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Express each concentration value as the ratio c/c 0, where c 0 is the concentration in a [hypothetical] standard state, with a numerical value of 1, by definition. [19] Express the concentrations on the mole fraction scale. Since mole fraction has no dimension, the quotient of concentrations will, by definition, be a pure number.
depending on whether the electrode is calibrated in millivolts or pH. For convenience the concentration, [H +], is used in place of activity. In a titration of strong acid with strong alkali, the analytical concentration of the hydrogen ion is obtained from the initial concentration of acid, C i and the amount of alkali added during titration.
In chemistry, an alcohol (from Arabic al-kuḥl 'the kohl'), [2] is a type of organic compound that carries at least one hydroxyl (−OH) functional group bound to a saturated carbon atom. [ 3 ] [ 4 ] Alcohols range from the simple, like methanol and ethanol , to complex, like sugar alcohols and cholesterol .
C A is the analytical concentration of the acid and C H is the concentration the hydrogen ion that has been added to the solution. The self-dissociation of water is ignored. A quantity in square brackets, [X], represents the concentration of the chemical substance X. It is understood that the symbol H + stands for the hydrated hydronium ion.
When the acidic medium in question is a dilute aqueous solution, the is approximately equal to the pH value, which is a negative logarithm of the concentration of aqueous + in solution. The pH of a simple solution of an acid in water is determined by both K a {\displaystyle K_{{\ce {a}}}} and the acid concentration.
Phase behavior Triple point: 150 K (−123 °C), 0.00043 Pa Critical point: 514 K (241 °C), 63 bar Std enthalpy change of fusion, Δ fus H o +4.9 kJ/mol
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 ...
FDPB-based methods calculate the change in the pK a value of an amino acid side chain when that side chain is moved from a hypothetical fully solvated state to its position in the protein. To perform such a calculation, one needs theoretical methods that can calculate the effect of the protein interior on a p K a value, and knowledge of the pKa ...