Thesis (Ph. D.)--University of Wisconsin--Madison, 1950. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 170-173).

No description available.

Thesis (Ph. D.)--University of Wisconsin--Madison, 1937. / Typescript. Includes abstract and vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references.

Thesis (B.S.)--University of Missouri, School of Mines and Metallurgy, 1900. / The entire thesis text is included in file. Typescript. Illustrated by authors. Title from title screen of thesis/dissertation PDF file (viewed December 19, 2008)

This investigation was begun in order to determine the nature of the 104 degree melting compound prepared by Ashmore and to determine which isomers and their relative amounts are produced during bromination of phenylmercaptoacetic acid.

The photohydrodebromination of brominated paracyclophanes was studied to help elucidate the possible mechanistic pathways leading to product for bromoarenes in general. Several brominated [2.2]paracyclophanes were studied to determine the effect of substitution patterns on this reaction. [2.2]Paracyclophanes were chosen for this study in order to investigate possible intramolecular excimer formation as a route to product formation. The [2.2]paracyclophanes studied were 4-bromo-, pseudo-para-dibromo-, and pseudo-ortho-dibromo[2.2]paracyclophane. 5-Bromo[3.3]paracyclophane has also been studied to determine the effect of increased ring separation on the reaction. These brominated cyclophanes showed varying efficiencies of both intermolecular and intramolecular excimer formation. / Graduation date: 1993

Graduation date: 1992

No description available.

No description available.

Thesis (Ph. D.)--University of Chicago, 1938. / Lithoprinted. "Private edition, distributed by the University of Chicago libraries, Chicago, Illinois." Includes bibliographical references.