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  2. Acetone - Wikipedia

    en.wikipedia.org/wiki/Acetone

    Acetone (2-propanone or dimethyl ketone) is an organic compound with the formula (CH 3) 2 CO. [22] It is the simplest and smallest ketone (>C=O).It is a colorless, highly volatile, and flammable liquid with a characteristic pungent odour, very reminiscent of the smell of pear drops.

  3. Acetone (data page) - Wikipedia

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

    Vapor pressure of acetone based on formula, = + from Lange's Handbook of Chemistry, 10th ed. vapor pressure of acetone (log scale) based on formula, log 10 ⁡ P m m H g = 7.02447 − 1161.0 224 + T {\displaystyle \scriptstyle \log _{10}P_{mmHg}=7.02447-{\frac {1161.0}{224+T}}} from Lange's Handbook of Chemistry , 10th ed.

  4. Acetylacetone - Wikipedia

    en.wikipedia.org/wiki/Acetylacetone

    Acetone and acetic anhydride ((CH 3 C(O)) 2 O) upon the addition of boron trifluoride (BF 3) catalyst: [11] (CH 3 C(O)) 2 O + CH 3 C(O)CH 3 → CH 3 C(O)CH 2 C(O)CH 3 A second synthesis involves the base-catalyzed condensation (e.g., by sodium ethoxide CH 3 CH 2 O − Na + ) of acetone and ethyl acetate , followed by acidification of the sodium ...

  5. Ketone - Wikipedia

    en.wikipedia.org/wiki/Ketone

    In aldehydes, the carbonyl is bonded to one carbon and one hydrogen and are located at the ends of carbon chains. Ketones are also distinct from other carbonyl-containing functional groups, such as carboxylic acids, esters and amides. [5] The carbonyl group is polar because the electronegativity of the oxygen is greater than that for carbon.

  6. Deuterated acetone - Wikipedia

    en.wikipedia.org/wiki/Deuterated_acetone

    Deuterated acetone is prepared by the reaction of acetone with heavy water, 2 H 2 O or D 2 O, in the presence of a base. In this case, the base used is deuterated lithium hydroxide : [ 1 ] In order to fully deuterate the acetone, the process is repeated several times, distilling off the acetone from the heavy water, and re-running the reaction ...

  7. Acid dissociation constant - Wikipedia

    en.wikipedia.org/wiki/Acid_dissociation_constant

    pKa values for acetic, chloroacetic, dichloroacetic and trichloroacetic acids. Inductive effects and mesomeric effects affect the pK a values. A simple example is provided by the effect of replacing the hydrogen atoms in acetic acid by the more electronegative chlorine atom.

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  9. 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