OCR A-Level Chemistry B H433
Development of Practical Skills in Chemistry
Elements of Life
Developing Fuels
Elements From the Sea
The Ozone Story
What's in a Medicine?
The Chemical Industry
Polymers and Life
Oceans
Developing Metals
Colour by Design
Chemical Literacy
Mathematical Skills in Chemistry
Developing Metals
- 18 subtopics
- 53 things to know
- Components 01, 02 and 03
What Developing Metals covers
The storyline that carries electrochemistry and the transition elements: redox titrations, balancing half-equations in acid, electrochemical cells and standard electrode potentials, rusting, and the complexes, colours and catalysis of the d-block.
Where it is assessed
Components 01, 02 and 03
Storyline content, drawn on by all three written papers.
Check the OCR specification ↗The 18 subtopics
Each one has its own page.
- Manganate(VII) titrations and their calculationsRecall questions on why manganate(VII) is self-indicating, which acid is used and why the others are not, and the calculations with iron(II), ethanedioate and peroxide.Open →
- Thiosulfate titrations, recording results and good techniqueRecall questions on the copper(II) and iodine route, when starch is added, concordant titres, and why the burette but not the flask is rinsed with solution.Open →
- Shapes of complexes and coordination numberRecall questions on why coordination number is not always the ligand count, and the shapes and bond angles for four and six coordination.Open →
- Balancing redox equations involving acid-base reactionsRecall questions on the manganate(VII) and dichromate(VI) half-equations, why the electron counts are what they are, and combining halves into a full equation.Open →
- Simple electrochemical cellsRecall questions on setting up a metal half-cell, the salt bridge, the high-resistance voltmeter, and the standard conditions.Open →
- Action of an electrochemical cellRecall questions on which electrode is negative and why, the half-equation at each, and what happens to the electrode masses and the solution as the cell runs.Open →
- Standard electrode potentials and calculating E°cellRecall questions on the definition and the hydrogen reference, what a positive or negative value means, and calculating E°cell to test feasibility.Open →
- Rusting and how it is preventedRecall questions on the two half-equations, what rust is, and how galvanising, barrier methods and cathodic protection each work.Open →
- Transition metals: definition, oxidation states and coloursRecall questions on what defines a transition element, the colours of the common aqueous ions, and the disproportionation of copper(I).Open →
- d-block electron configurations of the atoms and their ionsRecall questions on which sub-shell fills first, which electrons are lost first, and the configurations of chromium, copper and the common ions.Open →
- Why transition metals show variable oxidation statesRecall questions on the closeness of the 4s and 3d energies, why the s-block shows one state only, and which arrangements carry extra stability.Open →
- Ligands and complex ionsRecall questions on the three common monodentate ligands, why complexes carry the charges they do, and working out a complex's charge.Open →
- Coordinate bonding and what makes a ligandRecall questions on what a coordinate bond is, which atom donates, why methane cannot be a ligand, and how the bond compares with an ordinary covalent one.Open →
- Bidentate and multidentate ligands, and finding a complex's formulaRecall questions on the ethanedioate ion and EDTA, how many bind to one metal ion, and deducing a formula from a mole ratio.Open →
- Reactions of Fe2+, Fe3+ and Cu2+ with hydroxide and ammoniaRecall questions on the colour and identity of each precipitate, the ionic equations, why the iron(II) precipitate darkens, and which redissolve in excess ammonia.Open →
- Catalytic activity of transition metalsRecall questions on how a variable oxidation state allows catalysis, the two steps of the iodide and peroxodisulfate route, and adsorption strength.Open →
- Origin of colour in transition metal complexesRecall questions on d orbital splitting, why some ions are colourless, and how ligand, oxidation state and coordination number change the colour.Open →
- ColorimetryRecall questions on choosing a filter, the blank, building and using a calibration line, and why a sample above the range must be diluted.Open →
What you need to know
Answer each one before you reveal it.
What is the oxidising agent in a manganate(VII) titration, and what are its equations with iron(II) and with ethanedioate?
Why is the ethanedioate titration warmed, what is the equation with hydrogen peroxide, and why is starch added late?
Why is the coordination number not always the number of ligands, what is the bond angle in a tetrahedral complex, and what shape does a 6-coordinate complex adopt?
