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  2. Butyraldehyde - Wikipedia

    en.wikipedia.org/wiki/Butyraldehyde

    Butyraldehyde is produced almost exclusively by the hydroformylation of propylene: . CH 3 CH=CH 2 + H 2 + CO → CH 3 CH 2 CH 2 CHO. Traditionally, hydroformylation was catalyzed by cobalt carbonyl but rhodium complexes are more common.

  3. Propionaldehyde - Wikipedia

    en.wikipedia.org/wiki/Propionaldehyde

    Propionaldehyde may also be prepared by oxidizing 1-propanol with a mixture of sulfuric acid and potassium dichromate.The reflux condenser contains water heated at 60 °C, which condenses unreacted propanol, but allows propionaldehyde to pass.

  4. Propionic anhydride - Wikipedia

    en.wikipedia.org/wiki/Propionic_anhydride

    Industrial route to propionic anhydride involves thermal dehydration of propionic acid, driving off the water by distillation: . 2 CH 3 CH 2 CO 2 H → (CH 3 CH 2 CO) 2 O + H 2 O ...

  5. 1-Propanol - Wikipedia

    en.wikipedia.org/wiki/1-Propanol

    1-Propanol (also propan-1-ol, propanol, n-propyl alcohol) is a primary alcohol with the formula CH 3 CH 2 CH 2 OH and sometimes represented as PrOH or n-PrOH.It is a colourless liquid and an isomer of 2-propanol. 1-Propanol is used as a solvent in the pharmaceutical industry, mainly for resins and cellulose esters, and, sometimes, as a disinfecting agent.

  6. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    IUPAC name: Common name: Structural formula Propionic acid: propanoic acid ethanecarboxylic acid CH 3 CH 2 CO 2 H : Acrylic acid: propenoic acid acroleic acid ethylenecarboxylic acid

  7. CH3CH2CHO - Wikipedia

    en.wikipedia.org/?title=CH3CH2CHO&redirect=no

    From Wikipedia, the free encyclopedia. Redirect page

  8. 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.

  9. 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.