The reduction of benzophenone by lithium alkoxides gives rise to benzophenone ketyl which disappears in a first-order fashion and whose first-order rate constant is approximately equal to the pseudo-first-order rate constant for the formation of the product, benzhydrol.
β¦ LIBER β¦
Evidence for a two steps electron transfer in the electrochemical reduction of dibromodifluoromethane at carbon
β Scribed by A. Medaghri-Alaoui; H. Choukroun; P. Calas; C. Amatore; A. Commeyras
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 42 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0022-1139
No coin nor oath required. For personal study only.
β¦ Synopsis
In the presence of ethyl acrylate the height of the peak reduction of CF& (PI") is lowered (Pl). The ratio Pt/Pt" can be reduced to 112. depending with concentration of the olefin and speed of the cathodic scan.
π SIMILAR VOLUMES
Evidence for a single electron transfer
β
E.C. Ashby; J.N. Argyropoulos
π
Article
π
1986
π
Elsevier Science
π
French
β 273 KB
βTwo-Electron Reductionβ of Phosphane-su
β
Dipl.-Chem. Klaus Hinkelmann; Falko Mahlendorf; Priv.-Doz. Dr. JΓΌrgen Heinze; Di
π
Article
π
1987
π
John Wiley and Sons
π
English
β 368 KB
π 1 views
Reduction by a model of nad(p)h. 42. Dir
β
Shinro Yasui; Kaoru Nakamura; Atsuyoshi Ohno
π
Article
π
1983
π
Elsevier Science
π
French
β 264 KB
Evidence supporting a single electron tr
β
E.C. Ashby; Anil B. Goel; John N. Argyropoulos
π
Article
π
1982
π
Elsevier Science
π
French
β 215 KB
Ring opening in the reaction of diphenyl
β
Gernot Boche; Michael Marsch
π
Article
π
1983
π
Elsevier Science
π
French
β 238 KB
The reaction of cyclopropanes like 2,3,4-triphenyl-endo-tricyclo[3.2.1.02'0]octane (la) with base is initiated by proton and not by ele$trov transfer. The facile disrotatory cyclopropyl anion ring opening reaction of 2JR2=CN, M =Ll ) at -75Β°C does not occur synchronously. 2,3,4-Triphenyl-endo-tricyc