
© The Author(s)
Comments
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