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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. Butyraldehyde - Wikipedia

    en.wikipedia.org/wiki/Butyraldehyde

    Butyraldehyde undergoes reactions typical of alkyl aldehydes, and these define many of the uses of this compound.Important reactions include hydrogenation to the alcohol, oxidation to the acid, and base-catalyzed condensation.

  4. Butanone (data page) - Wikipedia

    en.wikipedia.org/wiki/Butanone_(data_page)

    533 K (260 °C), 4.002 MPa Std enthalpy change of fusion, Δ fus H o: 8.44 kJ/mol Std entropy change of fusion, Δ fus S o: 44.98 J/(mol·K) Std enthalpy change of vaporization, Δ vap H o: 32.2 kJ/mol Std entropy change of vaporization, Δ vap S o: 91.6 J/(mol·K) Solid properties Std enthalpy change of formation, Δ f H o solid? kJ/mol ...

  5. Acetoin - Wikipedia

    en.wikipedia.org/wiki/Acetoin

    Acetoin is a neutral, four-carbon molecule used as an external energy store by a number of fermentative bacteria. It is produced by the decarboxylation of alpha-acetolactate, a common precursor in the biosynthesis of branched-chain amino acids.

  6. Chemosynthesis - Wikipedia

    en.wikipedia.org/wiki/Chemosynthesis

    Venenivibrio stagnispumantis gains energy by oxidizing hydrogen gas.. In biochemistry, chemosynthesis is the biological conversion of one or more carbon-containing molecules (usually carbon dioxide or methane) and nutrients into organic matter using the oxidation of inorganic compounds (e.g., hydrogen gas, hydrogen sulfide) or ferrous ions as a source of energy, rather than sunlight, as in ...

  7. Piceol - Wikipedia

    en.wikipedia.org/wiki/Piceol

    [4] Anticonvulsants are also possible by Mannich reaction: [5] Metabolism. Diprenylated derivatives of piceol can be isolated from Ophryosporus macrodon. [6] 4- ...

  8. Benson group increment theory - Wikipedia

    en.wikipedia.org/wiki/Benson_group_increment_theory

    For 2-butanone going to 2-butanol, enthalpy of reaction is −13.75 kcal/mol, which again is in excellent agreement with −14.02 kcal/mol. While both reactions are thermodynamically favored, the alkene will be far more exothermic than the corresponding ketone.

  9. 1-Butanol - Wikipedia

    en.wikipedia.org/wiki/1-Butanol

    1-Butanol, also known as butan-1-ol or n-butanol, is a primary alcohol with the chemical formula C 4 H 9 OH and a linear structure. Isomers of 1-butanol are isobutanol, butan-2-ol and tert-butanol. The unmodified term butanol usually refers to the straight chain isomer.