Elimination reactions of ions in the gas phase–I: Elimination of water and acetic acid in epimeric borneols and bornylacetates
✍ Scribed by R. Robbiani; J. Seibl
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- English
- Weight
- 557 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1076-5174
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Loss of water and acetic acid in the epimeric bornyl alcohols and acetates are shown to be analogous processes by specific ^2^H‐labelling. Among several competing mechanisms cis‐1,2‐elimination is the most important. Mctastable ion characteristics of this specific process exhibit some unusual features and its product is shown to have a different structure from that produced by the competing reactions.
📜 SIMILAR VOLUMES
DL-Mandelic acid was pyrolyzed in a static reaction vessel over the temperature range 300•1-340•0 °C and pressure range of the substrate 15•2-52•1 Torr. The reaction, in a seasoned vessel and in the presence of the free radical inhibitor cyclohexene, is homogeneous, unimolecular and obeys a first-or
## Abstract The gas‐phase pyrolysis of 2‐chloroethylbenzene and __p__‐methoxy‐2‐chloroethylbenzene was studied in a static system over the temperature range of 411°–471°C and a pressure range of 39–202 mm Hg. The reactions in seasoned vessels, with the propene inhibitor always present, were homogen
The elimination kinetics of 2-chloropropionic acid have been studied over the temperature range of 320-370.2"C and pressure range of 79-218.5 torr. The reaction in seasoned vessel and in the presence of the free radical suppressor cyclohexene, is homogeneous, unimolecular, and obeys a first-order ra