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  2. Chloroethane - Wikipedia

    en.wikipedia.org/wiki/Chloroethane

    Chloroethane, commonly known as ethyl chloride, is a chemical compound with chemical formula CH 3 CH 2 Cl, once widely used in producing tetraethyllead, a gasoline additive. It is a colorless, flammable gas or refrigerated liquid with a faintly sweet odor.

  3. Dehydrohalogenation - Wikipedia

    en.wikipedia.org/wiki/Dehydrohalogenation

    Here ethyl chloride reacts with potassium hydroxide, typically in a solvent such as ethanol, giving ethylene. Likewise, 1-chloropropane and 2-chloropropane give propene . Zaitsev's rule helps to predict regioselectivity for this reaction type.

  4. 1,2-Dichloroethane - Wikipedia

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

    In the laboratory it is occasionally used as a source of chlorine, with elimination of ethene and chloride. Via several steps, 1,2-dichloroethane is a precursor to 1,1,1-trichloroethane . Historically, before leaded petrol was phased out, chloroethanes were used as an additive in petrol to prevent lead buildup in engines.

  5. Hexachloroethane - Wikipedia

    en.wikipedia.org/wiki/Hexachloroethane

    Chlorination of tetrachloroethylene at 100–140 °C with the presence of ferric chloride is the most commonly used commercial production method, however several other methods exist. A high purity form can be produced in a small scale by reacting chlorine together with barium carbide .

  6. Hypothetical types of biochemistry - Wikipedia

    en.wikipedia.org/wiki/Hypothetical_types_of...

    False-color Cassini radar mosaic of Titan's north polar region; the blue areas are lakes of liquid hydrocarbons. "The existence of lakes of liquid hydrocarbons on Titan opens up the possibility for solvents and energy sources that are alternatives to those in our biosphere and that might support novel life forms altogether different from those on Earth."—NASA Astrobiology Roadmap 2008 [1]

  7. Ethyl group - Wikipedia

    en.wikipedia.org/wiki/Ethyl_group

    In organic chemistry, an ethyl group (abbr. Et) is an alkyl substituent with the formula −CH 2 CH 3, derived from ethane (C 2 H 6). Ethyl is used in the International Union of Pure and Applied Chemistry's nomenclature of organic chemistry for a saturated two-carbon moiety in a molecule, while the prefix "eth-" is used to indicate the presence ...

  8. Hildebrand solubility parameter - Wikipedia

    en.wikipedia.org/wiki/Hildebrand_solubility...

    (However, PE only dissolves at temperatures well above 100 °C.) Poly(styrene) has a solubility parameter of 9.1 cal 1/2 cm −3/2, and thus ethyl acetate is likely to be a good solvent. Nylon 6,6 has a solubility parameter of 13.7 cal 1/2 cm −3/2, and ethanol is likely to be the best solvent of those tabulated. However, the latter is polar ...

  9. Tetrachloroethylene - Wikipedia

    en.wikipedia.org/wiki/Tetrachloroethylene

    Oxidation of tetrachloroethylene by ultraviolet radiation in air produces trichloroacetyl chloride and phosgene: 4 C 2 Cl 4 + 3 O 2 → 2 CCl 3 COCl + 4 COCl 2. This reaction can be halted by using amines and phenols (usually N-methylpyrrole and N-methylmorpholine) as stabilisers. But the reaction can be done intentionally to produce ...