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  2. Dissociation (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Dissociation_(chemistry)

    A weak electrolyte is a substance whose solute exists in solution mostly in the form of molecules (which are said to be "undissociated"), with only a small fraction in the form of ions. Simply because a substance does not readily dissolve does not make it a weak electrolyte. Acetic acid (CH 3 COOH) and ammonium (NH + 4) are good examples ...

  3. Glucuronic acid - Wikipedia

    en.wikipedia.org/wiki/Glucuronic_acid

    Depending on the configuration at C-1, there are two anomers of glucuronic acid, α- and β-form. In β-D-glucuronic acid the C-1 hydroxy group is on the same side of the pyranose ring as the carboxyl group. In the free sugar acid, the β-form is prevalent (~64%), whereas in the organism, the α-form UDP-α-D-glucuronic acid (UDPGA) predominates.

  4. Acid strength - Wikipedia

    en.wikipedia.org/wiki/Acid_strength

    For instance, hydrogen fluoride, whether dissolved in water (= 3.2) or DMSO (= 15), has values indicating that it undergoes incomplete dissociation in these solvents, making it a weak acid. However, as the rigorously dried, neat acidic medium, hydrogen fluoride has an H 0 {\displaystyle H_{0}} value of –15, [ 1 ] making it a more strongly ...

  5. Acid dissociation constant - Wikipedia

    en.wikipedia.org/wiki/Acid_dissociation_constant

    In water, measurable pK a values range from about −2 for a strong acid to about 12 for a very weak acid (or strong base). A buffer solution of a desired pH can be prepared as a mixture of a weak acid and its conjugate base. In practice, the mixture can be created by dissolving the acid in water, and adding the requisite amount of strong acid ...

  6. Sugar acid - Wikipedia

    en.wikipedia.org/wiki/Sugar_acid

    Main classes of sugar acids include: Aldonic acids , in which the aldehyde group ( −CH=O ) located at the initial end ( position 1 ) of an aldose is oxidized. Ulosonic acids , in which the hydroxymethyl group ( −CH 2 OH ) at the initial end of a 2- ketose is oxidized creating an α- ketoacid .

  7. Enthalpy change of solution - Wikipedia

    en.wikipedia.org/wiki/Enthalpy_change_of_solution

    The equilibrium, between the gas as a separate phase and the gas in solution, will by Le Châtelier's principle shift to favour the gas going into solution as the temperature is decreased (decreasing the temperature increases the solubility of a gas). When a saturated solution of a gas is heated, gas comes out of the solution.

  8. Aqueous solution - Wikipedia

    en.wikipedia.org/wiki/Aqueous_solution

    This reaction occurs when two aqueous strong electrolyte solutions mix and produce an insoluble solid, also known as a precipitate. The ability of a substance to dissolve in water is determined by whether the substance can match or exceed the strong attractive forces that water molecules generate

  9. Sucrose - Wikipedia

    en.wikipedia.org/wiki/Sucrose

    The sugar-refining process involves washing the raw sugar crystals before dissolving them into a sugar syrup which is filtered and then passed over carbon to remove any residual colour. The sugar syrup is then concentrated by boiling under a vacuum and crystallized as the final purification process to produce crystals of pure sucrose that are ...