The pKa of an acid can be determined through (reduction, titration, filtration) with a strong base. Gradually increase the volume of the base, stopping (before, as, after) the equivalence point is reached.
The pKa of the acid is equal to the pH at the (equivalence point, midway volume to the equivalence point, maximum volume).

The pKa of an acid can be determined through titration with a strong base.

Gradually increase the volume of the base, stopping before the equivalence point is reached.

The pKa of the acid is equal to the pH at the midway volume to the equivalence point.

Explanation:

An acid HA dissociates in water as follows:

HA ⇄ H⁺ + A⁻      Ka

So, it produces hydrogen ions (H⁺) and a conjugate base (A⁻). The concentrations of HA, H⁺ and A⁻ at equilibrium determine the constant Ka. The pKa is calculated as:

pKa = -log Ka

The relationship between the pH of the solution and the pKa of the acid is described by the Henderson-Hasselbalch equation:

pH = pKa + log ([A⁻]/[HA])

The pKa can be experimentally determined by acid-base titration, in which a strong base is added to the acid solution. As the base is added, the acid HA is neutralized and the conjugate base A⁻ is formed. Thus, the concentration of the acid ([HA]) increases and the concentration of the conjugate base ([A⁻] decreases. The equivalence point is reached when the total amount of acid is neutralized with the added base. Before reaching the equivalence point, at the halfway point, half of the acid is neutralized and converted into the conjugate base. Thus:

[A-] = [HA] ⇒ log [A-]/[HA] = log 1 = 0 ⇒ pH = pKa

We measure the pH at that point and it is equal to the pKa of the acid.

2b2t

explanation:

2b2t