Construct the half-equation for the reduction of the chlorate(I) ion, ClO⁻, to chloride ions in acid solution.

The half-equation is ClO⁻ + 2H⁺ + 2e⁻ → Cl⁻ + H₂O. The single oxygen atom leaves as one water molecule, which needs two hydrogen ions to supply its hydrogen. Two electrons are then added on the left so that the charge is −1 + 2 − 2 = −1 on each side, matching chlorine falling from +1 in ClO⁻ to −1 in Cl⁻.

What is the half-equation for the oxidation of thiosulfate ions to tetrathionate ions?

2S₂O₃²⁻ → S₄O₆²⁻ + 2e⁻. Two thiosulfate ions are needed to supply the four sulfur atoms, and two electrons balance the charge, since −4 on the left equals −2 − 2 on the right.

Why do hydrogen ions appear in the half-equation for the reduction of manganate(VII)?

The manganate(VII) ion carries four oxygen atoms which are not present in the Mn²⁺ product. Those oxygen atoms leave as water, and the hydrogen needed to form that water is supplied by the acid, so hydrogen ions must appear on the left of the equation.

Why must a solution of dichromate(VI) or manganate(VII) be acidified before it can act as an oxidising agent in these ways?

Both half-equations consume a large number of hydrogen ions, eight for each manganate(VII) ion and fourteen for each dichromate(VI) ion. Without a plentiful supply of acid the reduction to Mn²⁺ or Cr³⁺ cannot take place.

WJEC A-Level Chemistry 1410QS

Formulae and Equations

Topic overview Charges on common ions Building formulae for ionic and molecular compounds Assigning oxidation numbers Using oxidation numbers to follow redox changes Balancing equations and using state symbols Ionic and half equations

Basic Ideas About Atoms

Topic overview Radioactive decay and nuclear equations Alpha, beta and gamma radiation Half-life, dating and the uses of radioisotopes: half-life of radioactive decay Half-life, dating and the uses of radioisotopes: adverse consequences for living cells Ionisation energies and electronic structure Orbitals and the filling of sub-shells Atomic spectra and the energy of light: atomic emission spectrum of the hydrogen atom Atomic spectra and the energy of light: relationship between energy and frequency Atomic spectra and the energy of light: significance of the frequency

Chemical Calculations

Topic overview Relative masses and the mass spectrometer: relative atomic Relative masses and the mass spectrometer: how a mass spectrometer works Relative masses and the mass spectrometer: molecular ion The mole, the Avogadro constant and molar mass: relative mass terms and simple mass spectra The mole, the Avogadro constant and molar mass: moles and percentage composition by mass Empirical and molecular formulae Concentration, solubility and titration calculations: concentration in mol dm-3 and in g dm-3 Concentration, solubility and titration calculations: stoichiometry and the limiting reagent Concentration, solubility and titration calculations: titration calculations and estimating a titre Gas volumes and the ideal gas equation Yield, atom economy and experimental uncertainty: concepts of atom economy and percentage yield Yield, atom economy and experimental uncertainty: how to estimate the percentage error

Bonding

Topic overview Ionic bonds and covalent bonds: ionic bonding in terms of ion formation Ionic bonds and covalent bonds: covalent bonding and forces Electronegativity, polarity and in-between bonds: concepts of electronegativity and bond polarity Electronegativity, polarity and in-between bonds: forces Forces between molecules Hydrogen bonding Shapes of molecules and ions: VSEPR principle and its use Shapes of molecules and ions: bond angles associated with linear

Solid Structures

Topic overview Ionic crystals: sodium chloride and caesium chloride Giant covalent structures: diamond and graphite Simple molecular solids: iodine and ice Metals and the electron sea Using structure to explain physical properties

The Periodic Table

Topic overview How the Periodic Table is organised Oxidation and reduction as electron transfer Trends across periods and down groups Group 2: reactions, trends and the reasons behind them — reactions with oxygen, water and dilute acid Group 2: reactions, trends and the reasons behind them — trends down the group Group 2: reactions, trends and the reasons behind them — thermal stability of the carbonates Group 2: reactions, trends and the reasons behind them — oxides and hydroxides Identifying ions, making salts and gravimetric analysis: identifying cations with sodium hydroxide Identifying ions, making salts and gravimetric analysis: preparing a soluble salt from an acid Group 7: the halogens — physical properties and the trend in volatility Group 7: the halogens — reactions of the halogens with metals Group 7: the halogens — displacement reactions and the trend Group 7: the halogens — halide ions as reducing agents, uses of chlorine and the chlorate equilibrium

