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  2. Acetone - Wikipedia

    en.wikipedia.org/wiki/Acetone

    A variety of organic reactions employ acetone as a polar, aprotic solvent, e.g. the Jones oxidation. Because acetone is cheap, volatile, and dissolves or decomposes with most laboratory chemicals, an acetone rinse is the standard technique to remove solid residues from laboratory glassware before a final wash. [66]

  3. Cyanohydrin reaction - Wikipedia

    en.wikipedia.org/wiki/Cyanohydrin_reaction

    In organic chemistry, a cyanohydrin reaction is an organic reaction in which an aldehyde (−CH=O) or ketone (>C=O) reacts with a cyanide anion (N≡C −) or a nitrile (−C≡N) to form a cyanohydrin (>C(OH)C≡N).

  4. Acetone cyanohydrin - Wikipedia

    en.wikipedia.org/wiki/Acetone_cyanohydrin

    Acetone cyanohydrin (ACH) is an organic compound used in the production of methyl methacrylate, the monomer of the transparent plastic polymethyl methacrylate (PMMA), also known as acrylic. It liberates hydrogen cyanide easily, so it is used as a source of such.

  5. Bargellini reaction - Wikipedia

    en.wikipedia.org/wiki/Bargellini_reaction

    The Bargellini reaction is a chemical reaction discovered in 1906 by Italian chemist Guido Bargellini. [1] The original reaction was a mixture of the reagents phenol, chloroform, and acetone in the presence of a sodium hydroxide solution. [2]

  6. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    This can be facilitated by the addition of an organic co-solvent such as dioxane, pyridine, acetone or t-BuOH. KMnO 4 reacts with many functional groups, such as secondary alcohols, 1,2-diols, aldehydes, alkenes, oximes, sulfides and thiols, and carbon-carbon double bonds. Thus, selectivity is an issue.

  7. Cumene process - Wikipedia

    en.wikipedia.org/wiki/Cumene_process

    First stage of Hock process: alkylation of benzene with propylene. Second stage of Hock process: autoxidation of cumene. The cumene process (cumene-phenol process, Hock process) is an industrial process for synthesizing phenol and acetone from benzene and propylene.

  8. Acetone azine - Wikipedia

    en.wikipedia.org/wiki/Acetone_azine

    It can also be produced from acetone (2 eq.), ammonia (2 eq.) and hydrogen peroxide (1 eq.). [4] The first step is the formation of acetone imine, Me 2 C=NH; this is then oxidized by hydrogen peroxide through a complex mechanism to give 3,3-dimethyloxaziridine, which reacts with a further molecule of ammonia to produce acetone hydrazone.

  9. Acetylacetone - Wikipedia

    en.wikipedia.org/wiki/Acetylacetone

    3 Reactions. Toggle Reactions subsection. 3.1 Condensations. ... of acetone and ethyl acetate, followed by acidification of the sodium acetylacetonate (e.g., by ...