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  2. Propionic acid - Wikipedia

    en.wikipedia.org/wiki/Propionic_acid

    Propionic acid (/ p r oʊ p i ˈ ɒ n ɪ k /, from the Greek words πρῶτος : prōtos, meaning "first", and πίων : píōn, meaning "fat"; also known as propanoic acid) is a naturally occurring carboxylic acid with chemical formula CH 3 CH 2 CO 2 H. It is a liquid with a pungent and unpleasant smell somewhat resembling body odor. The ...

  3. Saturated and unsaturated compounds - Wikipedia

    en.wikipedia.org/wiki/Saturated_and_unsaturated...

    A saturated compound is a chemical compound (or ion) that resists addition reactions, such as hydrogenation, oxidative addition, and binding of a Lewis base. The term is used in many contexts and for many classes of chemical compounds. Overall, saturated compounds are less reactive than unsaturated compounds.

  4. Propionaldehyde - Wikipedia

    en.wikipedia.org/wiki/Propionaldehyde

    Both industrially and in the laboratory, propionaldehyde has primary application as a chemical building block. [2]: 4 [4] It is predominantly used as a precursor to trimethylolethane (CH 3 C(CH 2 OH) 3) through a condensation reaction with formaldehyde. This triol is an important intermediate in the production of alkyd resins.

  5. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    Lewis structure of a water molecule. Lewis structures – also called Lewis dot formulas, Lewis dot structures, electron dot structures, or Lewis electron dot structures (LEDs) – are diagrams that show the bonding between atoms of a molecule, as well as the lone pairs of electrons that may exist in the molecule.

  6. Acetic acid - Wikipedia

    en.wikipedia.org/wiki/Acetic_acid

    acetyl chloride SOCl 2 acetic acid (i) Li[AlH 4], ether (ii) H 3 O + ethanol Two typical organic reactions of acetic acid Acetic acid undergoes the typical chemical reactions of a carboxylic acid. Upon treatment with a standard base, it converts to metal acetate and water. With strong bases (e.g., organolithium reagents), it can be doubly deprotonated to give LiCH 2 COOLi. Reduction of acetic ...

  7. Acetylacetone - Wikipedia

    en.wikipedia.org/wiki/Acetylacetone

    Acetylacetone is an organic compound with the chemical formula CH 3 −C(=O)−CH 2 −C(=O)−CH 3. ... The structure of the acetylacetonate anion ...

  8. Acetyl group - Wikipedia

    en.wikipedia.org/wiki/Acetyl_group

    In organic chemistry, an acetyl group is a functional group denoted by the chemical formula −COCH 3 and the structure −C(=O)−CH 3. It is sometimes represented by the symbol Ac [5] [6] (not to be confused with the element actinium). In IUPAC nomenclature, an acetyl group is called an ethanoyl group.

  9. Pyruvic acid - Wikipedia

    en.wikipedia.org/wiki/Pyruvic_acid

    Pyruvic acid (CH 3 COCOOH) is the simplest of the alpha-keto acids, with a carboxylic acid and a ketone functional group. Pyruvate, the conjugate base, CH 3 COCOO −, is an intermediate in several metabolic pathways throughout the cell.