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  2. Markovnikov's rule - Wikipedia

    en.wikipedia.org/wiki/Markovnikov's_rule

    Markovnikov's rule is illustrated by the reaction of propene with hydrobromic acid. In organic chemistry, Markovnikov's rule or Markownikoff's rule describes the outcome of some addition reactions. The rule was formulated by Russian chemist Vladimir Markovnikov in 1870. [1] [2] [3]

  3. Inorganic nonaqueous solvent - Wikipedia

    en.wikipedia.org/wiki/Inorganic_nonaqueous_solvent

    For example, the limiting acid in liquid ammonia is the ammonium ion, NH 4 + which has a pK a value in water of 9.25. The limiting base is the amide ion, NH 2-. NH 2 − is a stronger base than the hydroxide ion and so cannot exist in aqueous solution. The pK a value of ammonia is estimated to be approximately 34 (c.f. water, 14 [3] [4]).

  4. Talk:Titration - Wikipedia

    en.wikipedia.org/wiki/Talk:Titration

    The sigmoid curve for a multiprotic acid should show apparent "steps," but citric acid often fails to do that. 129.93.105.60 10:39, 30 January 2006 (UTC) Thought I'd add a comment [ reply ] History of volumetric analysis

  5. List of saturated fatty acids - Wikipedia

    en.wikipedia.org/wiki/List_of_saturated_fatty_acids

    Pentanoic acid CH 3 (CH 2) 3 COOH C5:0 Caproic acid: Hexanoic acid CH 3 (CH 2) 4 COOH C6:0 Enanthic acid: Heptanoic acid CH 3 (CH 2) 5 COOH C7:0 Caprylic acid: Octanoic acid CH 3 (CH 2) 6 COOH C8:0 Pelargonic acid: Nonanoic acid CH 3 (CH 2) 7 COOH C9:0 Capric acid: Decanoic acid CH 3 (CH 2) 8 COOH C10:0 Undecylic acid: Undecanoic acid CH 3 (CH ...

  6. Amphoterism - Wikipedia

    en.wikipedia.org/wiki/Amphoterism

    Other examples of inorganic polyprotic acids include anions of sulfuric acid, phosphoric acid and hydrogen sulfide that have lost one or more protons. In organic chemistry and biochemistry, important examples include amino acids and derivatives of citric acid. Although an amphiprotic species must be amphoteric, the converse is not true.

  7. Valproate - Wikipedia

    en.wikipedia.org/wiki/Valproate

    Valproic acid was first synthesized in 1882 by Beverly S. Burton as an analogue of valeric acid, found naturally in valerian. [69] Valproic acid is a carboxylic acid, a clear liquid at room temperature. For many decades, its only use was in laboratories as a "metabolically inert" solvent for organic compounds.

  8. Protic ionic liquid - Wikipedia

    en.wikipedia.org/wiki/Protic_ionic_liquid

    A protic ionic liquid is an ionic liquid that is formed via proton transfer from a Brønsted acid to a Brønsted base. [1] Unlike many other types of ionic liquids, which are formed through a series of synthesis steps, [2] protic ionic liquids are easier to create because the acid and base must simply be mixed together. [1]

  9. Protic acid - Wikipedia

    en.wikipedia.org/?title=Protic_acid&redirect=no

    This page was last edited on 24 October 2008, at 07:35 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  1. Related searches multiprotic acid

    titration of multiprotic acidpolyprotic acid