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  2. Acid anhydride - Wikipedia

    en.wikipedia.org/wiki/Acid_anhydride

    An acid anhydride is a type of chemical compound derived by the removal of water molecules from an acid. In organic chemistry, organic acid anhydrides contain the functional group −C(=O)−O−C(=O)−. Organic acid anhydrides often form when one equivalent of water is removed from two equivalents of an organic acid in a dehydration reaction.

  3. Acetic anhydride - Wikipedia

    en.wikipedia.org/wiki/Acetic_anhydride

    Acetic anhydride, or ethanoic anhydride, is the chemical compound with the formula (CH 3 CO) 2 O. Commonly abbreviated Ac 2 O, it is the simplest isolable anhydride of a carboxylic acid and is widely used as a reagent in organic synthesis. It is a colorless liquid that smells strongly of acetic acid, which is formed by its reaction with ...

  4. Organic acid anhydride - Wikipedia

    en.wikipedia.org/wiki/Organic_acid_anhydride

    A common type of organic acid anhydride is a carboxylic anhydride, where the parent acid is a carboxylic acid, the formula of the anhydride being (RC(O)) 2 O. Symmetrical acid anhydrides of this type are named by replacing the word acid in the name of the parent carboxylic acid by the word anhydride. [2] Thus, (CH 3 CO) 2 O is called acetic ...

  5. Maleic anhydride - Wikipedia

    en.wikipedia.org/wiki/Maleic_anhydride

    Maleic anhydride is a classic substrate for Diels-Alder reactions. [9] It was used for work in 1928, on the reaction between maleic anhydride and 1,3-butadiene, for which Otto Paul Hermann Diels and Kurt Alder were awarded the Nobel Prize in 1950. It is through this reaction that maleic anhydride is converted to many pesticides and pharmaceuticals.

  6. Trifluoroacetic anhydride - Wikipedia

    en.wikipedia.org/wiki/Trifluoroacetic_anhydride

    Trifluoroacetic anhydride has various uses in organic synthesis. It may be used to introduce the corresponding trifluoroacetyl group, for which it is more convenient than the corresponding acyl chloride , trifluoroacetyl chloride , which is a gas.

  7. List of reagents - Wikipedia

    en.wikipedia.org/wiki/List_of_reagents

    strong mineral acid; applications include its use as a dehydrating agent in many chemical reactions, sulfonation, the purification of hydrocarbons, and the production of phosphoric acid tert-Butyl hydroperoxide: used in a variety of oxidation processes; industrially, is used as a starter of radical polymerization: Tetrahydrofuran

  8. Anhydrous - Wikipedia

    en.wikipedia.org/wiki/Anhydrous

    To prevent this, anhydrous solvents must be used when performing certain reactions. Examples of reactions requiring the use of anhydrous solvents are the Grignard reaction and the Wurtz reaction. Solvents have typically been dried using distillation or by reaction with reactive metals or metal hydrides. These methods can be dangerous and are a ...

  9. Hydrolase - Wikipedia

    en.wikipedia.org/wiki/Hydrolase

    An example of crucial esterase is acetylcholine esterase, which assists in transforming the neuron impulse into the acetate group after the hydrolase breaks the acetylcholine into choline and acetic acid. [1] Acetic acid is an important metabolite in the body and a critical intermediate for other reactions such as glycolysis.