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  2. Schmidt reaction - Wikipedia

    en.wikipedia.org/wiki/Schmidt_reaction

    The carboxylic acid Schmidt reaction starts with acylium ion 1 obtained from protonation and loss of water. Reaction with hydrazoic acid forms the protonated azido ketone 2 , which goes through a rearrangement reaction with the alkyl group R, migrating over the C-N bond with expulsion of nitrogen.

  3. Carbonyl reduction - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_reduction

    Ketones, aldehydes, carboxylic acids, esters, amides, and acid halides - some of the most pervasive functional groups, -comprise carbonyl compounds. Carboxylic acids, esters, and acid halides can be reduced to either aldehydes or a step further to primary alcohols , depending on the strength of the reducing agent.

  4. Carbonyl group - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_group

    A ketone compound containing a carbonyl group (C=O) For organic chemistry, a carbonyl group is a functional group with the formula C=O, composed of a carbon atom double-bonded to an oxygen atom, and it is divalent at the C atom.

  5. Ugi reaction - Wikipedia

    en.wikipedia.org/wiki/Ugi_reaction

    These chemical libraries are sets of compounds that can be tested repeatedly. Using the principles of combinatorial chemistry, the Ugi reaction offers the possibility to synthesize a great number of compounds in one reaction, by the reaction of various ketones (or aldehydes), amines, isocyanides and carboxylic acids. These libraries can then be ...

  6. Aldol condensation - Wikipedia

    en.wikipedia.org/wiki/Aldol_condensation

    However, this problem can be avoided if one of the compounds does not contain an α-hydrogen, rendering it non-enolizable. In an aldol condensation between an aldehyde and a ketone, the ketone acts as the nucleophile, as its carbonyl carbon does not possess high electrophilic character due to the +I effect and steric hindrance. Usually, the ...

  7. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    If the compound is a natural product or a carboxylic acid, the prefix oxo-may be used to indicate which carbon atom is part of the aldehyde group; for example, CHOCH 2 COOH is named 2-oxoethanoic acid. If replacing the aldehyde group with a carboxyl group (−COOH) would yield a carboxylic acid with a trivial name, the aldehyde may be named by ...

  8. Nef reaction - Wikipedia

    en.wikipedia.org/wiki/Nef_reaction

    In organic chemistry, the Nef reaction is an organic reaction describing the acid hydrolysis of a salt of a primary or secondary nitroalkane (R−NO 2) to an aldehyde (R−CH=O) or a ketone (R 2 C=O) and nitrous oxide (N 2 O). The reaction has been the subject of several literature reviews. [1] [2] [3] The Nef reaction: 1. Salt of a nitroalkane ...

  9. α-Halo carboxylic acids and esters - Wikipedia

    en.wikipedia.org/wiki/Α-Halo_carboxylic_acids...

    Similarly, the α-bromocarboxylic acid undergo nucleophilic substitution with ammonia to give the amino acid, [3] The Darzens reaction involves a ketone or aldehyde with an α-haloester in the presence of a base to form an α,β-epoxy ester, also called a "glycidic ester". [4] The reaction process begins with deprotonation at the halogenated ...