## Abstract The product quantum yields in the photolysis of 2,2,4,4βtetramethylβ3βpentanone have been measured in homogeneous solvents of different viscosities, in micellar solutions of cetyltrimethylammonium chloride and sodium dodecyl sulfate, and in dioctadecyl ammonium chloride vesicles. The p
The photolysis of 3-pentanone
β Scribed by E.B. Abuin; M.V. Encina; E.A. Lissi
- Publisher
- Elsevier Science
- Year
- 1972
- Weight
- 702 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0047-2670
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The photolysis of trans-3,4-dimethylcyclopentanone has been studied in the gas phase, principally at 313 nm. However, a few experiments have also been performed using laser sources at 308 and 325 nm. Additionally, experiments were also carried out using the cis isomer. The major products produced by
The reaction of [OH]-with Zpentanone produces two enolate ions, (CH,CH,CH,COCH,]-and [CH,COCHCH,CHJ -, by proton abstraction from C(l) and C(3), respectively. Using deuterium isotopic labelling the fragmentation reactions of each enolate have been delineated for collisional activation at both high (