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  2. Schmidt reaction - Wikipedia

    en.wikipedia.org/wiki/Schmidt_reaction

    RXNO:0000170. In organic chemistry, the Schmidt reaction is an organic reaction in which an azide reacts with a carbonyl derivative, usually an aldehyde, ketone, or carboxylic acid, under acidic conditions to give an amine or amide, with expulsion of nitrogen. [1][2][3] It is named after Karl Friedrich Schmidt (1887–1971), who first reported ...

  3. Wurtz–Fittig reaction - Wikipedia

    en.wikipedia.org/wiki/Wurtz–Fittig_reaction

    The Wurtz–Fittig reaction is the chemical reaction of an aryl halide, alkyl halides, and sodium metal to give substituted aromatic compounds. [1] Following the work of Charles Adolphe Wurtz on the sodium-induced coupling of alkyl halides (the Wurtz reaction), Wilhelm Rudolph Fittig extended the approach to the coupling of an alkyl halide with an aryl halide.

  4. Gattermann reaction - Wikipedia

    en.wikipedia.org/wiki/Gattermann_reaction

    Gattermann reaction. The Gattermann reaction (also known as the Gattermann formylation and the Gattermann salicylaldehyde synthesis) is a chemical reaction in which aromatic compounds are formylated by a mixture of hydrogen cyanide (HCN) and hydrogen chloride (HCl) in the presence of a Lewis acid catalyst such as aluminium chloride (AlCl 3). [1 ...

  5. Schotten–Baumann reaction - Wikipedia

    en.wikipedia.org/wiki/Schotten–Baumann_reaction

    The Schotten–Baumann reaction is a method to synthesize amides from amines and acid chlorides: An example of a Schotten-Baumann reaction. Benzylamine reacts with acetyl chloride under Schotten-Baumann conditions to form N -benzylacetamide. Schotten–Baumann reaction also refers to the conversion of acid chloride to esters.

  6. Briggs–Rauscher reaction - Wikipedia

    en.wikipedia.org/wiki/Briggs–Rauscher_reaction

    Oscillogram made in July 1972 by Briggs and Rauscher. The Briggs–Rauscher oscillating reaction is one of a small number of known oscillating chemical reactions.It is especially well suited for demonstration purposes because of its visually striking colour changes: the freshly prepared colourless solution slowly turns an amber colour, then suddenly changes to a very dark blue.

  7. Solvolysis - Wikipedia

    en.wikipedia.org/wiki/Solvolysis

    Solvolysis. In chemistry, solvolysis is a type of nucleophilic substitution (S N 1/S N 2) or elimination where the nucleophile is a solvent molecule. [ 1 ] Characteristic of S N 1 reactions, solvolysis of a chiral reactant affords the racemate. Sometimes however, the stereochemical course is complicated by intimate ion pairs, whereby the ...

  8. Hunsdiecker reaction - Wikipedia

    en.wikipedia.org/wiki/Hunsdiecker_reaction

    RXNO:0000106. The Hunsdiecker reaction (also called the Borodin reaction or the Hunsdiecker–Borodin reaction) is a name reaction in organic chemistry whereby silver salts of carboxylic acids react with a halogen to produce an organic halide. [1] It is an example of both a decarboxylation and a halogenation reaction as the product has one ...

  9. Chemical reaction - Wikipedia

    en.wikipedia.org/wiki/Chemical_reaction

    Chemical reaction. A thermite reaction using iron (III) oxide. The sparks flying outwards are globules of molten iron trailing smoke in their wake. A chemical reaction is a process that leads to the chemical transformation of one set of chemical substances to another. [ 1 ] When chemical reactions occur, the atoms are rearranged and the ...