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  2. Acetone - Wikipedia

    en.wikipedia.org/wiki/Acetone

    Acetone (2-propanone or dimethyl ketone) is an organic compound with the formula (CH 3) 2 CO. [22] ... The synthesis involves the condensation of acetone with phenol:

  3. Cumene process - Wikipedia

    en.wikipedia.org/wiki/Cumene_process

    The cumene process (cumene-phenol process, Hock process) is an industrial process for synthesizing phenol and acetone from benzene and propylene. The term stems from cumene (isopropyl benzene), the intermediate material during the process.

  4. Acetone peroxide - Wikipedia

    en.wikipedia.org/wiki/Acetone_peroxide

    Acetone peroxide (/ æ s ə ˈ t ə ʊ n p ɛr ˈ ɒ k s aɪ d / ⓘ also called APEX and mother of Satan [3] [4]) is an organic peroxide and a primary explosive. It is produced by the reaction of acetone and hydrogen peroxide to yield a mixture of linear monomer and cyclic dimer, trimer, and tetramer forms. The monomer is dimethyldioxirane.

  5. Mesityl oxide - Wikipedia

    en.wikipedia.org/wiki/Mesityl_oxide

    It is prepared by the aldol condensation of acetone to give diacetone alcohol, which readily dehydrates to give this compound. [4] [5] Phorone and isophorone may be formed under the same conditions. Isophorone originates via a Michael addition: Phorone is formed by continued aldol condensation:

  6. Acetoacetic ester synthesis - Wikipedia

    en.wikipedia.org/wiki/Acetoacetic_Ester_Synthesis

    Acetoacetic ester synthesis is a chemical reaction where ethyl acetoacetate is alkylated at the α-carbon to both carbonyl groups and then converted into a ketone, or more specifically an α-substituted acetone. This is very similar to malonic ester synthesis. Acetoacetic ester synthesis equation

  7. Acetylacetone - Wikipedia

    en.wikipedia.org/wiki/Acetylacetone

    A general method of synthesis is to treat a metal salt with acetylacetone in the presence of a base: [12] MB z + z Hacac ⇌ M(acac) z + z BH. Both oxygen atoms bind to the metal to form a six-membered chelate ring. In some cases the chelate effect is so strong that no added base is needed to form the complex.

  8. Baeyer–Drewsen indigo synthesis - Wikipedia

    en.wikipedia.org/wiki/Baeyer–Drewsen_indigo...

    The Baeyer–Drewsen indigo synthesis (1882) is an organic reaction in which indigo is prepared from 2-nitrobenzaldehyde and acetone [1] [2] The reaction was developed by von Baeyer and Viggo Drewsen in 1880 to produce the first synthetic indigo at laboratory scale. This procedure is not used at industrial scale.

  9. Ketogenesis - Wikipedia

    en.wikipedia.org/wiki/Ketogenesis

    Ketogenesis pathway. The three ketone bodies (acetoacetate, acetone, and beta-hydroxy-butyrate) are marked within orange boxes. Ketogenesis is the biochemical process through which organisms produce ketone bodies by breaking down fatty acids and ketogenic amino acids.