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9701 A Level Chemistry/ Topic 24 Electrochemistry/ 6 interactive simulations/ drag to rotate 3D scenes

Electrode potentials and electrolysis, made interactive

Six simulations covering Topic 24: an electrolysis cell where you choose the electrolyte and watch which ion is discharged at each electrode; Q = It and the Faraday constant turned into a mass of copper or a volume of hydrogen, and the copper experiment that gives the Avogadro constant; the standard hydrogen electrode wired to a second half-cell to measure E°; a cell built from any two half-cells with the electron flow, the positive electrode and the overall equation; a feasibility checker for any oxidising agent against any reducing agent; and the Nernst equation, with E redrawn as the concentrations change.

1. Which ion is discharged? 2D · 24.1

An electrolyte conducts because its ions can move. Pass a direct current through it and the cations drift to the negative electrode (the cathode) where they gain electrons, while the anions drift to the positive electrode (the anode) where they lose them. In a molten salt there is only one choice at each electrode. In solution, water joins in, and which ion is discharged depends on the electrode potentials and on the concentration.

Electrolyte

AT THE CATHODE (−)
AT THE ANODE (+)
IONS PRESENT

2. Q = It and the Faraday constant 2D · 24.1

The amount of product at an electrode depends only on how much charge has passed. Charge is current multiplied by time, one mole of electrons carries one Faraday (96 500 C), and the half-equation tells you how many moles of electrons each mole of product needs. Set the current and time, pick the product, and follow the working. Then run the copper experiment backwards to measure the Avogadro constant.

Product at the electrode

CHARGE Q = It
MOLES OF ELECTRONS
MOLES OF PRODUCT
MASS
F = Le, where L is the Avogadro constant and e the charge on one electron, 1.60 × 10−19 C. In the copper experiment the cathode is weighed before and after, the current is kept steady with a variable resistor and the time is measured. Molar gas volume 24.0 dm3 at room temperature and pressure.

3. The standard hydrogen electrode 3D · 24.2

A single half-cell has no measurable voltage on its own; a voltmeter needs two electrodes. Chemists agreed on a reference: hydrogen gas at 1 atm bubbling over platinum in a solution containing 1.00 mol dm−3 of H+ at 298 K, defined as 0.00 V. The standard electrode potential of any other half-cell is the voltage it gives when connected to this reference under standard conditions.

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Half-cell on the right

VOLTMETER READING
ELECTRODE
ELECTRONS FLOW
HALF-EQUATION (as written in the Data Booklet)
Standard conditions: all solutions 1.00 mol dm−3, gases at 1 atm (101 kPa), 298 K. For an ion/ion system such as Fe3+/Fe2+ both ions are present at 1.00 mol dm−3 and an inert platinum electrode carries the electrons. The salt bridge (filter paper soaked in KNO3) completes the circuit and lets ions move without the solutions mixing.

4. Which way do the electrons go? 2D · 24.2

Connect any two half-cells and the one with the more positive E° becomes the positive electrode: reduction happens there, and it pulls electrons through the wire from the other electrode, where oxidation happens. E°cell = E°(right) − E°(left). If that comes out negative, the electrons are simply flowing the other way; swap the half-cells and the same number appears with a plus sign.

Left half-cell

Right half-cell

E°cell = E°(right) − E°(left)
POSITIVE ELECTRODE
ELECTRONS FLOW
OVERALL EQUATION
Exam point: E°cell is also E°(positive electrode) − E°(negative electrode), which is always a positive number. To get the overall equation, reverse the half-equation with the less positive E° and multiply so the electrons cancel. Multiplying a half-equation never changes its E°.

5. Feasible, but will it happen? 2D · 24.2

Lay the half-equations out on a ladder of E° values. The species on the left of a half-equation high up the ladder are strong oxidising agents; the species on the right of one low down are strong reducing agents. An oxidising agent can oxidise any reducing agent that sits lower on the ladder, because E°cell for that pairing is positive. Pick a pair and test it, then read the caveats.

