Ammonolysis
Any chemical reaction with ammonia as a reactant
In chemistry, ammonolysis (/am·mo·nol·y·sis/) is the process of splitting ammonia into NH 2 − + H + {\displaystyle {\ce {NH2- + H+}}} . Ammonolysis reactions can be conducted with organic compounds to produce amines (molecules containing a nitrogen atom with a lone pair, :N), or with inorganic compounds to produce nitrides.
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Ammonolysis
Any chemical reaction with ammonia as a reactant
In chemistry, ammonolysis (/am·mo·nol·y·sis/) is the process of splitting ammonia into NH 2 − + H + {\displaystyle {\ce {NH2- + H+}}} . Ammonolysis reactions can be conducted with organic compounds to produce amines (molecules containing a nitrogen atom with a lone pair, :N), or with inorganic compounds to produce nitrides.
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In chemistry, ammonolysis (/am·mo·nol·y·sis/) is the process of splitting ammonia into NH 2 − + H + {\displaystyle {\ce {NH2- + H+}}} . Ammonolysis reactions can be conducted with organic compounds to produce amines (molecules containing a nitrogen atom with a lone pair, :N), or with inorganic compounds to produce nitrides. This reaction is analogous to hydrolysis in which water molecules are split. Similar to water, liquid ammonia also undergoes auto-ionization, 2 NH 3 ⇌ NH 4 + + NH 2 − {\displaystyle {\ce {{2 NH3 ⇌ NH4+ + NH2- }}}} , where the rate constant is k = 1.9 × 10−38. Organic compounds such as alkyl halides, hydroxyls (hydroxyl nitriles and carbohydrates), carbonyl (aldehydes/ketones/esters/alcohols), and sulfur (sulfonyl derivatives) can all undergo ammonolysis in liquid ammonia.
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