Simple Equilibria and Acid-Base Reactions

Topic overview Reversible reactions and dynamic equilibrium Le Chatelier's principle and shifting the position of equilibrium The equilibrium constant Kc Acids, bases, salts and neutralisation pH, strong acids and weak acids Acid-base titrations and their calculations

Thermochemistry

Topic overview Enthalpy changes and their definitions Calculating enthalpy changes from experimental measurements Determining enthalpy changes in the laboratory Hess's law and energy cycles Average bond enthalpies

Rates of Reaction

Topic overview Collision theory and the conditions that change rate Measuring rate and relating it to concentration Energy profiles and activation energy Temperature and the Boltzmann distribution Catalysts and how they work Following reactions in the laboratory

The Wider Impact of Chemistry

Topic overview Social and economic consequences of chemical manufacture and energy supply Environmental consequences of chemical processes and energy production Green chemistry and sustainable practice

Organic Compounds

Topic overview Drawing and reading organic structures Naming organic compounds Chain length, functional groups and physical properties Structural isomerism Electrophiles, nucleophiles, radicals and bond fission

Hydrocarbons

Topic overview Alkane bonding, combustion and fossil fuels: combustion reaction of alkanes and benefits Alkane bonding, combustion and fossil fuels: combustion calculations and acid rain Radical substitution of alkanes The C=C bond and why alkenes are reactive E–Z isomerism in alkenes Electrophilic addition, Markovnikov's rule and testing for alkenes: mechanism of electrophilic addition Electrophilic addition, Markovnikov's rule and testing for alkenes: Markovnikov's rule and the bromine water test Electrophilic addition, Markovnikov's rule and testing for alkenes: testing for a C=C bond Hydrogenation and addition polymers: conditions required Hydrogenation and addition polymers: nature of addition polymerisation

Halogenoalkanes

Topic overview Nucleophilic substitution by hydroxide ions Elimination to form alkenes Reactivity of the carbon–halogen bond and the silver nitrate test Uses of halogenoalkanes, CFCs and the ozone layer: uses of halogenoalkanes and CFCs Uses of halogenoalkanes, CFCs and the ozone layer: radical mechanism Uses of halogenoalkanes, CFCs and the ozone layer: replacements for CFCs Heating under reflux in the laboratory

Alcohols and Carboxylic Acids

Topic overview Two routes to ethanol: hydration and fermentation — hydration of ethene Two routes to ethanol: hydration and fermentation — fermentation Two routes to ethanol: hydration and fermentation — comparing the two routes on rate Classifying alcohols and dehydrating them Oxidising alcohols to aldehydes, ketones and acids Chemical tests for alcohols and carboxylic acids Carboxylic acids, bases and salts Making an ester and separating it by distillation: esterification Making an ester and separating it by distillation: carrying out the preparation Making an ester and separating it by distillation: separating and purifying Making an ester and separating it by distillation: yield

Instrumental Analysis

Topic overview Reading a mass spectrum Infrared spectra and functional groups NMR spectra and atomic environments Putting the three techniques together

Redox and Standard Electrode Potential

Topic overview Electron transfer and oxidation numbers Half-equations, half-cells and cell diagrams The hydrogen electrode and standard electrode potentials Cell EMF and the feasibility of reactions The hydrogen fuel cell

Redox Reactions

Topic overview Building ion–electron half-equations Combining half-equations into full equations Copper, iodide and thiosulfate Carrying out and calculating a redox titration: procedure for a manganate titration Carrying out and calculating a redox titration: redox titration calculations

Chemistry of the P-Block

Topic overview Amphoteric behaviour of aluminium and lead Stability of oxidation states down Groups 3, 4 and 5: increasing stability of the inert pair cations Stability of oxidation states down Groups 3, 4 and 5: change in relative stability Valence shells that break the octet rule: how some Group 3 elements can form compounds Valence shells that break the octet rule: structure and bonding in Al2Cl6 and formation Boron nitride: two structures, two sets of properties Group 4 oxides and chlorides, and lead in solution: structure Group 4 oxides and chlorides, and lead in solution: hydrolysis of the Group 4 chlorides Group 4 oxides and chlorides, and lead in solution: chloride hydrolysis and lead(II) precipitates Group 4 oxides and chlorides, and lead in solution: distinguishing lead from silver ions Chlorine, chlorate and the sodium halides: chlorine with water and with cold and hot alkali Chlorine, chlorate and the sodium halides: bleaching and bactericidal action of Cl2 Chlorine, chlorate and the sodium halides: differences in behaviour of NaCl

