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  2. 1,2-Dichloroethylene - Wikipedia

    en.wikipedia.org/wiki/1,2-dichloroethylene

    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 ...

  3. Tetrachloroethylene - Wikipedia

    en.wikipedia.org/wiki/Tetrachloroethylene

    ClCH 2 CH 2 Cl + 3 Cl 2 → Cl 2 C=CCl 2 + 4 HCl. This reaction can be catalyzed by a mixture of potassium chloride and aluminium chloride or by activated carbon. Trichloroethylene is a major byproduct, which is separated by distillation. Worldwide production was about 1 million metric tons (980,000 long tons; 1,100,000 short tons) in 1985. [11]

  4. List of character tables for chemically important 3D point ...

    en.wikipedia.org/wiki/List_of_character_tables...

    These groups are characterized by i) an n-fold proper rotation axis C n; ii) n 2-fold proper rotation axes C 2 normal to C n; iii) a mirror plane σ h normal to C n and containing the C 2 s. The D 1h group is the same as the C 2v group in the pyramidal groups section. The D 8h table reflects the 2007 discovery of errors in older references. [4]

  5. Dichloroethene - Wikipedia

    en.wikipedia.org/wiki/Dichloroethene

    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

  6. 1,2-Dichloroethane - Wikipedia

    en.wikipedia.org/wiki/1,2-Dichloroethane

    The chemical compound 1,2-dichloroethane, commonly known as ethylene dichloride (EDC), is a chlorinated hydrocarbon. It is a colourless liquid with a chloroform -like odour . 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 ...

  7. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cis–trans_isomerism

    In the Benson heat of formation group additivity dataset, cis isomers suffer a 1.10 kcal/mol stability penalty. Exceptions to this rule exist, such as 1,2-difluoroethylene, 1,2-difluorodiazene (FN=NF), and several other halogen- and oxygen-substituted ethylenes.

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  9. 1,2-Dichloroethane (data page) - Wikipedia

    en.wikipedia.org/wiki/1,2-Dichloroethane_(data_page)

    log 10 of 1,2-dichloroethane vapor pressure. Uses formula: log e ⁡ P m m H g = {\displaystyle \scriptstyle \log _{e}P_{mmHg}=} log e ⁡ ( 760 101.325 ) − 10.38248 log e ⁡ ( T + 273.15 ) − 6904.904 T + 273.15 + 83.96795 + 8.368130 × 10 − 6 ( T + 273.15 ) 2 {\displaystyle \scriptstyle \log _{e}({\frac {760}{101.325}})-10.38248\log _{e ...