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  2. 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.

  3. Mitsunobu reaction - Wikipedia

    en.wikipedia.org/wiki/Mitsunobu_reaction

    The reaction mechanism of the Mitsunobu reaction is fairly complex. The identity of intermediates and the roles they play has been the subject of debate. Initially, the triphenyl phosphine (2) makes a nucleophilic attack upon diethyl azodicarboxylate (1) producing a betaine intermediate 3, which deprotonates the carboxylic acid (4) to form the ion pair 5.

  4. Ester - Wikipedia

    en.wikipedia.org/wiki/Ester

    Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials, and often have a pleasant characteristic, fruity odor. This leads to their extensive use in the fragrance and flavor industry.

  5. Schmidt reaction - Wikipedia

    en.wikipedia.org/wiki/Schmidt_reaction

    Reaction mechanism for the amine formation from a carboxylic acid via Schmidt reaction. In the reaction mechanism for the Schmidt reaction of ketones, the carbonyl group is activated by protonation for nucleophilic addition by the azide, forming azidohydrin 3, which loses water in an elimination reaction to diazoiminium 5.

  6. Jones oxidation - Wikipedia

    en.wikipedia.org/wiki/Jones_oxidation

    The reaction stoichiometry implicates the Cr(IV) species "CrO 2 OH −", which comproportionates with the chromic acid to give a Cr(V) oxide, which also functions as an oxidant for the alcohol. [ 6 ] The oxidation of the aldehydes is proposed to proceed via the formation of hemiacetal -like intermediates, which arise from the addition of the O ...

  7. Organosulfate - Wikipedia

    en.wikipedia.org/wiki/Organosulfate

    Generic structure of an organosulfate, where R is an organyl group. In organosulfur chemistry, organosulfates are a class of organic compounds sharing a common functional group with the structure R−O−SO − 3. The SO 4 core is a sulfate group and the R group is any organic residue.

  8. Ester hydrolysis - Wikipedia

    en.wikipedia.org/wiki/Ester_hydrolysis

    Alkaline hydrolysis of esters is also known as saponification. A base such as sodium hydroxide is required in stochiometric amounts. Unlike acid-catalyzed ester hydrolysis, it is not an equilibrium reaction and proceeds to completion. Hydroxide ion attacks the carbonyl carbon to give a tetrahedral intermediate, which then expels an alkoxide ion.

  9. Friedel–Crafts reaction - Wikipedia

    en.wikipedia.org/wiki/Friedel–Crafts_reaction

    This reaction is related to several classic named reactions: The acylated reaction product can be converted into the alkylated product via a Clemmensen or a Wolff-Kishner reduction. [17] The Gattermann–Koch reaction can be used to synthesize benzaldehyde from benzene. [18] The Gatterman reaction describes arene reactions with hydrocyanic acid ...