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1,2-Dibromoethylene, also known as 1,2-dibromoethene and acetylene dibromide, is a dihalogenated unsaturated compound with one bromine on each of the two carbon atoms. There are two isomers of this compound, cis and trans .
1,2-Dibromoethane has wider applications in the preparation of other organic compounds including those carrying modified diazocine rings [9] and vinyl bromide that is a precursor to some fire retardants. [4] In organic synthesis, 1,2-dibromoethane is used to brominate carbanions and to activate magnesium for certain Grignard reagents.
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Dibromoethane can refer to either of two isomeric organobromides with the molecular formula C 2 H 4 Br 2: 1,1-Dibromoethane (ethylidene dibromide) 1,2-Dibromoethane (ethylene dibromide)
Iodine, methyl iodide, and 1,2-dibromoethane are common activating agents. The use of 1,2-dibromoethane is advantageous as its action can be monitored by the observation of bubbles of ethylene. Furthermore, the side-products are innocuous: Mg + BrC 2 H 4 Br → C 2 H 4 + MgBr 2. The amount of Mg consumed by these activating agents is usually ...
Dibromoethane, referring to either 1,1-Dibromoethane or 1,2-Dibromoethane, both being isomeric organobromides of each other; Dibasic ester, an organic chemical compound; Double-balloon enteroscopy, an endoscopic technique for visualization of the small bowel; Design-basis event, the event which a nuclear facility is built to withstand
Tetraethyllead was supplied for blending with raw gasoline in the form of "Ethyl Fluid", which blended tetraethyllead with the lead scavengers 1,2-dibromoethane and 1,2-dichloroethane. Ethyl fluid contained a dye which would distinguish treated gasoline from untreated gasoline and discourage the diversion of gasoline for other purposes, such as ...
The preparation of EtBr stands as a model for the synthesis of bromoalkanes in general. It is usually prepared by the addition of hydrogen bromide to ethene: H 2 C=CH 2 + HBr → H 3 C-CH 2 Br. Bromoethane is inexpensive and would rarely be prepared in the laboratory.