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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. Mannich reaction - Wikipedia

    en.wikipedia.org/wiki/Mannich_reaction

    Reactions between aldimines and α-methylene carbonyls are also considered Mannich reactions because these imines form between amines and aldehydes. The reaction is named after Carl Mannich. [2] [3] Scheme 1 – Ammonia or an amine reacts with formaldehyde and an alpha acidic proton of a carbonyl compound to a beta amino carbonyl compound.

  4. Insertion reaction - Wikipedia

    en.wikipedia.org/wiki/Insertion_reaction

    This reaction happens via a SET mechanism ( single-electron-transfer mechanism ). If magnesium reacts with an alkyl halide, it forms a Grignard reagent, or if lithium reacts, an organolithium reagent is formed. Thus, this type of insertion reactions has important applications in chemical synthesis. Insertion reactions of magnesium and lithium

  5. Aminolysis - Wikipedia

    en.wikipedia.org/wiki/Aminolysis

    Another common example is the reaction of a primary amine or secondary amine with a carboxylic acid or with a carboxylic acid derivative to form an amide. This reaction is widely used, especially in the synthesis of peptides. On the simple addition of an amine to a carboxylic acid, a salt of the organic acid and base is obtained.

  6. Ammonia - Wikipedia

    en.wikipedia.org/wiki/Ammonia

    It is the precursor to nitric acid, which is the source for most N-substituted aromatic compounds. Amines can be formed by the reaction of ammonia with alkyl halides or, more commonly, with alcohols: CH 3 OH + NH 3 → CH 3 NH 2 + H 2 O. Its ring-opening reaction with ethylene oxide give ethanolamine, diethanolamine, and triethanolamine.

  7. Magnesium compounds - Wikipedia

    en.wikipedia.org/wiki/Magnesium_compounds

    Magnesium hydride was first prepared in 1951 by the reaction between hydrogen and magnesium under high temperature, pressure and magnesium iodide as a catalyst. [1] It reacts with water to release hydrogen gas; it decomposes at 287 °C, 1 bar: [2] MgH 2 → Mg + H 2. Magnesium can form compounds with the chemical formula MgX 2 (X=F

  8. Koch reaction - Wikipedia

    en.wikipedia.org/wiki/Koch_reaction

    The Koch reaction is an organic reaction for the synthesis of tertiary carboxylic acids from alcohols or alkenes and carbon monoxide. Some commonly industrially produced Koch acids include pivalic acid , 2,2-dimethylbutyric acid and 2,2-dimethylpentanoic acid. [ 1 ]

  9. Magnesium nitride - Wikipedia

    en.wikipedia.org/wiki/Magnesium_nitride

    Magnesium nitride reacts with water to produce magnesium hydroxide and ammonia gas, as do many metal nitrides.. Mg 3 N 2 (s) + 6 H 2 O(l) → 3 Mg(OH) 2 (aq) + 2 NH 3 (g). In fact, when magnesium is burned in air, some magnesium nitride is formed in addition to the principal product, magnesium oxide.