Why does copper(II) form a 6-coordinate complex with water but only a 4-coordinate one with chloride?
Deduce the coordination number of [Fe(C₂O₄)₃]³⁻.
Deduce the coordination number and shape of [Cr(H₂O)₄Cl₂]⁺.
What is the half-equation for manganate(VII) reduced to manganese(II), and why are exactly five electrons needed?
How are the manganate(VII) and iron(II) half-equations combined, and what is the dichromate(VI) half-equation?
How do the charges balance in the dichromate(VI) half-equation, what is its full ionic equation with iron(II), and what is the half-equation for the oxidation of ethanedioate?
Write the full ionic equation for the oxidation of hydrogen peroxide by manganate(VII) in acid.
How are a copper and a zinc half-cell set up, and what temperature and pressure count as standard?
In a zinc-copper cell which metal is the negative electrode and why, and what are the two half-equations?
What happens to the electrode masses and the solution colour as a zinc–copper cell runs, and what reaction occurs at the platinum electrode of an iron(III)/iron(II) half-cell when it is positive?
Explain in terms of electrode potentials why electrons leave the zinc half-cell rather than the copper one.
What is the hydrogen electrode equation, and what do strongly negative and strongly positive electrode potentials each mean?
Which is the negative electrode in a zinc-copper cell, and do manganate(VII) and dichromate(VI) each oxidise chloride?
What are the two half-equations for rusting, and what is the composition of rust?
Explain how a zinc coating protects iron even when the coating is scratched.
What colour is aqueous iron(III), is copper(I) coloured, and what is the equation for its disproportionation?
Which iron oxidation state is more stable in air, why should an iron(II) solution be freshly prepared before a titration, and which common reagent contains a transition metal in a high oxidation state?
Deduce the oxidation state of chromium in Cr₂O₇²⁻.
Deduce the oxidation state of manganese in MnO₄⁻.
Which sub-shell fills first in the first-row d block, which electrons are lost first, and why is copper 3d¹⁰ 4s¹?
Why does chromium have its electron configuration, how many electrons can occupy one orbital, and why do transition metals show variable oxidation states?
Which two d-electron arrangements are associated with extra stability?
Which three monodentate ligands are most common, why do the two aqua iron complexes carry different charges, and why does [CuCl₄]²⁻ carry a 2− charge?
Why does the coordination number fall from six to four when chloride ions replace the water ligands of [Cu(H₂O)₆]²⁺?
Write an equation for the ligand substitution that occurs when concentrated hydrochloric acid is added to aqueous copper(II) sulfate.
A complex has the formula [MCl₂(H₂O)₄]⁺. Deduce the oxidation state of the metal M.
How does the ethanedioate ion act as a bidentate ligand, and how many can surround one metal ion?
What are the coordination number and ligand count of [Fe(C₂O₄)₃]³⁻, and what happens when excess ammonia is added to copper?
Which atom of water donates the lone pair, what are the coordination number and shape when 1.00 × 10⁻³ mol of a metal ion combines with 3.00 × 10⁻³ mol of a bidentate ligand, and what is the coordination number with a hexadentate ligand in a 1:1 ratio?
Which atom in an ammonia molecule donates the lone pair to a metal ion?
What is seen when sodium hydroxide is added to aqueous iron(II), what is the ionic equation, and why does the green precipitate turn brown in air?
What are the ionic equations for precipitating iron(III) and copper(II) hydroxide, and what is seen?
What is seen when ammonia is added to iron(II), why does it give the same precipitates as hydroxide, and do they redissolve?
Write an equation showing ammonia acting as a base towards aqueous copper(II) ions.
How does a variable oxidation state let a transition metal ion catalyse a reaction, and what are the two steps when iron ions catalyse peroxodisulfate reacting with iodide?
Why is the peroxodisulfate and iodide reaction slow uncatalysed, and what happens if adsorption is too strong or too weak?
Which transition metals are used as catalysts in a car exhaust catalytic converter?
Which two d-block ions are colourless and why, why do we see a colour rather than darkness, and how is the energy gap related to the frequency absorbed?
