Chemistry · Year 11 · Module 3 · Lesson 8
HSC Exam Practice
Redox Reactions & Oxidation States
Short answer
1.Short answer
Define oxidation using the modern electron-transfer definition.
Distinguish between an oxidant and a reductant, with reference to electron gain or loss in each case.
Outline the rules for assigning oxidation states to oxygen and hydrogen in compounds, including the exceptions to each rule.
For the reaction: Mg(s) + 2HCl(aq) → MgCl2(aq) + H2(g)
Identify the species that is oxidised and the species that is reduced. For each, state the oxidation state change and name the species as either the oxidant or the reductant.
Explain why the oxidation state of sulfur in SO42− is +6. Show your algebraic working.
Write a balanced half-equation for the oxidation of iron(II) ions to iron(III) ions in aqueous solution. Verify your half-equation with an atom check and a charge check.
Data response
2.Data response — bleach concentration and chlorine oxidation states
The graph below shows the percentage of stain molecules destroyed by bleach solutions over a 10-minute period at three different hypochlorite ion (OCl−) concentrations. The active redox process is the oxidation of chromophore molecules by OCl−.
(a) Describe the trend shown for all three concentrations, and compare the time taken for each to destroy 40% of stain molecules.
(b) Account for the difference in rate of stain destruction between the 0.5% and 3.0% OCl− solutions, using your understanding of oxidant concentration and electron transfer in redox reactions.
3.Data response — combining half-equations for the permanganate titration
The two half-equations for the reaction of Fe2+ with permanganate (MnO4−) in acidic solution are given below.
Oxidation: Fe2+(aq) → Fe3+(aq) + e−
Reduction: MnO4−(aq) + 8H+(aq) + 5e− → Mn2+(aq) + 4H2O(l)
(a) State the oxidation states of Mn in MnO4− and Mn2+. Identify, with reasoning, which species is the oxidant in this reaction.
(b) Combine the two half-equations to produce the balanced overall ionic equation. Show how you balance the electron count.
(c) Verify your combined equation with a charge check.
Extended response
4.Extended response
Evaluate the claim that “household bleach (sodium hypochlorite, NaOCl) cannot be considered an oxidising agent because it contains no molecular oxygen (O2).” In your response, refer to the modern definition of oxidation and reduction, the oxidation state of chlorine in the relevant species, and the reduction half-equation for OCl− in alkaline solution.
Chemistry · Year 11 · Module 3 · Lesson 8
Answer Key & Marking Guidelines
Section 1 · Short answer · 1 mark · Band 3
Sample response. Oxidation is the loss of electrons by a species during a chemical reaction.
Marking notes. 1 mark for “loss of electrons” (OIL RIG). Do not accept “reaction with oxygen” alone.
Section 1 · Short answer · 2 marks · Band 3
Sample response. An oxidant (oxidising agent) is the species that gains electrons in a redox reaction; it is itself reduced. A reductant (reducing agent) is the species that loses electrons; it is itself oxidised. The oxidant causes the other species to be oxidised by accepting its electrons.
Marking notes. 1 mark for oxidant = gains electrons / is reduced. 1 mark for reductant = loses electrons / is oxidised. Must be phrased with reference to electron gain/loss.
Section 1 · Short answer · 3 marks · Band 3
Sample response. Oxygen is usually assigned an oxidation state of −2 in compounds. Exception: in peroxides (e.g. H2O2), oxygen is −1. Hydrogen is usually assigned +1 in compounds. Exception: in metal hydrides (e.g. NaH), hydrogen is −1.
Marking notes. 1 mark for O = −2 in compounds. 1 mark for the O exception (peroxides, O = −1). 1 mark for H = +1 in compounds with the H exception (metal hydrides, H = −1). Award 2 marks if only one exception given alongside both standard rules.
Section 1 · Short answer · 4 marks · Band 4
Sample response. Mg: oxidation state changes from 0 (Mg metal) to +2 (in MgCl2) — an increase → Mg is oxidised → Mg is the reductant. [1 mark for Mg identified as oxidised with ON change 0 → +2; 1 mark for correctly naming Mg as reductant.] H (in HCl, H = +1): changes to 0 (in H2) — a decrease → H+ is reduced → H+ (from HCl) is the oxidant. [1 mark for H+ identified as reduced with ON change +1 → 0; 1 mark for correctly naming H+ as oxidant.]
Marking notes. 1m — Mg oxidised, ON change 0 → +2; 1m — Mg named as reductant; 1m — H+ (or HCl) reduced, ON change +1 → 0; 1m — H+ named as oxidant. Cl is a spectator (ON = −1 throughout).
Section 1 · Short answer · 2 marks · Band 3
Sample response. In SO42−, O = −2 (Rule 3). Four oxygen atoms contribute 4 × (−2) = −8. The overall charge of the ion is −2. Setting up the equation: S + (−8) = −2, so S = −2 + 8 = +6. The oxidation state of S in SO42− is +6.
Marking notes. 1 mark for correctly setting up the algebraic equation (S + 4(−2) = −2). 1 mark for correct answer S = +6.
