𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Kinetic Study of the 2-Naphthyl (C 10 H 7 ) Radical Reaction with C 2 H 2

✍ Scribed by Park, J.; Nguyen, Hue M. T.; Xu, Z. F.; Lin, M. C.


Book ID
121328935
Publisher
American Chemical Society
Year
2009
Tongue
English
Weight
554 KB
Volume
113
Category
Article
ISSN
1089-5639

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Temperature-dependent kinetics studies o
✍ JΓΌrg Eberhard; Carleton J. Howard πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 571 KB

The rate coefficients for the gas-phase reactions of C,H,O;, and n-C3H,0, radicals with NO have been measured over the temperature range of (201 -403) K using chemical ionization mass spectrometric detection of the peroxy radical. The alkyl peroxy radicals were generated by reacting alkyl radicals w

Kinetics of the reaction: 2C2H4 β†’ C2H5 +
✍ G. Ayranci; M. H. Back πŸ“‚ Article πŸ“… 1983 πŸ› John Wiley and Sons 🌐 English βš– 929 KB

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

Kinetic study of the gas-phase reaction
✍ Shozo Furuyama; David M. Golden; Sidney W. Benson πŸ“‚ Article πŸ“… 1970 πŸ› John Wiley and Sons 🌐 English βš– 389 KB

The kinetics of the gas-phase dehydrogenation of cyclopentane to cyclopentene is found to be consistent with a slow attack by a n I atom (step 4, text) on cyclopentane in the range 282-382OC. The measured rate constants fit the Xrrhenius equation, log k, = 11.95 f 0.08 -(24.9 f 0.23)/0 1 mole-l sec-

Theoretical studies of the radical react
✍ Shogo Sakai; Mark S. Gordon πŸ“‚ Article πŸ“… 1986 πŸ› Elsevier Science 🌐 English βš– 351 KB

Ab initio molecular orbltal calculations on the transitton states and barrter heights for the addition of atomtc hydrogen to sllaethylene are carried out. The activation energy for the addition to the silicon site is lower than that to the carbon site, wlnle the exothermicity 1s smaller.