Explain a physical property by naming the particles, the attraction and what must move or be overcome.
Metal ions and delocalised electrons
Metallic bonding is electrostatic attraction between positive metal ions and delocalised electrons. Mobile electrons conduct electricity in solid and molten metals; positive ions are not the mobile carriers in the solid. Layers can move while metallic attraction persists, allowing malleability.
From Na to Mg to Al, higher cation charge, more delocalised electrons per atom and smaller ions generally strengthen attraction, explaining the broad rise in melting point. Do not use this simple model to assert a perfectly smooth trend across all metals.
Networks of strong covalent bonds
These giant covalent networks are insoluble in ordinary solvents because dissolving would require disruption of strong covalent bonding throughout the structure. Metals do not dissolve as intact metal lattices in water; reactive metals instead undergo chemical reactions. Many metals and giant covalent solids have high boiling points, although individual metal melting points vary widely. Graphene’s combination of strength, thinness and conductivity makes it useful in research into composites, sensors and conducting films.
| Substance | Connectivity | Consequences |
|---|---|---|
| Diamond | Each C bonded to four in a tetrahedral 3D network | Very hard, high melting/sublimation temperature; no mobile electrons for conduction |
| Graphite | Each C bonded to three in hexagonal sheets; delocalised electrons within sheets | Conducts along sheets; weak attractions between sheets allow sliding |
| Graphene | One carbon sheet, each C bonded to three | Very strong in-plane, thin and electrically conducting |
| Silicon | Each Si bonded to four in a giant tetrahedral network | High melting point; semiconductor rather than a metal-like conductor |
Period 2 and Period 3 change structure
Period 2: Li and Be are metallic; B and C form giant covalent structures; N₂, O₂ and F₂ are simple molecules; Ne consists of single atoms. Breaking a giant covalent network takes much more energy than overcoming intermolecular attractions in small molecules.
Period 3: Na, Mg and Al are metallic; Si is giant covalent; P₄, S₈ and Cl₂ are molecular; Ar is monatomic. The sharp drop from Si to phosphorus follows a change from a giant network to molecules. Among these molecular elements, S₈ has more electrons and stronger London forces than P₄ or Cl₂, helping explain its higher melting point.
Diamond, graphite and graphene are forms of carbon, not different elements. Graphite’s softness is caused by layer sliding, while its high thermal resistance comes from strong covalent bonds within the layers. Do not call the layers individual simple molecules.
Explain a property using the particles that can move
First decide whether the solid is metallic, giant covalent or molecular. Then decide what the process requires. Melting a molecular solid mainly overcomes intermolecular attractions; it does not normally split the molecules into atoms. Melting a network requires disruption of strong covalent bonding. Electrical conduction instead requires mobile charged particles, so a high melting point alone does not establish conductivity.
In solid magnesium, delocalised electrons move through the structure under an applied potential difference. Magnesium ions vibrate about lattice positions; they do not migrate through the solid to carry the current. In a molten metal the electrons remain mobile. In a molecular solid such as sulfur, neutral molecules and localised bonding electrons do not supply comparable mobile carriers.
Why graphite is both soft and thermally resistant
Two different directions involve different interactions. Within each graphite sheet, every carbon makes three strong covalent bonds. Separating a sheet into individual atoms therefore takes much energy. Between sheets, much weaker attractions allow the layers to slide over one another, explaining softness and lubrication.
The remaining electron per carbon contributes to delocalisation within the sheet, providing mobile charge carriers. Do not locate the conducting electrons only in the gaps between layers. Graphene is one such sheet: it has no stack of layers to slide, even though it shares graphite’s in-plane bonding and delocalisation.
Worked evidence: identify a likely structure
An invented solid has a very high melting temperature, conducts electricity and can leave a soft mark on paper. High melting temperature suggests strong bonding throughout substantial parts of the solid. Conductivity requires mobile charge carriers. Softness rules out using “all giant covalent structures are hard” as a shortcut. Together, these observations are consistent with graphite’s strongly bonded conducting sheets and weak interlayer attractions.
Now compare a low-melting solid that does not conduct and forms discrete eight-atom molecules. A simple molecular model fits: weak attractions between molecules explain the low melting point. The number of atoms in a molecule does not turn it into a giant lattice.
| Evidence | What it supports | What it does not prove |
|---|---|---|
| Conducts as a solid | Mobile charge carriers | Every conducting solid is a metal |
| High melting temperature | Strong interactions must be overcome | The exact type of bonding |
| Low boiling temperature | Relatively weak attractions between particles | Weak covalent bonds inside a molecule |
Quick checks
Original Finesse questions. Reveal the indicative worked solutions after attempting each question; these are not official OCR A mark allocations.
Q1. What charge carrier moves in solid magnesium?Show answer
Delocalised electrons.
Q2. Why does diamond not conduct electricity under ordinary conditions?Show answer
Its valence electrons are localised in covalent bonds; there are no mobile charge carriers.
Q3. Why is graphite soft but difficult to melt?Show answer
Weak attractions between layers allow sliding, while many strong covalent bonds within layers require much energy to break.
Q4. Why does melting point drop sharply from Si to P₄?Show answer
Silicon has a giant covalent network; solid P₄ has molecules held by much weaker intermolecular forces.
Q5. What is graphene?Show answer
A single sheet of carbon atoms in a hexagonal network, each bonded to three neighbours with delocalised electrons.
Q6. A student says “sulfur melts by breaking its S–S bonds”. Improve the explanation.Show answer
Sulfur contains S₈ molecules. Melting mainly overcomes London attractions between those molecules; it does not normally break the covalent S–S bonds within each ring.
Q7. Explain why solid aluminium conducts but diamond does not.Show answer
Aluminium has delocalised electrons able to move and carry charge. In diamond, valence electrons are localised in its four covalent bonds per carbon, so there are no comparable mobile charge carriers.
Q8. Explain the difference between graphite’s softness and graphene’s in-plane strength.Show answer
Graphite layers can slide because attractions between layers are weak. Graphene is a single sheet with strong covalent bonds throughout the sheet, giving high in-plane strength. These concern different interactions and directions.
Q9. Give a connected explanation of the Si → P₄ melting-point drop and the higher melting point of S₈ than P₄.Show answer
Si has a giant covalent network; melting requires much energy to disrupt strong bonding. P₄ is molecular and melting overcomes weaker intermolecular forces.
S₈ molecules have more electrons and more polarisable clouds than P₄, producing stronger London attractions and requiring more energy to overcome them. Crystal structure also influences exact melting temperatures.
Sources
Sources and examiner guidance (reviewed 6 October 2026)
- OCR A H032 specification, version 2.0 — 3.1.1(a–g); AS outcomes and additional guidance. Content rechecked 6 October 2026 against the retrieved version 2.0 copy.
- Chemrevise — OCR A 3.1.1 periodicity — Pages 1–5; coverage reference. Explanations and questions on this page are original.
- OCR H032/01 mark scheme — June 2025 — Q21(c); printed pages 10. Read with the question paper.
- OCR H032/01 examiner report — June 2025 — Q21(c); printed pages 20. Question-specific assessment guidance.
- OCR H032/02 mark scheme — June 2025 — Q2(a)(i); printed pages 11. Read with the question paper.
- OCR H032/02 examiner report — June 2025 — Q2(a)(i); printed pages 8. Question-specific assessment guidance.
- OCR H032/01 question paper — June 2025 — Question context for the question numbers listed with the mark scheme and examiner report.
- OCR H032/02 question paper — June 2025 — Question context for the question numbers listed with the mark scheme and examiner report.
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