N-chloro-3-aminopropanol was obtained in aqueous solution by mixing the amine with the hypochlorite. The first order decomposition kinetics of the N-chloramine in strongly alkaline media are explained by a mechanism in which the rate controlling step is the formation of an imine which is subsequentl
Thermal decomposition of 3-chloro-3-trichloromethyldiazirine in solution
โ Scribed by Michael T. H. Liu; K. Toriyama
- Book ID
- 102443974
- Publisher
- John Wiley and Sons
- Year
- 1972
- Tongue
- English
- Weight
- 225 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0538-8066
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โฆ Synopsis
The thermal decomposition of 3-chloro-3-trichloromethyldizairine in carbon tetrachloride and iso-octane has been investigated over the temperature range 75-1 15OC. The products, tetrachloroethylene and nitrogen, are formed quantitatively by a first-order reaction which is probably unimolecular: CCls N C1 c1 The results yielded the following Arrhenius equations: k (CCI,) = 1013.8*o.2 exp (-29,200 & 200/RT) sec-' k (iso-octane) = 1 0 1 3 . 8 * a . 2 exp (-29,000 f 150/RT) sec-'
๐ SIMILAR VOLUMES
Chlorophenylcarbene reacts with electrophilic olefins to form cyclopropane products in high yield through proposed ylide intermediates. Diazirines, cyclic structural isomers of diazo compounds, are routinely employed as carbene precursors. 1 Although photolytic methods are most commonly used for din