Kinetics, isotope rate effect, and mechanism of dehydrobromination of cis-1, 2-dibromoethylene with triethylamine in dimethylformamide
WK Kwok, WG Lee, SI Miller
Index: Kwok,W.K. et al. Journal of the American Chemical Society, 1969 , vol. 91, p. 468 - 476
Full Text: HTML
Citation Number: 16
Abstract
Abstract: The reaction between cis-dibromoethylene and triethylamine in dimethylformamide (DMF) is one of elimination rather than displacement. The probable first product is monobromoacetylene. The activation parameters for this second-order reaction are AH*= 18.1 kcal/mol and AS*=-32 eu. The isotopeeffectforelimina-tion is kI,/kD= 1.00, and there is neither rate retardation nor hydrogen exchange with cis-dibromoethylene, when ...
Related Articles:
[Galy, Nicolas; Doucet, Henri; Santelli, Maurice Tetrahedron Letters, 2010 , vol. 51, # 4 p. 695 - 697]
[Okamoto,Y. et al. Journal of Organic Chemistry, 1972 , vol. 37, p. 3185 - 3187]
[Gaoni, Yehiel; Sadeh, Shoshana Journal of Organic Chemistry, 1980 , vol. 45, # 5 p. 870 - 881]
[McDonald, Stephen A.; Johnson, Gary L.; Keelan, Brian W.; Andrews, Lester Journal of the American Chemical Society, 1980 , vol. 102, # 9 p. 2892 - 2896]
[Nef Justus Liebigs Annalen der Chemie, 1899 , vol. 308, p. 325 Full Text Show Details Fontaine Justus Liebigs Annalen der Chemie, 1870 , vol. 156, p. 260 Full Text Show Details Reboul Justus Liebigs Annalen der Chemie, 1863 , vol. 125, p. 86]