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  2. Birch reduction - Wikipedia

    en.wikipedia.org/wiki/Birch_reduction

    The Birch reduction is an organic reaction that is used to convert arenes to 1,4-cyclohexadienes.The reaction is named after the Australian chemist Arthur Birch and involves the organic reduction of aromatic rings in an amine solvent (traditionally liquid ammonia) with an alkali metal (traditionally sodium) and a proton source (traditionally an alcohol).

  3. Ammonia solution - Wikipedia

    en.wikipedia.org/wiki/Ammonia_solution

    Ammonia solution, also known as ammonia water, ammonium hydroxide, ammoniacal liquor, ammonia liquor, aqua ammonia, aqueous ammonia, or (inaccurately) ammonia, is a solution of ammonia in water. It can be denoted by the symbols NH 3 (aq). Although the name ammonium hydroxide suggests a salt with the composition [NH + 4][OH −

  4. Water-reactive substances - Wikipedia

    en.wikipedia.org/wiki/Water-reactive_substances

    Magnesium has a mild reaction with cold water. The reaction is short-lived because the magnesium hydroxide layer formed on the magnesium is almost insoluble in water and prevents further reaction. Mg(s) + 2H 2 O(l) Mg(OH) 2 (s) + H 2 (g) [11] A metal reacting with cold water will produce a metal hydroxide and hydrogen gas.

  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. Schmidt reaction - Wikipedia

    en.wikipedia.org/wiki/Schmidt_reaction

    The protonated isocyanate is attacked by water forming carbamate 4, which after deprotonation loses carbon dioxide to the amine. 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 ...

  7. Wolff rearrangement - Wikipedia

    en.wikipedia.org/wiki/Wolff_rearrangement

    However, trapping with water, to form the acid is the most common form. General homologation reaction, Arndt-Eistert has R 2 = H, RXH=H 2 O. In the most basic form, where R 2 = H, RXH=H 2 O, the reaction lengthens the alkyl chain of a carboxylic acid by a methylene. However, there is great synthetic utility in the variety of reactions one can ...

  8. Dehydration reaction - Wikipedia

    en.wikipedia.org/wiki/Dehydration_reaction

    The classic example of a dehydration reaction is the Fischer esterification, which involves treating a carboxylic acid with an alcohol to give an ester RCO 2 H + R′OH ⇌ RCO 2 R′ + H 2 O. Often such reactions require the presence of a dehydrating agent, i.e. a substance that reacts with water.

  9. Magnesium compounds - Wikipedia

    en.wikipedia.org/wiki/Magnesium_compounds

    Magnesium perchlorate is a white powder that is easily soluble in water, which can be obtained by the reaction of magnesium oxide and perchloric acid. The hexahydrate crystallizes from the solution, and then it is dried with phosphorus pentoxide in a vacuum at 200~250 °C to obtain the anhydrous form.