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  2. Ammonia - Wikipedia

    en.wikipedia.org/wiki/Ammonia

    Ammonia is an inorganic chemical compound of nitrogen and hydrogen with the formula N H 3.A stable binary hydride and the simplest pnictogen hydride, ammonia is a colourless gas with a distinctive pungent smell.

  3. Ammonia (data page) - Wikipedia

    en.wikipedia.org/wiki/Ammonia_(data_page)

    Table data (above) obtained from CRC Handbook of Chemistry and Physics 44th ed. The (s) notation indicates equilibrium temperature of vapor over solid. Otherwise temperature is equilibrium of vapor over liquid.

  4. Ammonia solution - Wikipedia

    en.wikipedia.org/wiki/Ammonia_solution

    In aqueous solution, ammonia deprotonates a small fraction of the water to give ammonium and hydroxide according to the following equilibrium: . NH 3 + H 2 O ⇌ NH + 4 + OH −.. In a 1 M ammonia solution, about 0.42% of the ammonia is converted to ammonium, equivalent to pH = 11.63 because [NH +

  5. Acid dissociation constant - Wikipedia

    en.wikipedia.org/wiki/Acid_dissociation_constant

    In chemistry, an acid dissociation constant (also known as acidity constant, or acid-ionization constant; denoted ⁠ ⁠) is a quantitative measure of the strength of an acid in solution.

  6. Amine - Wikipedia

    en.wikipedia.org/wiki/Amine

    Amine. In chemistry, amines (/ ə ˈ m iː n, ˈ æ m iː n /, [1] [2] UK also / ˈ eɪ m iː n / [3]) are compounds and functional groups that contain a basic nitrogen atom with a lone pair.Formally, amines are derivatives of ammonia (NH 3 (in which the bond angle between the nitrogen and hydrogen is 107°), wherein one or more hydrogen atoms have been replaced by a substituent such as an ...

  7. Ammonium bicarbonate - Wikipedia

    en.wikipedia.org/wiki/Ammonium_bicarbonate

    Ammonium bicarbonate is produced by combining carbon dioxide and ammonia: CO 2 + NH 3 + H 2 O → (NH 4)HCO 3. Since ammonium bicarbonate is thermally unstable, the reaction solution is kept cold, which allows the precipitation of the product as white solid.

  8. Non-nucleophilic base - Wikipedia

    en.wikipedia.org/wiki/Non-nucleophilic_base

    As the name suggests, a non-nucleophilic base is a sterically hindered organic base that is a poor nucleophile.Normal bases are also nucleophiles, but often chemists seek the proton-removing ability of a base without any other functions.

  9. Carbamic acid - Wikipedia

    en.wikipedia.org/wiki/Carbamic_acid

    Carbamic acid is a planar molecule. [3]The H 2 N− group of carbamic acid, unlike that of most amines, cannot be protonated to an ammonium group H 3 N + −.The zwitterionic form H 3 N + −COO − is very unstable and promptly decomposes into ammonia and carbon dioxide, [6] yet there is a report of its detection in ices irradiated with high-energy protons.