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  2. 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.

  3. Thionyl fluoride - Wikipedia

    en.wikipedia.org/wiki/Thionyl_fluoride

    Thionyl fluoride is the inorganic compound with the formula S O F 2. This colourless gas is mainly of theoretical interest, but it is a product of the degradation of sulfur hexafluoride, an insulator in electrical equipment. The molecule adopts a distorted pyramidal structure, with C s symmetry. The S-O and S-F distances are 1.42 and 1.58 Å ...

  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. Beckmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Beckmann_rearrangement

    The Beckmann rearrangement is often catalyzed by acid; however, other reagents have been known to promote the rearrangement. These include tosyl chloride, thionyl chloride, phosphorus pentachloride, phosphorus pentoxide, triethylamine, sodium hydroxide, trimethylsilyl iodide among others. [3]

  6. SNi - Wikipedia

    en.wikipedia.org/wiki/SNi

    A typical representative organic reaction displaying this mechanism is the chlorination of alcohols with thionyl chloride, or the decomposition of alkyl chloroformates, the main feature is retention of stereochemical configuration. Some examples for this reaction were reported by Edward S. Lewis and Charles E. Boozer in 1952. [2]

  7. Acetyl chloride - Wikipedia

    en.wikipedia.org/wiki/Acetyl_chloride

    Acetyl chloride was first prepared in 1852 by French chemist Charles Gerhardt by treating potassium acetate with phosphoryl chloride. [4]Acetyl chloride is produced in the laboratory by the reaction of acetic acid with chlorodehydrating agents such as phosphorus trichloride (PCl 3), phosphorus pentachloride (PCl 5), sulfuryl chloride (SO 2 Cl 2), phosgene, or thionyl chloride (SOCl 2).

  8. Selenium oxydichloride - Wikipedia

    en.wikipedia.org/wiki/Selenium_oxydichloride

    The SeOCl 2 is generally a labile Lewis acid and solutions of sulfur trioxide in SeOCl 2 likely form [SeOCl] + [SO 3 Cl] − the same way. [ 5 ] The compound hydrolyzes readily to form hydrogen chloride and selenium dioxide , [ citation needed ] and very few organic compounds dissolve in it without reaction.

  9. Lithium tetrachloroaluminate - Wikipedia

    en.wikipedia.org/wiki/Lithium_tetrachloroaluminate

    A solution of lithium tetrachloroaluminate in thionyl chloride is the liquid cathode and electrolyte in those baterries, e.g. the lithium-thionyl chloride cell. Another cathode-electrolyte formulation is lithium tetrachloroaluminate + thionyl chloride + sulfur dioxide + bromine.