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  2. Inorganic nonaqueous solvent - Wikipedia

    en.wikipedia.org/wiki/Inorganic_nonaqueous_solvent

    The limiting acid in a given solvent is the solvonium ion, such as H 3 O + ion in water.An acid which has more of a tendency to donate a hydrogen ion than the limiting acid will be a strong acid in the solvent considered, and will exist mostly or entirely in its dissociated form.

  3. Gutmann–Beckett method - Wikipedia

    en.wikipedia.org/wiki/Gutmann–Beckett_method

    Gutmann, a chemist renowned for his work on non-aqueous solvents, described an acceptor-number scale for solvent Lewis acidity [4] with two reference points relating to the 31 P NMR chemical shift of Et 3 PO in the weakly Lewis acidic solvent hexane (δ = 41.0 ppm, AN 0) and in the strongly Lewis acidic solvent SbCl 5 (δ = 86.1 ppm, AN 100).

  4. Thermometric titration - Wikipedia

    en.wikipedia.org/wiki/Thermometric_titration

    The procedure can also be used to assist in the analysis of complex acid mixtures containing sulfuric acid where resorting to titration in non-aqueous media is not feasible. The reaction enthalpy for the formation of barium sulfate is a modest −18.8 kJ/mol. This can place a restriction on the lower limit of sulfate in a sample which can be ...

  5. Titration - Wikipedia

    en.wikipedia.org/wiki/Titration

    Back titration is a titration done in reverse; instead of titrating the original sample, a known excess of standard reagent is added to the solution, and the excess is titrated. A back titration is useful if the endpoint of the reverse titration is easier to identify than the endpoint of the normal titration, as with precipitation reactions

  6. Partition coefficient - Wikipedia

    en.wikipedia.org/wiki/Partition_coefficient

    The distribution coefficient, log D, is the ratio of the sum of the concentrations of all forms of the compound (ionized plus un-ionized) in each of the two phases, one essentially always aqueous; as such, it depends on the pH of the aqueous phase, and log D = log P for non-ionizable compounds at any pH.

  7. Determination of equilibrium constants - Wikipedia

    en.wikipedia.org/wiki/Determination_of...

    The analytical (total) concentration of a reactant R at the i th titration point is given by = + [] + where R 0 is the initial amount of R in the titration vessel, v 0 is the initial volume, [R] is the concentration of R in the burette and v i is the volume added. The burette concentration of a reactant not present in the burette is taken to be ...

  8. Acid–base titration - Wikipedia

    en.wikipedia.org/wiki/Acid–base_titration

    The history of acid-base titration dates back to the late 19th century when advancements in analytical chemistry fostered the development of systematic techniques for quantitative analysis. [5] The origins of titration methods can be linked to the work of chemists such as Karl Friedrich Mohr in the mid-1800s. [5]

  9. Standard solution - Wikipedia

    en.wikipedia.org/wiki/Standard_solution

    In titrations, the concentration of analyte in solution can be determined by titrating the standard solution against the analyte solution to determine the threshold of neutralization. [9] For example, to calculate the concentration of hydrogen chloride, a standard solution of known concentration, such as 0.5 M sodium hydroxide, is titrated ...