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1,2-Dibromoethylene can be synthesized by halogenation of acetylene (C 2 H 2) with bromine (Br 2). [1] In order to prevent the formation of tetrahalogenated compounds, acetylene is used in excess, with Br 2 as the limiting reagent.
1,1,2,2-Tetrabromoethane, or simply tetrabromoethane (TBE), is a halogenated hydrocarbon, chemical formula C 2 H 2 Br 4.Although three bromine atoms may bind to one of the carbon atoms creating 1,1,1,2-tetrabromoethane this is not thermodynamically favorable, so in practice tetrabromoethane is equal to 1,1,2,2-tetrabromoethane, where each carbon atom binds two bromine atoms.
1,2-Dibromoethane, also known as ethylene dibromide (EDB), is an organobromine compound with the chemical formula C 2 H 4 Br 2.Although trace amounts occur naturally in the ocean, where it is probably formed by algae and kelp, substantial amounts are produced industrially.
Chemical structures are presented to help readers understand the nature of the titled material. One can subdivide chemical compounds into two main groups: molecules, which includes most organic, polyatomic gases, and organometallic compounds, and nonmolecular species, which includes most purely inorganic compounds.
Dibromoacetylene can be made by reacting 1,1,2-tribromoethylene with potassium hydroxide.This method has a danger of causing explosions. [2]Another way is to react acetylene with phenyl lithium (at −50 °C) to make lithium acetylide, which then reacts with bromine to yield the product.
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1,2-Dichloroethylene or 1,2-DCE is the name for a pair of organochlorine compounds with the molecular formula C 2 H 2 Cl 2.The two compounds are isomers, each being colorless liquids with a sweet odor.
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