The gas phase iodination of cyclobutane was studied spectrophotometrically in a The early stage of the reaction static system over the temperature range 589" to 662ยฐK. was found to correspond to the general mechanism where the Arrenius parameters describing kl are given by log kl/M-' sec-' = 1 1.
Kinetics of the gas-phase reaction of allyl alcohol with iodine. The heat of formation and stabilization energy of the hydroxyallyl radical
โ Scribed by Ze'ev B. Alfassi; David M. Golden
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- English
- Weight
- 430 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0538-8066
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โฆ Synopsis
Abstract
The reaction of iodine with allyl alcohol has been studied in a static system, following the absorption of visible light by iodine, in the temperature range 150โ190ยฐC and in the pressure range 10โ200 torr. The rateโdetermining step has been found to be
equation image
and k~3~ is consistent with the equation
equation image
From the activation energy and the assumption E~โ3~ = 1 ยฑ 1 kcal mol^โ1^, it has been calculated that
equation image
kcal mol^โ1^. The stabilization energy of the hydroxyallyl radical has been found to be 11.4 ยฑ 2.2 kcal mol^โ1^.
๐ SIMILAR VOLUMES
## Abstract The rate of the reaction of cyclopentadiene with iodine has been followed spectrophotometrically over the temperature range 171.7ยฐ to 276.5ยฐC. The reaction first proceeds almost to the point of equilibrium with cyclopentadienyl iodide and HI, although the final products are fulvalene an
The kinetics of the gas-phase thermal iodination of hydrogen sulfide by 12 to yield HSI and HI has been investigated in the temperature range 555-595 K. The reaction was found to proceed through an I atom and radical chain mechanism. Analysis of the kinetic data yields log k (l/mol-sec) = (11.1 f 0.
The gas-phase dehydrogenation of cyclopentene to cyclopentadiene catalyzed by iodine in. the range 178-283'C has been found to obey a rate law consistent with the slow rate-determining step, I + c-C5Hs --t HI + c-C5H, , log [ka/(l moleL1 sec-')I = 10.25 \* 0.08 -(12.26 f 0.18)/0, where 0 = 2.303RT i
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Absolute rate constants for the gas phase reaction of OH radicals with pyrrole tk,) and thiophene ( k , ) have been measured over the temperature ranges 298-440 and 274-382 K, respectively, using the flash photolysis-resonance fluorescence technique. The rate constants obtained were independent of t