Definition: This is the point where exactly half of the volume of titrant required to reach the equivalence point has been added. At this stage, the concentration of the weak species equals the concentration of its conjugate ().
Mathematical Significance: According to the Henderson-Hasselbalch equation, . Since the ratio is 1, the log term becomes zero, meaning at this point.
Application: This point is the most accurate way to experimentally determine the acid dissociation constant () of a weak acid or the of a weak base from a titration curve.
Multiple Inflections: Polyprotic acids (like ) have multiple ionizable hydrogens, each with its own value. This results in a titration curve with multiple 'steps' or vertical sections.
Equivalence Points: Each vertical section represents the completion of one neutralization stage. For a diprotic acid, the first equivalence point represents the conversion of to , and the second represents to .
Buffer Regions: Between each equivalence point lies a buffer region where the pH is relatively stable, centered around the of that specific ionization step.
Identify the Analyte: Always look at the starting pH. If it is below 7, the analyte is an acid; if above 7, it is a base. A starting pH of 1 suggests a strong acid, while a pH of 3-5 suggests a weak acid.
Locate the Equivalence Point: Find the center of the steepest vertical climb. The volume at this point is used for stoichiometric calculations ( only applies for 1:1 ratios).
Check the Salt Hydrolysis: If asked why the pH at equivalence isn't 7, explain that the conjugate of the weak reactant reacts with water (hydrolysis) to produce or .
Indicator Selection: An indicator is only valid if its color-change range () falls entirely within the vertical section of the titration curve.