Chemistry of the D-Block Transition Metals

Topic overview Variable oxidation states and the colours of their solutions: how the d-block elements attain various Variable oxidation states and the colours of their solutions: most important oxidation states of Cr Complex ions: ligands, coordination number and shape Why transition metal complexes are coloured Ligand exchange and changes in coordination number Transition metals as catalysts: why transition metals Transition metals as catalysts: variable oxidation state Transition metals as catalysts: heterogeneous catalysis Transition metals as catalysts: surface area Transition metal ions with aqueous hydroxide

Chemical Kinetics

Topic overview Following a reaction by sampling and quenching Finding the order of a reaction from experimental results The rate equation and the rate constant Rate-determining steps and reaction mechanisms Temperature, catalysts and the Arrhenius equation

Enthalpy Changes for Solids and Solutions

Topic overview Defining the enthalpy changes Born-Haber cycles for ionic compounds Dissolving: lattice breaking against hydration What the enthalpy of formation says about stability

Entropy and Feasibility of Reactions

Topic overview Entropy as the freedom of particles Comparing entropy across states and reactions Calculating entropy changes Gibbs free energy change Feasibility, temperature and spontaneous endothermic change

Equilibrium Constants

Topic overview Writing equilibrium constant expressions and deriving their units Calculating Kc and equilibrium amounts Partial pressures and Kp calculations Temperature, magnitude and the position of equilibrium

Acid-Base Equilibria

Topic overview Proton transfer and conjugate pairs Strong and weak acids: Ka and pKa Water, Kw and the pH scale pH calculations for acids and alkalis: how to use pH pH calculations for acids and alkalis: strong bases, dilution and mixtures Buffers: how they hold pH steady and why they matter Titrations: curve shapes, salt pH and choosing an indicator — pH curve shapes for strong and weak acids and bases Titrations: curve shapes, salt pH and choosing an indicator Titrations: curve shapes, salt pH and choosing an indicator — how an indicator works and choosing one Titrations: curve shapes, salt pH and choosing an indicator — using a pH probe

Stereoisomerism

Topic overview Structural isomerism and stereoisomerism compared E‒Z isomerism and the priority rules Chiral centres, enantiomers and racemic mixtures Optical activity and plane-polarised light

Aromaticity

Topic overview Benzene: shape, bonding and delocalisation Aromatic stability and resistance to addition Electrophilic substitution: nitration, halogenation and alkylation How ring and substituent affect each other

Alcohols and Phenols

Topic overview Making primary and secondary alcohols Reactions of primary and secondary alcohols Phenol: acidity and characteristic reactions Recognising a phenol

Aldehydes and Ketones

Topic overview Making aldehydes and ketones from alcohols Distinguishing aldehydes from ketones Reduction of carbonyl compounds with NaBH₄ Nucleophilic addition of hydrogen cyanide 2,4-dinitrophenylhydrazine as a test for a carbonyl group The triiodomethane test

Carboxylic Acids and Their Derivatives

Topic overview Comparing the acidity of carboxylic acids, phenols, alcohols and water Making carboxylic acids by oxidation Reduction and decarboxylation of carboxylic acids: reduction of carboxylic acids using LiAlH₄ Reduction and decarboxylation of carboxylic acids: decarboxylation of carboxylic acids Esters and acid chlorides Turning acids and halogenoalkanes into amides and nitriles Hydrolysis and reduction of nitriles and amides

Amines

Topic overview Preparing aliphatic and aromatic amines The basicity of amines Ethanoylation of primary amines Primary amines and cold nitric(III) acid Coupling reactions and azo dyes: coupling of benzenediazonium salts with phenols Coupling reactions and azo dyes: role of the —N=N— chromophore in azo dyes The origin of colour

