Abstract

This report details the study of the nucleophilic substitution of 1-benzyl-3,5-dibromo-lH-1,2,4-triazole. A variety of nucleophiles have been studied to date. The nucleophiles studied primarily fall into the categories of Phosphorous, Oxygen and Sul fur species. Some of the initially formed substitution products are thermally unstable and undergo unique rearrangements. The report describes the physical properties, 1H NMR, 13c NMR, IR and Mass spectra for all of the synthesized compounds. Possible mechanistic pathways are presented for the formation of the prepared compounds. Recommendations are made in order to suggest future research opportunities in this area.

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Graduation Date

1988

Semester

Summer

Advisor

Gupton, John T.

Degree

Master of Science (M.S.)

College

College of Arts and Sciences

Department

Chemistry

Format

PDF

Pages

88 p.

Language

English

Rights

Public Domain

Length of Campus-only Access

None

Access Status

Masters Thesis (Open Access)

Location

Orlando (Main) Campus

Identifier

DP0021932

Subjects

Arts and Sciences -- Dissertations, Academic; Dissertations, Academic -- Arts and Sciences

Accessibility Status

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Included in

Chemistry Commons

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