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  2. Butanone - Wikipedia

    en.wikipedia.org/wiki/Butanone

    Butanone, also known as methyl ethyl ketone (MEK) or ethyl methyl ketone, [a] is an organic compound with the formula CH 3 C(O)CH 2 CH 3.This colorless liquid ketone has a sharp, sweet odor reminiscent of acetone.

  3. Methoxyethane - Wikipedia

    en.wikipedia.org/wiki/Methoxyethane

    Methoxyethane, also known as ethyl methyl ether, is a colorless gaseous ether with the formula CH 3 OCH 2 CH 3.Unlike the related dimethyl ether and diethyl ether, which are widely used and studied, this mixed alkyl ether has no current applications.

  4. Methyl propionate - Wikipedia

    en.wikipedia.org/wiki/Methyl_propionate

    Condensation of Methyl propionate with formaldehyde followed by dehydration yields methyl methacrylate: [4]. MeO 2 CCH 2 CH 3 + CH 2 O → MeO 2 CCH(CH 2 OH)CH 3 MeO 2 CCH(CH 2 OH)CH 3 → MeO 2 CC(=CH 2)CH 3

  5. 3-Pentanone - Wikipedia

    en.wikipedia.org/wiki/3-Pentanone

    It can also be prepared by combining ethylene, CO, and H 2. [4] When the reaction is catalyzed by dicobalt octacarbonyl, water can be used as a source of hydrogen.A proposed intermediate is the ethylene-propionyl species [CH 3 C(O)Co(CO) 3 (ethylene)] which undergoes a migratory insertion to form [CH 3 COCH 2 CH 2 Co(CO) 3].

  6. Methyl acetate - Wikipedia

    en.wikipedia.org/wiki/Methyl_acetate

    Methyl acetate, also known as MeOAc, acetic acid methyl ester or methyl ethanoate, is a carboxylate ester with the formula CH 3 COOCH 3.It is a flammable liquid with a characteristically pleasant smell reminiscent of some glues and nail polish removers.

  7. Propionyl chloride - Wikipedia

    en.wikipedia.org/wiki/Propionyl_chloride

    Propionyl chloride (also propanoyl chloride) is the organic compound with the formula CH 3 CH 2 C(O)Cl. It is the acyl chloride derivative of propionic acid.It undergoes the characteristic reactions of acyl chlorides. [1]

  8. Haloform reaction - Wikipedia

    en.wikipedia.org/wiki/Haloform_reaction

    In chemistry, the haloform reaction (also referred to as the Lieben haloform reaction) is a chemical reaction in which a haloform (CHX 3, where X is a halogen) is produced by the exhaustive halogenation of an acetyl group (R−C(=O)CH 3, where R can be either a hydrogen atom, an alkyl or an aryl group), in the presence of a base.

  9. Williamson ether synthesis - Wikipedia

    en.wikipedia.org/wiki/Williamson_ether_synthesis

    Ether synthesis by reaction of salicylaldehyde with chloroacetic acid and sodium hydroxide [1]. The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol ().