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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.
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 .
Because the cis–trans and E–Z systems compare different groups on the alkene, it is not strictly true that Z corresponds to cis and E corresponds to trans. For example, trans-2-chlorobut-2-ene (the two methyl groups, C1 and C4, on the but-2-ene backbone are trans to each other) is (Z)-2-chlorobut-2-ene (the chlorine and C4 are together ...
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)
1,2-Dibromoethane; Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). ...
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1,1-Dibromoethane is a clear, slightly brown, flammable chemical compound. [3] It is classified as the organobromine compound, and has the chemical formula C 2 H 4 Br 2 [4] and it is a position isomer of 1,2-dibromoethane. It is commonly seen in industrial chemistry, where it is used as a fuel additive. [5]