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In solution chemistry, it is common to use H + as an abbreviation for the solvated hydrogen ion, regardless of the solvent. In aqueous solution H + denotes a solvated hydronium ion rather than a proton. [9] [10] The designation of an acid or base as "conjugate" depends on the context. The conjugate acid BH + of a base B dissociates according to
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.
For reactions in aqueous solution, such as an acid dissociation reaction AH + H 2 O ⇌ A − + H 3 O + the concentration of water may be taken as being constant and the formation of the hydronium ion is implicit. AH ⇌ A − + H + Water concentration is omitted from expressions defining equilibrium constants, except when solutions are very ...
The reaction usually requires a catalyst, such as concentrated sulfuric acid: R−OH + R'−CO 2 H → R'−CO 2 R + H 2 O. Other types of ester are prepared in a similar manner−for example, tosyl (tosylate) esters are made by reaction of the alcohol with 4-toluenesulfonyl chloride in pyridine.
For a strong acid-strong base titration monitored by pH, we have at any i'th point in the titration = [+] [] where K w is the water autoprotolysis constant.. If titrating an acid of initial volume and concentration [+] with base of concentration [], then at any i'th point in the titration with titrant volume ,
For both (a) and (b), i) describes the catalytic cycle with relevant rate constants and concentrations, ii) displays the concentration of product and reactant over the course of the reaction, iii) describes the rate of the reaction as substrate is consumed from right to left, and iv) shows that the catalyst resting state is an equilibrium ...
In strongly basic solutions, phenolphthalein is converted to its In(OH) 3− form, and its pink color undergoes a rather slow fading reaction [6] and becomes completely colorless when pH is greater than 13. The pK a values of phenolphthalein were found to be 9.05, 9.50 and 12 while those of phenolsulfonphthalein are 1.2 and 7.70.