Carbon-14 and deuterium isotope effects in the borderline solvolysis of isopropyl .beta.-naphthalenesulfonate

1982 ◽  
Vol 104 (20) ◽  
pp. 5493-5494 ◽  
Author(s):  
Takashi Ando ◽  
Hiroshi Yamataka ◽  
Shinichi Tamura ◽  
Terukiyo Hanafusa

1978 ◽  
Vol 100 (8) ◽  
pp. 2570-2571 ◽  
Author(s):  
Clair J. Collins ◽  
Ben M. Benjamin ◽  
George W. Kabalka








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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