## Abstract The gasβphase thermal decomposition of 5βethylβ1βpyrroline has been studied in the temperature range 721β786 K. The decomposition appears to proceed by two pathways, one a radical route yielding pyrrole, ethylene and ethane as major products, and the other a molecular hydrogen eliminati
The Gas-phase thermal unimolecular isomerization of n-propylidenecyclopropylamine to 5-ethyl-1-pyrroline
β Scribed by Alan T. Cocks; Kurt W. Egger
- Publisher
- John Wiley and Sons
- Year
- 1972
- Tongue
- English
- Weight
- 279 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0538-8066
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β¦ Synopsis
The gas-phase thermal isomerization of N-propylidenecyclopropylamine has been studied in the temperature range of 573" to 635Β°K. The reaction is homogeneous and kinetically first order and yields 5-ethyl-1-pyrroline as the sole product. The rate constants are independent of pressure in the range of 2.5 to 55 torr and fit the Arrhenius relationship log k(sec-') = (14.05 f 0.06) -(47.77 0.16)/0 where 6 = 2.303 RT in units ofkcal/mole, or log k(sec-l) = (14.05 k 0.06) -(199.9 0.7)/8, where e = 2.303RT in kJ/mole. From considerations of a biradical pathway it is concluded that the resonance stabilization energy of the substituted 2-aza-ally1 radical is very similar to that of the methallyl radical.
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