کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5134628 | 1492953 | 2017 | 5 صفحه PDF | دانلود رایگان |

- Pyrolysis of exo-2-norbornyl formate is homogeneous, unimolecular, and first-order.
- Unusual products formation in pyrolysis of esters with the presence of a CβH bond.
- Experimentals suggests a concerted three-membered cyclic transition state mechanism.
The rate coefficient of the gas-phase pyrolysis or elimination of exo-2-norbornyl formate was determined in a deactivated, static reaction vessel over the temperature range 300-350 °C and pressure range 41-105 Torr. The substrate exo-2-norbornyl formate yielded surprisingly exo-2-norborneol and CO gas. This reaction, in the presence or absence of the free radical inhibitor toluene, proved to be homogeneous, unimolecular and follows a first-order rate law. The rate of equation is given by the following Arrhenius equation: log k1 (sâ1) = (13.85 ± 0.23) â (194.6 ± 2.7)kJ molâ1(2.303RT)â1, r = 0.9998.Experimental data suggested a semi-polar concerted three-membered cyclic transition state type of mechanism.
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Journal: Journal of Analytical and Applied Pyrolysis - Volume 124, March 2017, Pages 563-567