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  2. Smelling salts - Wikipedia

    en.wikipedia.org/wiki/Smelling_salts

    In the 17th century, the distillation of an ammonia solution from shavings of harts' (deer) horns and hooves led to the alternative name for smelling salts as spirit or salt of hartshorn. [ 1 ] They were widely used in Victorian Britain to revive fainting women, and in some areas, constables would carry a container of them for that purpose. [ 10 ]

  3. Tincture - Wikipedia

    en.wikipedia.org/wiki/Tincture

    Spirit of ammonia (spirits of hartshorn) Spirit of camphor; Spirit of ether, a solution of diethyl ether in alcohol "Spirit of Mindererus", ammonium acetate in alcohol "Spirit of nitre" is not a spirit in this sense, but an old name for nitric acid (but "sweet spirit of nitre" was ethyl nitrite) Similarly "spirit(s) of salt" actually meant ...

  4. Aromatization - Wikipedia

    en.wikipedia.org/wiki/Aromatization

    Aromatization is a chemical reaction in which an aromatic system is formed from a single nonaromatic precursor. Typically aromatization is achieved by dehydrogenation of existing cyclic compounds, illustrated by the conversion of cyclohexane into benzene. Aromatization includes the formation of heterocyclic systems.

  5. 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).

  6. Aromatic compound - Wikipedia

    en.wikipedia.org/wiki/Aromatic_compound

    Heteroarenes are aromatic compounds, where at least one methine or vinylene (-C= or -CH=CH-) group is replaced by a heteroatom: oxygen, nitrogen, or sulfur. [3] Examples of non-benzene compounds with aromatic properties are furan, a heterocyclic compound with a five-membered ring that includes a single oxygen atom, and pyridine, a heterocyclic compound with a six-membered ring containing one ...

  7. Ammonolysis - Wikipedia

    en.wikipedia.org/wiki/Ammonolysis

    Ammonolysis can be used to synthesize nitrides (and oxynitrides) by reacting various metal precursors with ammonia, some options include chemical vapor deposition, [3] treating metals or metal oxides with ammonia gas, [15] or liquid supercritical ammonia (also known as "ammonothermal" synthesis, analogous to hydrothermal synthesis).

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  9. Hantzsch pyridine synthesis - Wikipedia

    en.wikipedia.org/wiki/Hantzsch_pyridine_synthesis

    The Hantzsch pyridine synthesis or Hantzsch dihydropyridine synthesis is a multi-component organic reaction between an aldehyde such as formaldehyde, 2 equivalents of a β-keto ester such as ethyl acetoacetate and a nitrogen donor such as ammonium acetate or ammonia.