Author:
Buncel E.,Strachan W. M. J.
Abstract
Study of the acid-catalyzed Wallach rearrangement of azoxybenzene is extended into the 100% H2SO4 region. The rate of formation of 4-hydroxyazobenzene can be followed spectrally in a straight-forward manner until close to 99% H2SO4, but in higher acidities sulfonation of this product becomes kinetically important. The advent of second equilibrium protonations of 4-hydroxyazobenzene and of 4-hydroxyazobenzene-4′-slfonic acid further complicate the azoxybenzene rearrangement as followed spectrally. Above 100% H2SO4 a second sulfonation is also observed. A method is given for dissecting the rate data for the primary rearrangement process from the first of the sulfonation reactions.The rate of the azoxybenzene rearrangement is observed to increase continuously up to 99.99% H2SO4 (the upper limit of the present kinetic method). This suggests that the second proton transfer step to azoxybenzene is rate-determining and not an equilibrium process. These results permit a clarification of a previously proposed mechanism (1).
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
29 articles.
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