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  2. 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]

  3. 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.

  4. Darzens halogenation - Wikipedia

    en.wikipedia.org/wiki/Darzens_halogenation

    Darzens halogenation is the chemical synthesis of alkyl halides from alcohols via the treatment upon reflux of a large excess of thionyl chloride or thionyl bromide (SOX 2) in the presence of a small amount of a nitrogen base, such as a tertiary amine or pyridine or its corresponding hydrochloride or hydrobromide salt.

  5. Halogenation - Wikipedia

    en.wikipedia.org/wiki/Halogenation

    Chlorine is slightly more selective, but still reacts with most metals and heavier nonmetals. Following the usual trend, bromine is less reactive and iodine least of all. Of the many reactions possible, illustrative is the formation of gold(III) chloride by the chlorination of gold.

  6. Acyl chloride - Wikipedia

    en.wikipedia.org/wiki/Acyl_chloride

    General chemical structure of an acyl chloride. In organic chemistry, an acyl chloride (or acid chloride) is an organic compound with the functional group −C(=O)Cl. Their formula is usually written R−COCl, where R is a side chain. They are reactive derivatives of carboxylic acids (R−C(=O)OH).

  7. Sulfonyl halide - Wikipedia

    en.wikipedia.org/wiki/Sulfonyl_halide

    The intermediate benzenesulfonic acid can be chlorinated with thionyl chloride as well. Benzenesulfonyl chloride, the most important sulfonyl halide, can also be produced by treating sodium benzenesulfonate with phosphorus pentachlorides. [5] Benzenediazonium chloride reacts with sulfur dioxide and copper(I) chloride to give the sulfonyl chloride:

  8. 5 holidays tips for limiting your drink choices to save time ...

    www.aol.com/5-holidays-tips-limiting-drink...

    Avoid the stresses of hosting a holiday party by limiting guest beverage options so you can spend more time focusing on family and friends. Here are 5 tips to help.

  9. 1-Chlorohexane - Wikipedia

    en.wikipedia.org/wiki/1-chlorohexane

    1-Chlorohexane can be obtained by reacting hexyl alcohol with hydrochloric acid or thionyl chloride. Physical properties 1-Chlorohexane is a colorless liquid with an ...