The mechanism for elimination of acetic acid from 1-acetoxy- and 2-acetoxytetralin
โ Scribed by Stanley F. Wojinski; Michael L. Gross
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 550 KB
- Volume
- 14
- Category
- Article
- ISSN
- 1076-5174
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
The elimination of acetic acid from the MH(+) ions of acetates of stereoisomeric 2-methyl-1-cyclohexanols and 1-hydroxy-trans-decalins exhibits a significant degree of stereospecificity under isobutane chemical ionization and collision-induced dissociation (CID) conditions, resulting in more abundan
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
## Abstract Protonated 4,5โdiacetoxyphenanthrene and 2,2โฒโdiacetoxybiphenyl dissociate, owing to the interaction of the two acetoxy groups, by eliminating a molecule of acetic acid. This novel proximity effect, which occurs for a fast atom bombardmentโproduced closedโshell ion, was examined in deta