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  2. Acetone - Wikipedia

    en.wikipedia.org/wiki/Acetone

    Acetone is a weak Lewis base that forms adducts with soft acids like I 2 and hard acids like phenol. Acetone also forms complexes with divalent metals. [48] [49] Under ultraviolet light, acetone fluoresces.. [50] The flame temperature of pure acetone is 1980 °C. [51]

  3. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    The most common Lewis bases are anions. The strength of Lewis basicity correlates with the pK a of the parent acid: acids with high pK a 's give good Lewis bases. As usual, a weaker acid has a stronger conjugate base. Examples of Lewis bases based on the general definition of electron pair donor include: simple anions, such as H − and F −

  4. 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.

  5. Structural formula - Wikipedia

    en.wikipedia.org/wiki/Structural_formula

    Lewis structures (or "Lewis dot structures") are flat graphical formulas that show atom connectivity and lone pair or unpaired electrons, but not three-dimensional structure. This notation is mostly used for small molecules. Each line represents the two electrons of a single bond. Two or three parallel lines between pairs of atoms represent ...

  6. Acetone (data page) - Wikipedia

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

    Structure and properties Index of refraction, n D: 1.3561 Dielectric constant, ... Vapor pressure of acetone based on formula, = + from ...

  7. 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 ...

  8. Ketone - Wikipedia

    en.wikipedia.org/wiki/Ketone

    In organic chemistry, a ketone / ˈ k iː t oʊ n / is an organic compound with the structure R−C(=O)−R', where R and R' can be a variety of carbon-containing substituents. Ketones contain a carbonyl group −C(=O)− (a carbon-oxygen double bond C=O). The simplest ketone is acetone (where R and R' is methyl), with the formula (CH 3) 2 CO ...

  9. Enolate - Wikipedia

    en.wikipedia.org/wiki/Enolate

    In addition to the use of strong bases, enolates can be generated using a Lewis acid and a weak base ("soft conditions"): For deprotonation to occur, the stereoelectronic requirement is that the alpha-C-H sigma bond must be able to overlap with the pi* orbital of the carbonyl: Stereoelectronic deprotonation requirements