A2 · Practice questions · The Nernst equation

Put the concentrations in.

Six original Cambridge-style questions on the Nernst equation and non-standard cells.

Original questions All questions on this page are original work, written in the Cambridge AS & A Level style. They are not from past papers. They test the same concepts and skills the syllabus rewards.
Keep these straight

Oxidised on top, divide by z, base-10 log.

01
Calculation
[2 marks]

Calculate the electrode potential of a Ag+/Ag half-cell in which [Ag+] = 0.050 mol dm−3. (E⊖ = +0.80 V)

  • z = 1: E = 0.80 + 0.059 log 0.050. ✓
  • E = 0.80 + 0.059 × (−1.301) = +0.723 V. ✓
02
Calculation
[3 marks]

Calculate Ecell for the cell Zn | Zn2+ (0.50 mol dm−3) || Ag+ (0.20 mol dm−3) | Ag.

  • E(Ag) = 0.80 + 0.059 log 0.20 = 0.80 − 0.0412 = +0.759 V. ✓
  • E(Zn) = −0.76 + 0.0295 log 0.50 = −0.76 − 0.0089 = −0.769 V. ✓
  • Ecell = 0.759 − (−0.769) = +1.53 V. ✓
03
Calculation
[2 marks]

Calculate E for the Fe3+/Fe2+ half-cell when [Fe3+] = 0.10 mol dm−3 and [Fe2+] = 1.0 mol dm−3. Would Fe3+ still oxidise I− under standard conditions for the iodine half-cell?

  • E = 0.77 + 0.059 log (0.10 ÷ 1.0) = +0.711 V. ✓
  • Ecell = 0.711 − 0.54 = +0.171 V, still positive, so yes. ✓
04
Explain
[3 marks]

Explain, in terms of the equilibrium Cl2 + 2e− ⇌ 2Cl−, why chlorine rather than oxygen is the main anode product when concentrated sodium chloride solution is electrolysed.

  • A high [Cl−] shifts the equilibrium to the left (reduced form increased). ✓
  • So E(Cl2/Cl−) becomes less positive than +1.36 V, approaching or below E(O2/H2O). ✓
  • Cl− is therefore oxidised in preference to water, giving chlorine. ✓
05
Calculation
[2 marks]

Calculate E for the Cl2/Cl− half-cell when [Cl−] = 2.0 mol dm−3 and chlorine is at 100 kPa. (E⊖ = +1.36 V)

  • E = 1.36 + (0.059 ÷ 2) log (1 ÷ 2.02) = 1.36 − 0.059 log 2.0. ✓
  • E = 1.36 − 0.0178 = +1.34 V. ✓
06
Analysis
[3 marks]

A cell is set up from two Cu2+/Cu half-cells, one with [Cu2+] = 1.00 mol dm−3 and one with 0.010 mol dm−3. Calculate the e.m.f., identify the positive electrode and state what happens to the e.m.f. as the cell runs.

  • E(dilute) = 0.34 + 0.0295 log 0.010 = +0.281 V; E(concentrated) = +0.340 V. ✓
  • Ecell = 0.340 − 0.281 = 0.059 V; the 1.00 mol dm−3 electrode is positive (Cu2+ is reduced there). ✓
  • As it runs, the concentrated side becomes more dilute and the dilute side more concentrated, so the e.m.f. falls towards zero. ✓

Mark this once you have attempted all six and checked your working. It records a Practiced badge on the topic and adds a one-time bonus. Revealing the solutions alone does not count.