Phenol pyrolysis has been studied in a turbulent flow reactor by analyzing concentration-time profiles of three major decomposition products: carbon monoxide, cyclopentadiene, and benzene. Experimental conditions were P = 1 atm, T = 1064 -1162 K, and initial phenol concentrations of 500-2016 ppm. Th
Gas-phase pyrolysis of neopentyl bromide
✍ Scribed by Robert L. Failes; Yousuf M. A. Mollah; Jacob S. Shapiro
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 537 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
Abstract
The pyrolysis of gaseous neopentyl bromide to 2‐methyl‐2‐butene, 2‐methyl‐1‐butene, and hydrogen bromide was studied under conditions of maximal inhibition by cyclohexene over the temperature range of 389−444°C. This reaction was shown to beconsistent with a first‐order homogeneous molecular process, with Arrhenius parameters of E = 247 ± 5 kJ/mol and log A (sec^−1^) = 14.2 ± 0.3. Examination of the uninhibited reaction showed it to be a radical process, simpler than that with neopentyl chloride, there being only one propagation step, thedissociation of the γ‐radical to 1,1‐dimethylcyclopropane and a bromine atom.
📜 SIMILAR VOLUMES
## Abstract Experimental evidence is presented for a unimolecular gas‐phase Wagner‐Meerwein shift in neopentyl chloride pyrolysis. In the decomposition of α,α‐neopentyl chloride‐__d__~2~ at 445°C, maximally inhibited by cyclohexene, the initial products were isotopically pure 2‐methyl‐1‐butene‐__d_