In: Chemistry
for the pKa value first let us find percent ionisation to molarity
As 100% gives 0.08M concentration of H+ or pH of solution is -log(0.08) =1.096
2.3% ionisation = 2.3*0.08/100=1.84*10-3M concentration of H+
Ka = [A-]eq [H+]eq/[HA]eq
We know the equilibrium concentration of H+, since we were given the pH of the solution. [H+]eq = 1.84*10-3M
2. We know the initial concentration of HA. We will lose x moles of this as the acid undergoes dissociation to form A- and H+.
3. [HA](M) [H+](M) [A-](M)
Initial 0.08 0.00 0.00
Change -x +x +x
Equilibrium 0.08 -x x x
Ka = (x)(x)
(0.08 - x)
4. Assume that all of the H+ comes from the acid, and none from water. We know that the [H+]eq = 1.84*10-3M
We can also see that the concentration of HA will change very little, from 0.08 to 0.08 - 1.84 x 10-3. The change in concentration can be ignored if it is less than 5% of the original concentration. 0.08 M x 5%, so the change in [HA] in this problem can be ignored.
Ka=(1.84*10-3)2/0.08=4.2*10-5
Ka = 10^(-pKa)
so pKa=4.37