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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. Wacker process - Wikipedia

    en.wikipedia.org/wiki/Wacker_process

    Extractive distillation with water removes the lights ends having lower boiling points than acetaldehyde (chloromethane, chloroethane, and carbon dioxide) at the top, while water and higher-boiling byproducts, such as acetic acid, crotonaldehyde or chlorinated acetaldehydes, are withdrawn together with acetaldehyde at the bottom. [27]

  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. Catalytic reforming - Wikipedia

    en.wikipedia.org/wiki/Catalytic_reforming

    A side reaction is hydrogenolysis, which produces light hydrocarbons of lower value, such as methane, ethane, propane and butanes. Continuous Catalytic reforming (CCR) unit In addition to a gasoline blending stock, reformate is the main source of aromatic bulk chemicals such as benzene , toluene , xylene and ethylbenzene , which have diverse ...

  6. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  7. Ethylene oxide - Wikipedia

    en.wikipedia.org/wiki/Ethylene_oxide

    Ethylene oxide is a colorless gas at 25 °C (77 °F) and is a mobile liquid at 0 °C (32 °F) – viscosity of liquid ethylene oxide at 0 °C is about 5.5 times lower than that of water. The gas has a characteristic sweet odor of ether, noticeable when its concentration in air exceeds 500 ppm. [ 26 ]

  8. Vinyl chloride - Wikipedia

    en.wikipedia.org/wiki/Vinyl_chloride

    Numerous attempts have been made to convert ethane directly to vinyl chloride. [2] Ethane, which is even more readily available than ethylene, is a potential precursor to vinyl chloride. The conversion of ethane to vinyl chloride has been demonstrated by various routes: [2] High-temperature chlorination: H 3 C−CH 3 + 2 Cl 2 → H 2 C=CHCl + 3 HCl

  9. 2-Chloroethyl ethyl sulfide - Wikipedia

    en.wikipedia.org/wiki/2-Chloroethyl_ethyl_sulfide

    2-Chloroethyl ethyl sulfide is the organosulfur compound with the formula C 2 H 5 SC 2 H 4 Cl. It is a colorless liquid. It is a colorless liquid. The compound is part of the family of vesicant compounds known as half mustards , has been heavily investigated because of its structural similarity to the sulfur mustard S(C 2 H 4 Cl) 2 .

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