Section 1 · Short answer · 2 marks · Band 4
Sample response. Fe2+(aq) → Fe3+(aq) + e−. Atom check: 1Fe on each side. ✓ Charge check: left = +2; right = (+3) + (−1) = +2. ✓
Marking notes. 1 mark for the correct half-equation with electrons on the right (oxidation). 1 mark for both a correct atom check AND a correct charge check (both checks required for this mark).
Section 2 · Data response · 5 marks · Band 4–5
Sample response (a). All three concentrations show an increasing percentage of stain molecules destroyed over time. The 3.0% solution destroys stain molecules fastest — reaching 40% destruction by approximately 4 minutes — while the 1.0% solution reaches 40% at approximately 5–6 minutes, and the 0.5% solution has not reached 40% by 10 minutes (only approximately 35%). Award: 1 mark for correctly describing the general increasing trend for all three; 1 mark for comparing the time to 40% destruction with appropriate data reference for at least two concentrations.
Sample response (b). The 3.0% OCl− solution has a higher concentration of oxidant molecules than the 0.5% solution. A higher oxidant concentration means more OCl− ions are available per unit volume per unit time to accept electrons from chromophore (stain) molecules. The rate of electron transfer from chromophore to OCl− is therefore greater, destroying more stain molecules in the same time. The 0.5% solution has fewer OCl− molecules available, so electron-transfer events occur less frequently and stain destruction proceeds more slowly. Award: 1 mark for identifying higher [OCl−] in the 3.0% solution; 1 mark for explaining the link between oxidant concentration and rate/frequency of electron-transfer events; 1 mark for explicitly connecting this to the observed difference in stain destruction rate (not just stating “more concentrated = faster”).
Section 2 · Data response · 6 marks · Band 4–5
Sample response (a). In MnO4−: charge = −1, O = −2, so 4(−2) + Mn = −1 → Mn = +7. In Mn2+: oxidation state = +2 (monatomic ion). Mn changes from +7 → +2 (a decrease). A decrease in oxidation state indicates reduction (RIG). MnO4− is therefore the oxidant — it gains electrons and is reduced. [2 marks: 1 for correct ON of Mn with working; 1 for identifying MnO4− as oxidant with RIG reasoning.]
Sample response (b). Multiply oxidation half by 5: 5Fe2+(aq) → 5Fe3+(aq) + 5e−. This matches the 5e− in the reduction half. Add and cancel 5e−: 5Fe2+(aq) + MnO4−(aq) + 8H+(aq) → 5Fe3+(aq) + Mn2+(aq) + 4H2O(l). [2 marks: 1 for correctly multiplying Fe half by 5 and cancelling electrons; 1 for the balanced overall equation.]
Sample response (c). Left: 5(+2) + (−1) + 8(+1) = 10 − 1 + 8 = +17. Right: 5(+3) + (+2) + 0 = 15 + 2 = +17. Charge balanced. ✓ [2 marks: 1 for calculating left-side total charge correctly; 1 for calculating right-side total charge and confirming balance.]
Section 3 · Extended response · 7 marks · Band 5–6
Sample response. The claim is incorrect. The modern definition of an oxidising agent does not require molecular oxygen (O2) to be present; it requires only that the species accepts electrons from another species, causing that other species to be oxidised. This is the electron-transfer definition — summarised by OIL RIG (Oxidation Is Loss, Reduction Is Gain of electrons) — which supersedes the older “reaction with oxygen” definition.
In household bleach, the active species is OCl− (hypochlorite ion), formed when NaOCl dissolves in water. The oxidation state of chlorine in OCl− is calculated as: charge = −1, O = −2, so Cl + (−2) = −1 → Cl = +1. The oxidation state of chlorine in the product Cl− is −1. The change is +1 → −1, a decrease of 2. A decrease in oxidation number indicates reduction (RIG). The reduction half-equation in alkaline solution is: OCl−(aq) + H2O(l) + 2e− → Cl−(aq) + 2OH−(aq). This half-equation shows OCl− accepting 2 electrons — it is being reduced. A species that is reduced in a redox reaction is, by definition, the oxidant (oxidising agent). OCl− causes whatever it reacts with (e.g. stain molecules or bacterial cell walls) to lose electrons, i.e. to be oxidised. The absence of O2 from this mechanism is irrelevant: the electron-transfer criterion is fully met. The claim therefore conflates the old oxygen-combination definition with the modern electron-transfer definition, and is rejected.
Marking criteria.
- 1 mark — States an explicit overall evaluative judgement rejecting the claim.
- 1 mark — Explains that the modern definition of an oxidising agent is based on electron gain (not involvement of O2), referencing OIL RIG or electron-transfer explicitly.
- 1 mark — Correctly calculates the oxidation state of Cl in OCl− (+1) with algebraic working shown.
- 1 mark — States the oxidation state of Cl in Cl− (−1) and identifies the decrease in oxidation state as evidence of reduction.
- 1 mark — Writes the balanced reduction half-equation for OCl− in alkaline solution (or correctly cites/verifies the given equation with atom and charge checks).
- 1 mark — Explains, using the half-equation, that OCl− accepts electrons and therefore causes the other species to be oxidised — satisfying the definition of an oxidising agent without O2 being involved.
- 1 mark — Clearly distinguishes the old oxygen-combination definition from the modern electron-transfer definition and explicitly explains why the modern definition makes the claim incorrect.