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  2. Acid dissociation constant - Wikipedia

    en.wikipedia.org/wiki/Acid_dissociation_constant

    [c] [2] For example, a hypothetical weak acid having K a = 10 −5, the value of log K a is the exponent (−5), giving pK a = 5. For acetic acid, K a = 1.8 x 10 −5, so pK a is 4.7. A higher K a corresponds to a stronger acid (an acid that is more dissociated at equilibrium).

  3. Buffer solution - Wikipedia

    en.wikipedia.org/wiki/Buffer_solution

    Buffer capacity falls to 33% of the maximum value at pH = pK a ± 1, to 10% at pH = pK a ± 1.5 and to 1% at pH = pK a ± 2. For this reason the most useful range is approximately pK a ± 1. When choosing a buffer for use at a specific pH, it should have a pK a value as close as possible to that pH. [2]

  4. Acid strength - Wikipedia

    en.wikipedia.org/wiki/Acid_strength

    Such a statement is incorrect. For example, acetic acid is a weak acid which has a = 1.75 x 10 −5. Its conjugate base is the acetate ion with K b = 10 −14 /K a = 5.7 x 10 −10 (from the relationship K a × K b = 10 −14), which certainly does not correspond to a strong base

  5. Dissociation constant - Wikipedia

    en.wikipedia.org/wiki/Dissociation_constant

    For example, if a macromolecule M has three binding sites, K′ 1 describes a ligand being bound to any of the three binding sites. In this example, K′ 2 describes two molecules being bound and K′ 3 three molecules being bound to the macromolecule. The microscopic or individual dissociation constant describes the equilibrium of ligands ...

  6. Henderson–Hasselbalch equation - Wikipedia

    en.wikipedia.org/wiki/Henderson–Hasselbalch...

    For example, the acid may be acetic acid and the salt may be sodium acetate. The Henderson–Hasselbalch equation relates the pH of a solution containing a mixture of the two components to the acid dissociation constant , K a of the acid, and the concentrations of the species in solution.

  7. Protein pKa calculations - Wikipedia

    en.wikipedia.org/wiki/Protein_pKa_calculations

    The pK a 12 is equal to the Henderson–Hasselbalch pK a (pK HH a ) if the titration curve follows the Henderson–Hasselbalch equation . [ 14 ] Most p K a calculation methods silently assume that all titration curves are Henderson–Hasselbalch shaped, and p K a values in p K a calculation programs are therefore often determined in this way.

  8. Pyrazole - Wikipedia

    en.wikipedia.org/wiki/Pyrazole

    Pyrazole is a weak base, with pK b 11.5 (pK a of the conjugate acid 2.49 at 25 °C). [3] According to X-ray crystallography , the compound is planar. The two C-N distances are similar, both near 1.33 Å [ 4 ]

  9. pH - Wikipedia

    en.wikipedia.org/wiki/PH

    The measurement of pH can become difficult at extremely acidic or alkaline conditions, such as below pH 2.5 (ca. 0.003 mol/dm 3 acid) or above pH 10.5 (above ca. 0.0003 mol/dm 3 alkaline). This is due to the breakdown of the Nernst equation in such conditions when using a glass electrode.