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  2. Acidity function - Wikipedia

    en.wikipedia.org/wiki/Acidity_function

    An acidity function is a measure of the acidity of a medium or solvent system, [1] [2] usually expressed in terms of its ability to donate protons to (or accept protons from) a solute (Brønsted acidity). The pH scale is by far the most commonly used acidity function, and is ideal for dilute aqueous solutions.

  3. pH - Wikipedia

    en.wikipedia.org/wiki/PH

    A strong acid, such as hydrochloric acid, at concentration 1 mol dm −3 has a pH of 0, while a strong alkali like sodium hydroxide, at the same concentration, has a pH of 14. Since pH is a logarithmic scale, a difference of one in pH is equivalent to a tenfold difference in hydrogen ion concentration.

  4. Acid dissociation constant - Wikipedia

    en.wikipedia.org/wiki/Acid_dissociation_constant

    Nitric acid, with a pK value of around −1.7, behaves as a strong acid in aqueous solutions with a pH greater than 1. [23] At lower pH values it behaves as a weak acid. pK a values for strong acids have been estimated by theoretical means. [24] For example, the pK a value of aqueous HCl has been estimated as −9.3.

  5. Phenyl group - Wikipedia

    en.wikipedia.org/wiki/Phenyl_group

    In organic chemistry, the phenyl group, or phenyl ring, is a cyclic group of atoms with the formula C6H5, and is often represented by the symbol Ph (archaically φ) or Ø. The phenyl group is closely related to benzene and can be viewed as a benzene ring, minus a hydrogen, which may be replaced by some other element or compound to serve as a ...

  6. Acid catalysis - Wikipedia

    en.wikipedia.org/wiki/Acid_catalysis

    In specific acid catalysis, protonated solvent is the catalyst. The reaction rate is proportional to the concentration of the protonated solvent molecules SH +. [6] The acid catalyst itself (AH) only contributes to the rate acceleration by shifting the chemical equilibrium between solvent S and AH in favor of the SH + species. This kind of ...

  7. Solvent effects - Wikipedia

    en.wikipedia.org/wiki/Solvent_effects

    The determining factor when both S N 2 and S N 1 reaction mechanisms are viable is the strength of the Nucleophile. Nuclephilicity and basicity are linked and the more nucleophilic a molecule becomes the greater said nucleophile's basicity. This increase in basicity causes problems for S N 2 reaction mechanisms when the solvent of choice is protic.

  8. Alkalinity - Wikipedia

    en.wikipedia.org/wiki/Alkalinity

    Alkalinity can be measured by titrating a sample with a strong acid until all the buffering capacity of the aforementioned ions above the pH of bicarbonate or carbonate is consumed. This point is functionally set to pH 4.5. At this point, all the bases of interest have been protonated to the zero level species, hence they no longer cause ...

  9. Chemical property - Wikipedia

    en.wikipedia.org/wiki/Chemical_property

    A chemical property is any of a material's properties that becomes evident during, or after, a chemical reaction; that is, any attribute that can be established only by changing a substance's chemical identity. [1] Simply speaking, chemical properties cannot be determined just by viewing or touching the substance; the substance's internal ...