1.0 g KOH is added to the buffer. First change the mass to moles: 1.0 g KOH × 1 mol KOH/(39.1 g + 16.0 g + 1.0 g) = 0.018 mol in 1.00 L
[KOH] = 0.018 M
(The pH of this strong base in the absence of buffer would be pOH = –log(0.018) = 1.74 so pH = 14.00 – 1.74 = 12.26)
NaNO2(aq) → Na+(aq) + NO2–(aq)
HNO2(aq) + H2O(l) → ← H3O+(aq) + NO2–(aq)
A/B reaction:HNO2(aq) + KOH(aq) → K+(aq) + NO2–(aq) + H2O(l)
Ka = [H3O+]e[NO2–]e [HNO2]e = 7.2×10–4
Initial0.150 0 0.200
A/B reaction–0.018 0 +0.018
Change– x +x +x
Equilibrium0.132 – x x 0.218 + x
Approximate? 0.132/7.2×10–4 = 180 > 100 Yes.
7.2×10–4 = (x)(0.218)/(0.132)
x = [H3O+]e = 4.4×10–4 M
pH = –log[H3O+] = –log(4.4×10–4) = 3.36