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On the reaction between ethylene and cyclopentene, a radical mechanism

✍ Scribed by Sidney W. Benson


Publisher
John Wiley and Sons
Year
1980
Tongue
English
Weight
258 KB
Volume
12
Category
Article
ISSN
0538-8066

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✦ Synopsis


Abstract

The bimolecular reaction
equation image
is shown to proceed via a simple, nonchain, radical mechanism:
equation image
with the net reaction the same as (1). Rate constants are estimated for each step and for each possible competing reaction and shown to yield minor or negligible side reactions in agreement with the observations of Lalonde and Back. Estimated and observed rate constants (1) and (1β€²) are in excellent agreement with the assumption that k'~‐1~ is a typical radical disproportionation with zero activation energy.

From the reported data a best value for kβ€²~1~ is
where ΞΈ = 2.303__RT__ kcal/mol.


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Theoretical study on the mechanism of th
✍ Xiu-Hui Lu; Li-Min Zhai; Ayi-Xnan Wang πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons 🌐 English βš– 323 KB πŸ‘ 2 views

## Abstract The mechanism of the cycloaddition reaction of singlet stannylene and ethylene or formaldehyde has been studied by using density functional theory. The geometrical parameters, harmonic vibrational frequencies and energies of stationary points for potential energy surface are calculated