Oxidising agent (left-hand species, gains electrons)

Reducing agent (right-hand species, loses electrons)

E°cell = E°(oxidising agent) − E°(reducing agent)
VERDICT
EQUATION
A positive E°cell says a reaction is thermodynamically feasible under standard conditions. It says nothing about the rate (a high activation energy can make a feasible reaction so slow that nothing is seen), and a small positive value can be reversed by concentrations far from 1.00 mol dm−3.

6. The Nernst equation 2D · 24.2

E° is the electrode potential at 1.00 mol dm−3. Change the concentrations and the potential shifts: more of the oxidised species makes the half-cell more willing to accept electrons, so E moves positive; more of the reduced species moves it negative. The Nernst equation puts a number on it, E = E° + (0.059 / z) log([oxidised] / [reduced]), where z is the number of electrons in the half-equation.

Half-cell

[oxidised] / [reduced]
log OF THE RATIO
0.059 / z
E
WORKING
For a metal/metal-ion electrode the reduced species is the solid metal, so the ratio is just the ion concentration in mol dm−3. Each tenfold change in the ratio shifts E by 0.059 / z volts: 59 mV for a one-electron system, about 30 mV for a two-electron one. Temperature is taken as 298 K throughout.
TheLucidSTEM · Cambridge International A Level Chemistry 9701 · Topic 24 Electrochemistry. Every scene runs in the browser; drag to rotate 3D scenes, wheel to zoom. Values are standard textbook data rounded for teaching.

About this lab: Electrode potentials and electrolysis

Six interactive simulations for Cambridge A Level Chemistry 9701 topic 24 Electrochemistry: an animated electrolysis cell for molten and aqueous electrolytes with the half-equations at each electrode and the role of concentration and electrode potential in deciding which ion is discharged, Q = It and the Faraday constant worked through to the mass of metal or volume of gas produced together with the copper electrolysis that gives the Avogadro constant, the standard hydrogen electrode in 3D connected through a salt bridge to a metal or ion-ion half-cell to measure a standard electrode potential, an electrochemical cell built from any two Data Booklet half-cells showing E cell, the direction of electron flow and the overall equation, a feasibility checker comparing an oxidising agent with a reducing agent including the kinetic and non-standard-condition limitations, and the Nernst equation with E plotted against the log of the concentration ratio.

Six simulations covering Topic 24: an electrolysis cell where you choose the electrolyte and watch which ion is discharged at each electrode; Q = It and the Faraday constant turned into a mass of copper or a volume of hydrogen, and the copper experiment that gives the Avogadro constant; the standard hydrogen electrode wired to a second half-cell to measure E°; a cell built from any two half-cells with the electron flow, the positive electrode and the overall equation; a feasibility checker for any oxidising agent against any reducing agent; and the Nernst equation, with E redrawn as the concentrations change.

Electrode potentials and electrolysis is a free, browser-based simulation for Cambridge International AS & A Level Chemistry 9701 (topic 24 Electrochemistry). The course is assessed in Paper 1 (Multiple Choice (AS)), Paper 2 (AS Structured), Paper 3 (Advanced Practical), Paper 4 (A Level Structured), Paper 5 (Planning, Analysis, Evaluation). Syllabus for examination in 2025-2027. There are 6 tabs, each a self-contained experiment with its own controls and live readings, and nothing to install: it runs on a laptop, tablet or classroom projector.

Syllabus coverage

Full syllabus map: A Level Chemistry 9701 topic 24.

How to use this simulation

  1. 1. Which ion is discharged? An electrolyte conducts because its ions can move.
  2. 2. Q = It and the Faraday constant. The amount of product at an electrode depends only on how much charge has passed.
  3. 3. The standard hydrogen electrode. A single half-cell has no measurable voltage on its own; a voltmeter needs two electrodes.
  4. 4. Which way do the electrons go? Connect any two half-cells and the one with the more positive E° becomes the positive electrode: reduction happens...
  5. 5. Feasible, but will it happen? Lay the half-equations out on a ladder of E° values.
  6. 6. The Nernst equation. E° is the electrode potential at 1.00 mol dm−3.
  7. The buttons at the end of the tab strip give the scene the whole window (Full screen, Hide controls) and, on a dark stage, a projector-friendly palette (Light scene). Many scenes also have drag handles: drag them to change the set-up directly.

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