𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Thermal stability of cyclohexane and 1-hexene

✍ Scribed by Wing Tsang


Book ID
102929817
Publisher
John Wiley and Sons
Year
1978
Tongue
English
Weight
804 KB
Volume
10
Category
Article
ISSN
0538-8066

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

The mechanism and initial rates of decomposition of cyclohexane and 1‐hexene have been determined from single‐pulse shock‐tube experiments. The main initial processes involve isomerization of cyclohexane to 1‐hexene, followed by decomposition of 1‐hexene. From comparative rate experiments the following rate expressions have been derived:

The 1‐hexene bond‐braking reaction leads to an allylic resonance energy of 42.7 kJ and a heat of formation of allyl radicals of 176.6 kJ (300°K). There appear to be general relations relating the rate expressions for the decomposition of alkynes, alkanes, and alkenes. Studies on the induced decomposition of cyclohexane have also been carried out.


📜 SIMILAR VOLUMES


Kinetics of 1-hexene polymerization
✍ D. K. Dandge; J. P. Heller; C. Lien; K. V. Wilson 📂 Article 📅 1986 🏛 John Wiley and Sons 🌐 English ⚖ 464 KB 👁 2 views
Formation of H-atoms in the pyrolysis of
✍ Sebastian Peukert; Clemens Naumann; Marina Braun-Unkhoff; Uwe Riedel 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 647 KB

## Abstract Cyclohexane (cC~6~H~12~) plays an important role in the combustion of practical liquid fuels, as a major component of naphthenic compounds. Therefore, the pyrolysis of cyclohexane was investigated by measuring the formation of H‐atoms. The thermal decomposition of 1‐hexene (1‐C~6~H~12~)

Synthesis and thermal stability of some
✍ Ichiro Murata; Toshio Tatsuoka 📂 Article 📅 1975 🏛 Elsevier Science 🌐 French ⚖ 224 KB

We have recently developed a novel approach to the synthesis of thermally labile 1-benzothiepin (ljl) based on the rhodium complex promoted isomerisation of 4,5-benzo-3-thiatricyclo[4.1.0.02'71heptene (2).2) This achievement, as well as the ease of introducing suitable substituent into the bridgehea