Deuterium isotope effects in the solvolysis of benzal chlorides. 4. Salt effects and .alpha.-deuterium isotope effects

1981 ◽  
Vol 103 (4) ◽  
pp. 880-883 ◽  
Author(s):  
V. P. Vitullo ◽  
F. P. Wilgis
1979 ◽  
Vol 44 (1) ◽  
pp. 110-122 ◽  
Author(s):  
Jiří Velek ◽  
Bohumír Koutek ◽  
Milan Souček

Competitive hydration and isomerisation of the quinone methide I at 25 °C in an aqueous medium in the region of pH 2.4-13.0 was studied spectrophotometrically. The only reaction products in the studied range of pH are 4-hydroxybenzyl alcohol (II) and 4-hydroxystyrene (III). The form of the overall rate equation corresponds to a general acid-base catalysis. The mechanism of both reactions for three markedly separated pH regions is discussed on the basis of kinetic data and solvent deuterium effect.


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