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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. 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 ...

  4. 1,2-Dichloroethane (data page) - Wikipedia

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

    This page was last edited on 19 January 2023, at 06:35 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  5. Talk:1,2-Dichloroethylene - Wikipedia

    en.wikipedia.org/wiki/Talk:1,2-Dichloroethylene

    1,2-Dichloroethene → 1,2-Dichloroethylene; 1,1-Dichloroethene → 1,1-Dichloroethylene; 1,1-Difluoroethene → 1,1-Difluoroethylene – Consistency with trichloroethylene and tetrachloroethylene, also not to confuse with the similar-sounding 1,2-Dichloroethane ⲔⲖⲞⲢⲠⲒⲔⲢⲒⲚ 19:19, 15 April 2024 (UTC) — Relisting.

  6. Dichlorodifluoroethylene - Wikipedia

    en.wikipedia.org/wiki/Dichlorodifluoroethylene

    1,1-Dichloro-2,2-difluoroethylene is a low-boiling liquid that is used a refrigerant. [3] It may also be used as a solvent, but has practical limitations as such, because of its low boiling point (commercial listings, 19 °C; lit. 17 °C).

  7. File:Trans-1,2-dichloroethene-3D-balls.png - Wikipedia

    en.wikipedia.org/wiki/File:Trans-1,2...

    This work has been released into the public domain by its author, Benjah-bmm27.This applies worldwide. In some countries this may not be legally possible; if so: Benjah-bmm27 grants anyone the right to use this work for any purpose, without any conditions, unless such conditions are required by law.

  8. Gauche effect - Wikipedia

    en.wikipedia.org/wiki/Gauche_effect

    The gauche effect is very sensitive to solvent effects, due to the large difference in polarity between the two conformers.For example, 2,3-dinitro-2,3-dimethylbutane, which in the solid state exists only in the gauche conformation, prefers the gauche conformer in benzene solution by a ratio of 79:21, but in carbon tetrachloride, it prefers the anti conformer by a ratio of 58:42. [9]

  9. 1,2-Dichloroethyl acetate - Wikipedia

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

    1,2-Dichloroethyl acetate is a chemical compound used in the making of other organic chemicals. It is a liquid which is either white or resembles water . [ 1 ]