## Abstract For Abstract see ChemInform Abstract in Full Text.
Photochemical reaction of friedelin with acetone
β Scribed by Hidekazu Shirasaki; Takahiko Tsuyuki; Takeyoshi Takahashi; Robert Stevenson
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- French
- Weight
- 205 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract The enol of acetone, formed by disproportionation reactions of 1βhydroxyβ1βmethylethyl radicals, is detected by NMR, spectroscopy during photoreactions of 3βhydroxyβ3βmethylβ2βbutanone in acetonitrile and of acetone in 2βpropanol and slowly tautomerizes to acetone. The photolysis of 3βh
Nitrogen tetroxide, a powerful oxidizing agent, reacts with nearly all classes of orgtic canpounds under a misty of conditions (1). Generally, little selectivity is observed in these reactions since nitric acid, nitrous acid or lower oxides of nitrogen are produced in the primary reactions and insti
Gas-liquid reactions can be activated by high energy radiations (photons). When gas absorption is accompanied by pseudo-first order reaction further enhancement in the specific rate of absorption can be realiscd for situations where either the reactive species in the liquid phase is activated or the
## Abstract The reactions of acetone with tellurium tetrachloride have been studied with the aid of proton, carbonβ13, and telluriumβ125 NMR spectroscopy. In the absence of a proton scavenger, such as sodium hydrogen carbonate, at ambient temperature, a 2 : 1 ratio of acetone to tellurium tetrachlo