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  2. Sulfuryl chloride - Wikipedia

    en.wikipedia.org/wiki/Sulfuryl_chloride

    Sulfuryl chloride is not found in nature, as can be inferred from its rapid hydrolysis. Sulfuryl chloride is commonly confused with thionyl chloride, SOCl 2. The properties of these two sulfur oxychlorides are quite different: sulfuryl chloride is a source of chlorine whereas thionyl chloride is a source of chloride ions.

  3. Oxidizing agent - Wikipedia

    en.wikipedia.org/wiki/Oxidizing_agent

    The international pictogram for oxidizing chemicals. Dangerous goods label for oxidizing agents. An oxidizing agent (also known as an oxidant, oxidizer, electron recipient, or electron acceptor) is a substance in a redox chemical reaction that gains or "accepts"/"receives" an electron from a reducing agent (called the reductant, reducer, or electron donor).

  4. Thionyl group - Wikipedia

    en.wikipedia.org/wiki/Thionyl_group

    Thionyl chloride, SOCl 2, is a common reagent used in organic synthesis to convert carboxylic acids to acyl chlorides. In organic chemistry , the thionyl group is known as a sulfoxide group or sulfinyl group, and has the general structure RS(=O)R'.

  5. Sulfur dioxide - Wikipedia

    en.wikipedia.org/wiki/Sulfur_dioxide

    Sulfur dioxide is a mild but useful reducing agent. It is oxidized by halogens to give the sulfuryl halides, such as sulfuryl chloride: SO 2 + Cl 2 → SO 2 Cl 2. Sulfur dioxide is the oxidising agent in the Claus process, which is conducted on a large scale in oil refineries. Here, sulfur dioxide is reduced by hydrogen sulfide to give ...

  6. Sulfur compounds - Wikipedia

    en.wikipedia.org/wiki/Sulfur_compounds

    Sulfur polycations, S 8 2+, S 4 2+ and S 16 2+ are produced when sulfur is reacted with oxidising agents in a strongly acidic solution. [1] The colored solutions produced by dissolving sulfur in oleum were first reported as early as 1804 by C.F. Bucholz, but the cause of the color and the structure of the polycations involved was only ...

  7. Methylphosphonyl dichloride - Wikipedia

    en.wikipedia.org/wiki/Methylphosphonyl_dichloride

    Methylphosphonyl dichloride is produced by oxidation of methyldichlorophosphine, with sulfuryl chloride: [3] CH 3 PCl 2 + SO 2 Cl 2 → CH 3 P(O)Cl 2 + SOCl 2. It can also be produced from a range of methylphosphonates (e.g. dimethyl methylphosphonate) via chlorination with thionyl chloride. Various amines catalyse this process. [4]

  8. Sulfuryl chloride fluoride - Wikipedia

    en.wikipedia.org/wiki/Sulfuryl_chloride_fluoride

    Sulfuryl chloride fluoride is a chemical compound with the formula SO 2 ClF. It is a colorless, easily condensed gas. It is a tetrahedral molecule. Liquified sulfuryl chloride fluoride is employed as a solvent for highly oxidizing compounds. [1]

  9. Thionyl chloride - Wikipedia

    en.wikipedia.org/wiki/Thionyl_chloride

    Thionyl chloride is an inorganic compound with the chemical formula SOCl 2.It is a moderately volatile, colourless liquid with an unpleasant acrid odour.Thionyl chloride is primarily used as a chlorinating reagent, with approximately 45,000 tonnes (50,000 short tons) per year being produced during the early 1990s, [5] but is occasionally also used as a solvent.