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  2. Acetoin - Wikipedia

    en.wikipedia.org/wiki/Acetoin

    Acetoin, also known as 3-hydroxybutanone or acetyl methyl carbinol, is an organic compound with the formula CH 3 CH(OH)C(O)CH 3. It is a colorless liquid with a pleasant, buttery odor. It is chiral .

  3. 3-Hydroxybutanal - Wikipedia

    en.wikipedia.org/wiki/3-Hydroxybutanal

    In organic chemistry, 3-hydroxybutanal (acetaldol, aldol) is an organic compound with the formula CH 3 CH(OH)CH 2 CHO and the structure H 3 C−CH−CH 2 −CH=O. It is classified as an aldol (R−CH(OH)−CHR'−C(=O)−R") and the word "aldol" can refer specifically to 3-hydroxybutanal. It is formally the product of the dimerization of ...

  4. Sodium compounds - Wikipedia

    en.wikipedia.org/wiki/Sodium_compounds

    Sodium metal is highly reducing, with the standard reduction potential for the Na + /Na couple being −2.71 volts, [3] though potassium and lithium have even more negative potentials. [4] The thermal, fluidic, chemical, and nuclear properties of molten sodium metal have caused it to be one of the main coolants of choice for the fast breeder ...

  5. Sodium - Wikipedia

    en.wikipedia.org/wiki/Sodium

    The most important sodium compounds are table salt (NaCl), soda ash (Na 2 CO 3), baking soda (NaHCO 3), caustic soda (NaOH), sodium nitrate (NaNO 3), di- and tri-sodium phosphates, sodium thiosulfate (Na 2 S 2 O 3 ·5H 2 O), and borax (Na 2 B 4 O 7 ·10H 2 O). [24] In compounds, sodium is usually ionically bonded to water and anions and is ...

  6. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    For esters such as ethyl acetate (CH 3 COOCH 2 CH 3), ethyl formate (HCOOCH 2 CH 3) or dimethyl phthalate that are based on common acids, IUPAC recommends use of these established names, called retained names. The "-oate" changes to "-ate." Some simple examples, named both ways, are shown in the figure above.

  7. Sodium oxybate - Wikipedia

    en.wikipedia.org/wiki/Sodium_oxybate

    Sodium oxybate is the sodium salt of γ-hydroxybutyric acid (GHB). Its systematic chemical name is sodium 4-hydroxybutanoate, though synonyms like sodium γ-hydroxybutyrate are commonly used. Its condensed structural formula is HOCH 2 CH 2 CH 2 CO 2 Na (molecular formula: C 4 H 7 NaO 3) and its molar mass is 126.09 g mol −1. It is highly ...

  8. Monosodium acetylide - Wikipedia

    en.wikipedia.org/wiki/Monosodium_acetylide

    It is a derived from acetylene by deprotonation using a sodium base, typically sodium amide. [2] HC≡CH + NaNH 2 → NaC≡CH + NH 3. This compound, a white solid, has been characterized by neutron diffraction, which revealed an Na-C bond and a C≡C bond of 127 pm, which is longer than the C≡C bond length in acetylene itself (120.4 pm). [3]

  9. β-Hydroxybutyric acid - Wikipedia

    en.wikipedia.org/wiki/Β-Hydroxybutyric_acid

    β-Hydroxybutyric acid, also known as 3-hydroxybutyric acid or BHB, is an organic compound and a beta hydroxy acid with the chemical formula CH 3 CH(OH)CH 2 CO 2 H; its conjugate base is β-hydroxybutyrate, also known as 3-hydroxybutyrate. β-Hydroxybutyric acid is a chiral compound with two enantiomers: D-β-hydroxybutyric acid and L-β-hydroxybutyric acid.