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  2. Dichloroacetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Dichloroacetaldehyde

    The compound decomposes when heated. In the presence of Lewis acids such as antimony trichloride, iron(III) chloride, aluminum trichloride, tin(IV) chloride or boron trifluoride, the trimer hexachloroparaldehyde (2,4,6-tris(dichloromethyl)-1,3,5-trioxane) can be obtained. [1] The trimer forms colourless crystals that melt at 131–132 °C.

  3. 2-Chloroethanol - Wikipedia

    en.wikipedia.org/wiki/2-Chloroethanol

    2-Chloroethanol is toxic with an LD 50 of 89 mg/kg in rats. Like most organochlorine compounds, chloroethanol releases hydrochloric acid and phosgene when burned.. In regards to dermal exposure to 2-chloroethanol, the Occupational Safety and Health Administration has set a permissible exposure limit of 5 ppm (16 mg/m 3) over an eight-hour time-weighted average, while the National Institute for ...

  4. 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 ...

  5. Chloral - Wikipedia

    en.wikipedia.org/wiki/Chloral

    Chloral was first prepared, and named, by the German chemist Justus von Liebig in 1832. [2] Liebig treated anhydrous ethanol with dry chlorine gas. [3] Chloral is produced commercially by the chlorination of acetaldehyde in the presence of hydrochloric acid, producing chloral hydrate. Ethanol can also be used as a feedstock.

  6. Dichloroethane - Wikipedia

    en.wikipedia.org/wiki/Dichloroethane

    Dichloroethane can refer to either of two isomeric organochlorides with the molecular formula C 2 H 4 Cl 2: 1,1-Dichloroethane (ethylidene chloride) 1,2-Dichloroethane (ethylene dichloride)

  7. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    An acyclic alkyl has the general formula of −C n H 2n+1. A cycloalkyl group is derived from a cycloalkane by removal of a hydrogen atom from a ring and has the general formulaC n H 2n−1. [2] Typically an alkyl is a part of a larger molecule. In structural formulae, the symbol R is used to designate a generic (unspecified) alkyl group.

  8. 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-Dichloroethene; 1,2-Dichloroethene (E and Z)

  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 ]