enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Carbon tetrachloride - Wikipedia

    en.wikipedia.org/wiki/Carbon_tetrachloride

    Carbon tetrachloride, also known by many other names (such as carbon tet for short and tetrachloromethane, also recognised by the IUPAC), is a chemical compound with the chemical formula CCl 4. It is a non-flammable, dense, colourless liquid with a "sweet" chloroform-like odour that can be detected at low levels.

  3. 1,1,1,3,3,3-Hexachloropropane - Wikipedia

    en.wikipedia.org/wiki/1,1,1,3,3,3-Hexachloropropane

    1,1,1,3,3,3-Hexachloropropane is a compound of chlorine, hydrogen, and carbon, with chemical formula C 3 Cl 6 H 2, specifically Cl 3 C−CH 2 −CCl 3. Its molecule can be described as that of propane with chlorine atoms substituted for the six hydrogen atoms on the extremal carbons.

  4. 1,1,1-Trichloroethane - Wikipedia

    en.wikipedia.org/wiki/1,1,1-Trichloroethane

    1,1,1-Trichloroethane is a fairly potent greenhouse gas with a 100-year global warming potential of 169 relative to carbon dioxide. [18] This is nonetheless less than a tenth that of carbon tetrachloride — which it replaced as a solvent — due to its relatively short atmospheric lifetime of about 5 years. [19]

  5. Trichlorofluoromethane - Wikipedia

    en.wikipedia.org/wiki/Trichlorofluoromethane

    Trichlorofluoromethane can be obtained by reacting carbon tetrachloride with hydrogen fluoride at 435 °C and 70 atm, producing a mixture of trichlorofluoromethane, tetrafluoromethane and dichlorodifluoromethane in a ratio of 77:18:5. The reaction can also be carried out in the presence of antimony(III) chloride or antimony(V) chloride: [8]

  6. Appel reaction - Wikipedia

    en.wikipedia.org/wiki/Appel_reaction

    The Appel reaction is an organic reaction that converts an alcohol into an alkyl chloride using triphenylphosphine and carbon tetrachloride. [1] The use of carbon tetrabromide or bromine as a halide source will yield alkyl bromides, whereas using carbon tetraiodide, methyl iodide or iodine gives alkyl iodides. The reaction is credited to and ...

  7. Wohl–Ziegler bromination - Wikipedia

    en.wikipedia.org/wiki/Wohl–Ziegler_bromination

    The Wohl–Ziegler reaction [1] [2] is a chemical reaction that involves the allylic or benzylic bromination of hydrocarbons using an N-bromosuccinimide and a radical initiator. [3] Best yields are achieved with N-bromosuccinimide in carbon tetrachloride solvent. Several reviews have been published. [4] [5]

  8. Bleach - Wikipedia

    en.wikipedia.org/wiki/Bleach

    The highest level cited for a concentration of carbon tetrachloride (seemingly of highest concern) is 459 micrograms per cubic meter, translating to 0.073 ppm (part per million), or 73 ppb (part per billion). The OSHA-allowable time-weighted average concentration over eight hours is 10 ppm, [30] almost 140 times higher;

  9. Hexachloroethane - Wikipedia

    en.wikipedia.org/wiki/Hexachloroethane

    Hexachloroethane (perchloroethane) is an organochlorine compound with the chemical formula (CCl 3) 2.It is a white or colorless solid at room temperature with a camphor-like odor. [3]