## Abstract The kinetics of the gas‐phase decomposition of 1,2‐epoxycyclohexane has been studied over the temperature range 680–740 K at pressures between 1.6 and 6 torr. Isomerization to cyclohexanone and 2‐cyclohexen‐1‐ol accounts for ca. 97% of the primary reaction products and occurs by first‐o
Gas-phase thermal isomerization of hexachlorocyclopropane
✍ Scribed by Juan José Cosa; Mauricio Hamity
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 382 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
The gas-phase thermal isomerization of hexachlorocyclopropane to hexachloropropene at 208-283OC is first order and unaffected by changes in the surface-to-volume ratio or by the addition of iodine, tetrachloroethylene, and oxygen. The first-order rate constants fit the Arrhenius equation log k(s-') = (15.74 f 0.22) -(45,660 f 526)/4.576T
The reaction was interpreted as an unimolecular process taking place with chlorine atom migration. A comparison of the reactivities of several chlorocyclopropanes is made.
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The gas phase thermal isomerization of 4-acetyl-5-methyl-isoxazole affords 3-cyano-2,4-pentanedione as the only product in good agreement with previous proposed isomerization mechanism for isoxazoles. On the other hand, kinetic parameters and MO theoretical calculations do not agree with those previ
## Abstract The kinetics of the gas‐phase decomposition of bicyclo[4.1.0]heptane has been studied over the temperature range of 708–769 K at pressures between 1 and 17 torr. Isomerization to 1‐methylcyclohex‐1‐ene, methylenecyclohexane, and cycloheptene accounts for 96–98% of the primary reaction p
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## Abstract \documentclass{article}\pagestyle{empty}\begin{document}$ \left[{{\rm C}\_{{\rm 10}} {\rm H}\_{{\rm 14}} } \right]\_{}^{\_.^ + } $\end{document} ions have been generated from a number of adamantanoid compounds, both by ionization and ionization followed‐by fragmentation. Metastable ion