"Benzyl chloride is a moderately reactive halide. Substitution of the Cl⁻ by other nucleophiles, e.g., HO⁻, AcO⁻, S₂O₃⁻, Br⁻ etc. proceeds almost quantitatively in solutions at convenient temperatures ... The object of this study was to investigate if the less basic t̲-butoxide in t̲-butyl alcohol would afford the same product, viz., stilbene; and, if so, by what mechanism. A study of the products and kinetics of the interaction between benzyl chloride and potassium t̲-butoxide in t̲-butyl alcohol therefore has been initiated"--Introduction, page 1.
Hanna, Samir B.
Antle, Charles E.
Wulfman, David S., 1934-2013
Chemical and Biochemical Engineering
M.S. in Chemical Engineering
University of Missouri at Rolla
v, 57 pages
© 1965 Der-Rong Chen, All rights reserved.
Thesis - Open Access
Library of Congress Subject Headings
Stilbene -- Analysis
Print OCLC #
Electronic OCLC #
Link to Catalog Recordhttp://laurel.lso.missouri.edu/record=b1068720~S5
Chen, Der-Rong, "The kinetics and mechanisms of the reaction of benzyl chloride with potassium t̲-butoxide in t̲-butyl alcohol" (1965). Masters Theses. 6957.