Amino Acids, Peptides and Proteins

Topic overview Structure and classification of α-amino acids Zwitterions, amphoteric character and physical properties Peptide links: dipeptides, polypeptides and proteins Levels of protein structure and the bonds that hold them Proteins at work: enzymes and biological function

Organic Synthesis and Analysis

Topic overview Planning a synthesis as a sequence of reactions Working up a preparation: separation and purification Melting temperature as a test of purity Addition and condensation polymerisation: polyesters and polyamides Polymers: hydrolysis, properties and identifying repeat units High-resolution ¹H NMR and the elucidation of structure: low- and high-resolution proton NMR High-resolution ¹H NMR and the elucidation of structure: chemical shift, TMS, solvents and D₂O exchange High-resolution ¹H NMR and the elucidation of structure: combining mass spectra and NMR to identify compounds High-resolution ¹H NMR and the elucidation of structure: combining NMR with mass spectrometry Chromatography and the composition of mixtures

Practical Skills and Techniques

Topic overview Measuring mass, volume, time and temperature Standard solutions and titration technique Indicators and acid–base titration curves Heating, refluxing, distilling and purifying: Heating Heating, refluxing, distilling and purifying: purifying Melting temperature, chromatography and pH measurement Electrochemical cells, rate methods and working safely: Electrochemical cells Electrochemical cells, rate methods and working safely: rate methods and working safely

Planning, Analysis and Evaluation

Topic overview Planning an investigation and controlling variables Recording observations and presenting data Graphs, gradients and processing data Errors, uncertainty, accuracy and precision Evaluating a method and suggesting improvements Research and referencing

Core Experiments and Their Chemistry

Topic overview Gravimetric and acid–base analysis Enthalpy and rate experiments: Enthalpy Enthalpy and rate experiments: rate experiments Redox titrations and electrochemical cells Equilibrium constants and following a titration with a pH probe Organic synthesis, separation and identification: Organic synthesis Organic synthesis, separation and identification: identification tests and chromatography

Mathematical Skills in Chemistry

Topic overview Units, standard form and proportion in chemical calculation: volume, equilibrium, rate and energy units Units, standard form and proportion in chemical calculation: standard form Units, standard form and proportion in chemical calculation: proportion Units, standard form and proportion in chemical calculation: checking answers, buffers, rate constants and units Significant figures, means and uncertainty in experimental data: significant figures in multiplication Significant figures, means and uncertainty in experimental data: relative atomic mass as a weighted mean Significant figures, means and uncertainty in experimental data: absolute and percentage uncertainty Symbols, rearranging equations and logarithms: chemical symbols and what each one asserts Symbols, rearranging equations and logarithms: rearranging an equation Symbols, rearranging equations and logarithms: substituting into equations for Kc, enthalpy and pH Symbols, rearranging equations and logarithms: logarithms, the Arrhenius equation and rearranging formulae Graphs: plotting, gradients, intercepts and tangents — reading a spectrum Graphs: plotting, gradients, intercepts and tangents — reaction order from data and plotting good graphs Graphs: plotting, gradients, intercepts and tangents — Arrhenius plots, zero-order graphs and tangents Graphs: plotting, gradients, intercepts and tangents — initial rates from tangents and interpreting graphs Shape, symmetry and three-dimensional structure: Shape Shape, symmetry and three-dimensional structure: symmetry

Redox Reactions

5 subtopics
15 things to know
A2 Unit 3

What Redox Reactions covers

Redox Reactions is examined on A2 Unit 3 of WJEC Chemistry, Physical and Inorganic Chemistry. 81 recall questions across 5 subtopics.

Where it is assessed

A2 Unit 3

Physical and Inorganic Chemistry.

Check the WJEC specification ↗

The 5 subtopics

Each one has its own page.

What you need to know

Answer each one before you reveal it.

Your recallNot started

Key term

How do you construct a half-equation for a species reacting in acid solution?

Key term

What is the half-equation for the reduction of the manganate(VII) ion to Mn²⁺ in acid solution?

Key term

What is the half-equation for the reduction of VO₂⁺ to VO²⁺ in acid solution?

Numbers

Combine the dichromate(VI) half-equation with the oxidation of iron(II).

Key term

What is the overall equation for the reaction of acidified dichromate(VI) with iodide ions?

Key term

What is the overall equation for the reaction of acidified manganate(VII) with iodide ions?

