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β-deuterium kinetic isotope effects in the solvolysis of 2-aryl-1,1,1-trifluoro-2-propyl tosylates and of 2-aryl-2-profyl p-nitrobenzoates. Evidence for a variation of the contribution of α-methyl substituent in stabilizing cationic reaction centers with different electron demand

✍ Scribed by Kwang-Ting Liu; Yuh Wern Wu


Publisher
Elsevier Science
Year
1986
Tongue
French
Weight
251 KB
Volume
27
Category
Article
ISSN
0040-4039

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✦ Synopsis


A very high S-deuterium kinetic isotope effect, k(CH3)/k(CD3) =2.l3 at ~o'c, was found for the solvolysis of 2-(3'-chlorophenyl)-l,l,l-trifluoro-2propyl tosylate(&) and the a-CD3 analogue