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  2. Boron trifluoride - Wikipedia

    en.wikipedia.org/wiki/Boron_trifluoride

    The reaction commences with the formation of the aquo adduct, H 2 O−BF 3, which then loses HF that gives fluoroboric acid with boron trifluoride. [22] 4 BF 3 + 3 H 2 O → 3 H[BF 4] + B(OH) 3. The heavier trihalides do not undergo analogous reactions, possibly due to the lower stability of the tetrahedral ions [BCl 4] − and [BBr 4] −.

  3. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    A Lewis base is often a Brønsted–Lowry base as it can donate a pair of electrons to H +; [11] the proton is a Lewis acid as it can accept a pair of electrons. The conjugate base of a Brønsted–Lowry acid is also a Lewis base as loss of H + from the acid leaves those electrons which were used for the A—H bond as a lone pair on the ...

  4. Boron trifluoride etherate - Wikipedia

    en.wikipedia.org/wiki/Boron_trifluoride_etherate

    Boron trifluoride etherate, strictly boron trifluoride diethyl etherate, or boron trifluoride–ether complex, is the chemical compound with the formula BF 3 O(C 2 H 5) 2, often abbreviated BF 3 OEt 2.

  5. Fluoroboric acid - Wikipedia

    en.wikipedia.org/wiki/Fluoroboric_acid

    Pure H[BF 4] has not been described. The same holds true for the superacids that are known by the simplified formulas H[PF 6] and H[SbF 6]. [4] [5] However, a solution of BF 3 in HF is highly acidic, having an approximate speciation of [H 2 F] + [BF 4] − (fluoronium tetrafluoroborate) and a Hammett acidity function of −16.6 at 7 mol % BF 3, easily qualifying as a superacid. [6]

  6. Lewis acid catalysis - Wikipedia

    en.wikipedia.org/wiki/Lewis_Acid_Catalysis

    Two common modes of Lewis acid catalysis in reactions with polar mechanisms. In reactions with polar mechanisms, Lewis acid catalysis often involves binding of the catalyst to Lewis basic heteroatoms and withdrawing electron density, which in turn facilitates heterolytic bond cleavage (in the case of Friedel-Crafts reaction) or directly activates the substrate toward nucleophilic attack (in ...

  7. Brønsted–Lowry acid–base theory - Wikipedia

    en.wikipedia.org/wiki/Brønsted–Lowry_acid...

    The essence of Brønsted–Lowry theory is that an acid is only such in relation to a base, and vice versa. Water is amphoteric as it can act as an acid or as a base. In the image shown at the right one molecule of H 2 O acts as a base and gains H + to become H 3 O + while the other acts as an acid and loses H + to become OH −.

  8. Talk:Boron trifluoride - Wikipedia

    en.wikipedia.org/wiki/Talk:Boron_trifluoride

    There is no lone pair on boron, whereas nitrogen in ammonia has a lone pair, which repels the three N-H bonds, resulting in a pyramidal molecule. Ben 16:12, 3 May 2008 (UTC) Thank you on your clarification! In this case, why is the article page showing BF 3 having pyramidal structure? Juraj5 18:30, 5 May 2008 (UTC) It doesn't.

  9. Acid–base reaction - Wikipedia

    en.wikipedia.org/wiki/Acid–base_reaction

    In chemistry, an acid–base reaction is a chemical reaction that occurs between an acid and a base.It can be used to determine pH via titration.Several theoretical frameworks provide alternative conceptions of the reaction mechanisms and their application in solving related problems; these are called the acid–base theories, for example, Brønsted–Lowry acid–base theory.