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  2. α-Ketol rearrangement - Wikipedia

    en.wikipedia.org/wiki/Α-Ketol_rearrangement

    α-Hydroxy aldehydes have a strong thermodynamic preference for rearrangement to the corresponding ketols in the absence of steric or other factors. Rearrangements of α-hydroxy imines are more difficult to predict because of the small energy differences between isomers. One synthetically useful application of this rearrangement is to the ...

  3. Acyloin - Wikipedia

    en.wikipedia.org/wiki/Acyloin

    The name acyloin is derived from the fact that they are formally derived from reductive coupling of carboxylic acyl groups (−C(=O)OH). [1] They are one of the two main classes of hydroxy ketones , distinguished by the position of the hydroxy group relative to the ketone; in this form, the hydroxy is on the alpha carbon , explaining the ...

  4. Hydroxy ketone - Wikipedia

    en.wikipedia.org/wiki/Hydroxy_ketone

    Alpha- and beta-hydroxy ketones. In organic chemistry, a hydroxy ketone (often referred to simply as a ketol) is a functional group consisting of a ketone (>C=O) flanked by a hydroxyl group (−OH). Chemicals in this group can be classified by the position of the hydroxyl relative to the ketone.

  5. Benedict's reagent - Wikipedia

    en.wikipedia.org/wiki/Benedict's_reagent

    The net reaction between an aldehyde (or an alpha-hydroxy-ketone) and the copper(II) ions in Benedict's solution may be written as: RCHO + 2 Cu 2+ + 5 OH − → RCOO − + Cu 2 O + 3 H 2 O. The hydroxide ions in the equation forms when sodium carbonate dissolves in water. With the citrate included, the reaction becomes:

  6. Dakin oxidation - Wikipedia

    en.wikipedia.org/wiki/Dakin_oxidation

    The Dakin oxidation (or Dakin reaction) is an organic redox reaction in which an ortho- or para-hydroxylated phenyl aldehyde (2-hydroxybenzaldehyde or 4-hydroxybenzaldehyde) or ketone reacts with hydrogen peroxide (H 2 O 2) in base to form a benzenediol and a carboxylate. Overall, the carbonyl group is oxidised, whereas the H 2 O 2 is reduced.

  7. Rubottom oxidation - Wikipedia

    en.wikipedia.org/wiki/Rubottom_oxidation

    In order to synthesize α-hydroxy esters, different oxidants are needed such as NaOCl (see above), lead(IV) acetate, or a hypofluorous acid-acetonitrile (HOF-ACN) complex. [ 1 ] [ 27 ] The Rubottom group found that lead(IV) acetate in DCM or benzene gave good yields of acyclic and cyclic α-hydroxy esters after treatment of the crude reaction ...

  8. Category:Alpha-hydroxy ketones - Wikipedia

    en.wikipedia.org/wiki/Category:Alpha-hydroxy_ketones

    Pages in category "Alpha-hydroxy ketones" The following 5 pages are in this category, out of 5 total. This list may not reflect recent changes. D. Danielone;

  9. Hydroxyacetone - Wikipedia

    en.wikipedia.org/wiki/Hydroxyacetone

    It is an α-hydroxyketone, also called a ketol, and is the simplest hydroxy ketone structure. It is a colorless, distillable liquid. It is a colorless, distillable liquid. Preparation