# Redox Processes (IB)
Redox reactions involve the transfer of electrons. The IB covers oxidation states, half-equations, electrochemical cells, electrolysis, and at HL, standard electrode potentials and the Nernst equation.
1. Oxidation States
Rules: element = 0, O = −2, H = +1, sum = 0 (compound) or charge (ion).
Oxidation: increase in oxidation state / loss of electrons Reduction: decrease in oxidation state / gain of electrons OIL RIG: Oxidation Is Loss, Reduction Is Gain
2. Balancing Redox Equations
Half-equation method:
- Write separate oxidation and reduction half-equations
- Balance atoms (use H₂O for O, H⁺ for H)
- Balance charges with electrons
- Equalise electrons and combine
- In basic solution: add OH⁻ to neutralise H⁺
3. Voltaic (Galvanic) Cells
Convert chemical energy → electrical energy from spontaneous redox reactions.
- Anode: oxidation occurs (negative terminal)
- Cathode: reduction occurs (positive terminal)
- Salt bridge: completes circuit, maintains electrical neutrality
- Electron flow: anode → external circuit → cathode
4. Standard Electrode Potentials (HL)
- Positive → spontaneous
- More positive → stronger oxidising agent
- More negative → stronger reducing agent
5. Electrolysis
Uses electricity to drive non-spontaneous redox reactions.
- Cations → cathode (reduction)
- Anions → anode (oxidation)
For aqueous solutions:
- Cathode: metal deposited if less reactive than H; otherwise H₂
- Anode: halogen if halide present; otherwise O₂
6. Practice Questions
- Assign oxidation states to all atoms in .
- Balance: in acidic solution.
- Calculate for Zn/Cu cell (: Zn = −0.76 V, Cu = +0.34 V).
- Predict products of electrolysis of aqueous NaCl.
- Explain why a salt bridge is needed in a voltaic cell.
Want to check your answers and get step-by-step solutions?
Summary
- Redox: electron transfer; OIL RIG
- Voltaic cells: spontaneous redox → electricity; anode = oxidation, cathode = reduction
- ; positive = spontaneous
- Electrolysis: electricity drives non-spontaneous reactions