Key term

What is seen when an excess of potassium iodide solution is added to a solution of a copper(II) salt?

Key term

Use oxidation numbers to show that the reaction of copper(II) with iodide is a redox reaction.

Numbers

Why is an excess of potassium iodide added when copper(II) ions are treated with iodide?

Key term

Why is no indicator needed in a titration with potassium manganate(VII)?

Key term

Which acid is used to acidify the flask in a manganate(VII) titration, and why not hydrochloric acid?

Key term

Why is nitric acid not used to acidify a manganate(VII) titration?

Numbers

25.0 cm³ of an iron(II) solution requires 22.40 cm³ of 0.0200 mol dm⁻³ potassium manganate(VII). Calculate the concentration of the iron(II) solution.

Numbers

Calculate the volume of 0.0200 mol dm⁻³ potassium manganate(VII) needed to react with 25.0 cm³ of 0.0500 mol dm⁻³ sodium ethanedioate in acid solution.

Numbers

Calculate the volume of 0.100 mol dm⁻³ iron(II) sulfate solution that would react with 25.0 cm³ of 0.0250 mol dm⁻³ potassium dichromate(VI) in acid solution.

Take Redox Reactions further

The same content, four other ways.

Commonly confused

Pairs that lose marks when they are blurred together.

An oxidising agent vs A reducing agent
An oxidising agent: a species that takes electrons from another and is itself reduced. A reducing agent: a species that gives electrons to another and is itself oxidised.
The standard electrode potential vs The cell EMF
The standard electrode potential: the voltage of a half-cell measured against the standard hydrogen electrode. The cell EMF: the difference between the two electrode potentials in a complete cell.

Questions from this topic

Each one with the model answer underneath.

1
How do you construct a half-equation for a species reacting in acid solution?
Model answer
Write the species that changes on each side and balance the atoms of the element being oxidised or reduced. Add water molecules to balance the oxygen atoms, then add hydrogen ions to balance the hydrogen atoms. Finally add electrons to whichever side is needed so that the total charge is the same on both sides.
2
What is the half-equation for the reduction of the manganate(VII) ion to Mn²⁺ in acid solution?
Model answer
MnO₄⁻ + 8H⁺ + 5e⁻ → Mn²⁺ + 4H₂O. Four water molecules balance the four oxygen atoms, eight hydrogen ions balance the hydrogen, and five electrons make the charge +2 on both sides, since −1 + 8 − 5 = +2.
3
Construct the half-equation for the reduction of the chlorate(I) ion, ClO⁻, to chloride ions in acid solution.
Model answer
The half-equation is ClO⁻ + 2H⁺ + 2e⁻ → Cl⁻ + H₂O. The single oxygen atom leaves as one water molecule, which needs two hydrogen ions to supply its hydrogen. Two electrons are then added on the left so that the charge is −1 + 2 − 2 = −1 on each side, matching chlorine falling from +1 in ClO⁻ to −1 in Cl⁻.
4
What is the half-equation for the oxidation of thiosulfate ions to tetrathionate ions?
Model answer
2S₂O₃²⁻ → S₄O₆²⁻ + 2e⁻. Two thiosulfate ions are needed to supply the four sulfur atoms, and two electrons balance the charge, since −4 on the left equals −2 − 2 on the right.
5
Why do hydrogen ions appear in the half-equation for the reduction of manganate(VII)?
Model answer
The manganate(VII) ion carries four oxygen atoms which are not present in the Mn²⁺ product. Those oxygen atoms leave as water, and the hydrogen needed to form that water is supplied by the acid, so hydrogen ions must appear on the left of the equation.
6
Why must a solution of dichromate(VI) or manganate(VII) be acidified before it can act as an oxidising agent in these ways?
Model answer
Both half-equations consume a large number of hydrogen ions, eight for each manganate(VII) ion and fourteen for each dichromate(VI) ion. Without a plentiful supply of acid the reduction to Mn²⁺ or Cr³⁺ cannot take place.

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Redox Reactions revision questions

What does Redox Reactions cover in WJEC A-Level Chemistry?: 5 subtopics: building ion–electron half-equations, combining half-equations into full equations, copper, iodide and thiosulfate, carrying out and calculating a redox titration: procedure for a manganate titration and carrying out and calculating a redox titration: redox titration calculations. Each one has its own page with questions and model answers.
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