## Abstract In the present paper, kinetic isotope effects of the title reaction are studied with canonical variational transition state theory on the modified Wang Bowman (MWB) potential energy surface (PES) (__Chem Phys Lett__ 2005, 409, 249) and the ab initio calculations at the quadratic configu
Kinetic isotope effects in the reaction H + C2H4 → C2H5
✍ Scribed by Ko-Ichi Sugawara; Kiyoshi Okazaki; Shin Sato
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- English
- Weight
- 416 KB
- Volume
- 78
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
The high-pressure bmiting rate constants of the reactlons between H or D atoms and three isotopic ethylenes have been measured in the temperature range 206-461 K. PractxaUy no isotope effects due to the differences between the ethylefies could be observed This result does not agree with the prediction recently made by the activated complex theory.
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The initial rates of formation of the major products in the thermal reactions of ethylene at temperatures in the neighborhood of 800 K have been measured in the presence and absence of the additives neopentane and ethane. It has been shown that in the absence of the additive the main initiation proc
Formation of methyl radicals via the consecutive reactions H+C2H,+M+C2H,+M ( I ) and H+CLH,+CH,+CH3 (?a) was initiated by pulse radiolysis of IO-100 mbar Hz in the presence of ethylene. The kinetics of CH, were studied by monitoring the transient infrared absorption at the Q( 3, 3) line of the u,=O+