Kinetic studies on the effect of acidity and temperature on the loss of optical activity of some butanediols

1984 ◽  
Vol 37 (4) ◽  
pp. 767 ◽  
Author(s):  
KP Herlihy

In aqueous perchloric acid, butane-1,2-diol (1) and butane-2,3-diol (2) give carbonyls and butane-1,3-diol (3) gives alkenols. The rate of loss of optical activity has been determined for these diols and butan-2-ol (4) over a range of temperatures and acidities. In 1 M acid at 100�C, the rates for (1), (2), (3) and (4) are in the ratio of 1 : 2.3 : 3.7 : 45 respectively. The activation parameters are similar for all the alcohols. Hammett acidity plots give slopes of c. 0.8 for the diols and of 1 for butan-2-ol. These variations in these kinetic parameters are discussed in terms of whether hydroxyl group substitution in butan-2-ol affects the mechanism of its reaction in these circumstances.

1972 ◽  
Vol 50 (19) ◽  
pp. 3129-3134 ◽  
Author(s):  
Donald G. Lee ◽  
Matthijs Van Den Engh

The kinetics of the oxidation of tetrahydrofuran by ruthenium tetroxide in aqueous perchloric acid solutions have been investigated. The rate of reaction is found to be directly dependent on the concentrations of oxidant and reductant, but inversely dependent on the acidity of the medium. A mechanism involving hydride abstraction in the rate determining step was found to be consistent with the evidence obtained from isotopic labeling and an analysis of the activation parameters (ΔH≠ = 14.0 kcal/mol, ΔS≠ = −18.4 e.u.) of the reaction. This conclusion is further substantiated by noting the similarity between the reactions of ruthenium tetroxide with alcohols and ethers.


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