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  2. Schiff base - Wikipedia

    en.wikipedia.org/wiki/Schiff_base

    General structure of an imine. Schiff bases are imines in which R 3 is an alkyl or aryl group (not a hydrogen). R 1 and R 2 may be hydrogens General structure of an azomethine compound. In organic chemistry, a Schiff base (named after Hugo Schiff) is a compound with the general structure R 1 R 2 C=NR 3 (R 3 = alkyl or aryl, but not hydrogen).

  3. Imine - Wikipedia

    en.wikipedia.org/wiki/Imine

    A primary imine in which C is attached to both a hydrocarbyl and a H (derived from an aldehyde) is called a primary aldimine; a secondary imine with such groups is called a secondary aldimine. [10] A primary imine in which C is attached to two hydrocarbyls (derived from a ketone) is called a primary ketimine; a secondary imine with such groups ...

  4. Mannich reaction - Wikipedia

    en.wikipedia.org/wiki/Mannich_reaction

    The Schiff base is an electrophile which reacts in a second step in an electrophilic addition with an enol formed from a carbonyl compound containing an acidic alpha-proton. The Mannich reaction is a condensation reaction. [4]: 140 In the Mannich reaction, primary or secondary amines or ammonia react with formaldehyde to form a Schiff base ...

  5. Carbonyl condensation - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_condensation

    Reaction of cyclohexylamine with acetaldehyde forming an imine. Sodium sulfate removes water [1] In organic chemistry, alkylimino-de-oxo-bisubstitution is the organic reaction of carbonyl compounds with amines to imines. [2] The reaction name is based on the IUPAC Nomenclature for Transformations.

  6. Reductive amination - Wikipedia

    en.wikipedia.org/wiki/Reductive_amination

    First, the nickel metal dehydrogenates the alcohol to form a ketone and Ni-H complex. Then, the ketone reacts with ammonia to form an imine. Finally, the imine reacts with Ni-H to regenerate catalyst and form primary amine. An example of a homogeneous catalytic system is the reductive amination of ketones done with an iridium catalyst. [20]

  7. Hemiaminal - Wikipedia

    en.wikipedia.org/wiki/Hemiaminal

    Methanolamine, a simple hemiaminal. The adducts formed by the addition of ammonia to aldehydes have long been studied. [3] Compounds containing both a primary amino group and a hydroxyl group bonded to the same carbon atom are rarely stable, as they tend to dehydrate to form imines which polymerise to hexamethylenetetramine.

  8. Phase diagram - Wikipedia

    en.wikipedia.org/wiki/Phase_diagram

    The pressure on a pressure-temperature diagram (such as the water phase diagram shown above) is the partial pressure of the substance in question. A phase diagram in physical chemistry , engineering , mineralogy , and materials science is a type of chart used to show conditions (pressure, temperature, etc.) at which thermodynamically distinct ...

  9. Oxime - Wikipedia

    en.wikipedia.org/wiki/Oxime

    In organic chemistry, an oxime is an organic compound belonging to the imines, with the general formula RR’C=N−OH, where R is an organic side-chain and R' may be hydrogen, forming an aldoxime, or another organic group, forming a ketoxime. O-substituted oximes form a closely related family of compounds.