What does a larger energy gap do to the wavelength absorbed, why does ammonia deepen a copper(II) solution, and how does oxidation state change the colour of aqueous iron?
How can coordination number change a copper complex's colour, why is a dilute solution paler, and why do transitions between the split d levels absorb visible rather than ultraviolet light?
Combine ΔE = hν and c = νλ to link the energy gap to the wavelength absorbed.
Why does colorimetry suit transition metal chemistry, and how is the filter chosen for a blue copper solution?
What is the blank for, why should the calibration line pass through the origin, and why dilute a sample above the range?
Why is a colorimeter unsuitable for a colourless solution?
Why is a colorimeter well suited to following the rate of a reaction continuously?
Why is nitric acid also unsuitable for acidifying a manganate(VII) titration?
Why is a rough titration carried out before the accurate ones?
What effect would rinsing the conical flask with the solution to be titrated have on the result?
What temperature and pressure are used as standard for electrode potential measurements?
Take Developing Metals further
The same content, four other ways.
Commonly confused
Pairs that lose marks when they are blurred together.
Ligand vs Coordination number
Ligand: a species donating a lone pair to form a coordinate bond with a metal ion. Coordination number: the number of coordinate bonds formed to the central metal ion.
Monodentate ligand vs Bidentate ligand
Monodentate ligand: a ligand that forms one coordinate bond to the metal ion. Bidentate ligand: a ligand that forms two coordinate bonds to the same metal ion.
Standard electrode potential vs Standard cell potential
Standard electrode potential: the potential of a half-cell measured against the standard hydrogen electrode. Standard cell potential: the difference between the two electrode potentials of a complete cell.
Questions from this topic
Each one with the model answer underneath.
- 1
What is the oxidising agent in a manganate(VII) titration, and what is the oxidation state of the manganese in it?
Model answer
The manganate(VII) ion MnO₄⁻ is the oxidising agent, and the manganese in it has oxidation state +7.
- 2
Why does a manganate(VII) titration need no added indicator?
Model answer
MnO₄⁻ is intensely purple while Mn²⁺ is almost colourless, so the reagent indicates its own end point.
- 3
Describe what you see at the end point when MnO₄⁻ is run into acidified iron(II) solution.
Model answer
The flask stays colourless or very pale until one drop gives a permanent faint pink colour.
- 4
Which acid is used to acidify a manganate(VII) titration, and why is hydrochloric acid avoided?
Model answer
Dilute sulfuric acid is used, because manganate(VII) would oxidise the chloride ions of hydrochloric acid and the titre would be too large.
- 5
Why is nitric acid also unsuitable for acidifying a manganate(VII) titration?
Model answer
Nitric acid is itself an oxidising agent, so it would oxidise some of the reducing agent being measured and give a titre that is too small.
- 6
State the ionic equation for the reaction of manganate(VII) with iron(II) ions in acid solution.
Model answer
The equation is MnO₄⁻ + 5Fe²⁺ + 8H⁺ → Mn²⁺ + 5Fe³⁺ + 4H₂O.
What is inside Levo
Six ways to work the same material.
Developing Metals revision questions
- What does Developing Metals cover in OCR A-Level Chemistry B?
- 18 subtopics: manganate(vii) titrations and their calculations, thiosulfate titrations, recording results and good technique, shapes of complexes and coordination number, balancing redox equations involving acid-base reactions, simple electrochemical cells, action of an electrochemical cell, standard electrode potentials and calculating e°cell, rusting and how it is prevented, transition metals: definition, oxidation states and colours, d-block electron configurations of the atoms and their ions, why transition metals show variable oxidation states, ligands and complex ions, coordinate bonding and what makes a ligand, bidentate and multidentate ligands, and finding a complex's formula, reactions of fe2+, fe3+ and cu2+ with hydroxide and ammonia, catalytic activity of transition metals, origin of colour in transition metal complexes and colorimetry. Each one has its own page with questions and model answers.
- How is Developing Metals organised?
- By the OCR H433 specification, subtopic by subtopic, so it matches the order you are taught it in.
Every question in Developing Metals, on a schedule.
Attempt a question from memory, write the correct version, then attempt it again. Levo records the jump between your first attempt and your last, and brings each question back on the day you are due to forget it.
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