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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. It can exist as either of two geometric isomers, cis-1,2-dichloroethene or trans-1,2-dichloroethene, but is often used as a mixture of the two ...
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 ...
Dichloroethene or dichloroethylene, often abbreviated as DCE, can refer to any one of several isomeric forms of the organochloride with the molecular formula C 2 H 2 Cl 2: There are three isomers: 1,1-Dichloroethylene; 1,2-Dichloroethylene (E and Z)
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The most common use of 1,2-dichloroethane is in the production of vinyl chloride, which is used to make polyvinyl chloride (PVC) pipes, furniture and automobile upholstery, wall coverings, housewares, and automobile parts. [4] 1,2-Dichloroethane is also used generally as an intermediate for other organic chemical compounds, and as a solvent.
The following other wikis use this file: Usage on ca.wikipedia.org Isòmer; Usage on en.wikibooks.org A-level Chemistry/OCR (Salters)/Isomerism; Usage on eo.wikipedia.org Vinila klorido; Usage on et.wikibooks.org Anorgaaniline Keemia/Sümmeetria; Usage on fa.wikipedia.org ۱٬۲-دیکلرواتن; Usage on pt.wikipedia.org 1,2-Dicloroeteno
Index of refraction, [1] n D: 1.4448 Abbe number? Dielectric constant, [2] ε r: 10.5 ε 0 at 20 °C Bond strength? Bond length? Bond angle? Magnetic susceptibility? Surface tension [3] 40.05 mN/m at 10 °C 38.75 mN/m at 20 °C 28.4 mN/m at 100 °C Viscosity [4] 1.1322 mPa·s at 0 °C 0.8385 mPa·s at 20 °C 0.6523 mPa·s at 40 °C 0.4357 mPa ...
1,1,2,2-tetrachloroethane was used in large amounts to produce other chemicals like trichloroethylene, tetrachloroethylene, and 1,2-dichloroethylene. [6] Because of its possible carcinogen effects on humans, the production of 1,1,2,2-tetrachloroethane has decreased significantly and is no longer widely used as an end-product. [7]