Author Type

Graduate Student

Date of Award

1982

Document Type

Thesis

Publication Status

Version of Record

Submission Date

October 2026

Abstract

The kinetics of N,N-diethyl-p-phenylenediamine with monochloramine were investigated using spectrophotometric techniques. The oxidation proceeds by two sequential steps each involving one hydrogen atom. The starting material N,N-diethyl-p-phenylenediamine and the first oxidation product are both involved in acid-base equilibria which result in a complex dependence of the reaction rate on hydrogen ion concentration. The reactions were found to follow pseudo second order kinetics, first order with respect to each reactant, at a specific pH. In the presence of excess N,N-diethyl-p-phenylenediamine the formation of a dimer was observed. Mechanisms consistent with the experimental data are proposed.

Extent

87 p.

Comments

Thesis (M.S.)--Florida Atlantic University, 1982.|Thesis (M.S.)--Florida Atlantic University, 1982.

Identifier

FADT14146

Format

pdf

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