4.2 Bonding, structure, and the properties of matter — coverage pack

18 specification leaves · notes, questions, answers and worked methods

4.2.1.1 · Chemical bonds

  • The three types of strong chemical bond are ionic, covalent and metallic: ionic bonding acts between oppositely charged ions, covalent bonding uses shared pairs of electrons, and metallic bonding involves delocalised electrons.
  • Use the elements present to choose a likely bonding type: metal with non-metal is usually ionic, non-metal with non-metal is covalent, and a metal element or alloy is metallic.
  • For example, sodium chloride forms by electron transfer, chlorine molecules contain shared electron pairs, and copper contains delocalised outer-shell electrons.
  • A common error is to name transferred or shared electrons without stating the electrostatic attraction that makes the bond strong.

Tier 1 · Easy

  1. 1. State the type of strong chemical bonding in sodium chloride, oxygen and copper.[3 marks]

    Answer

    • Sodium chloride: ionic bonding.
    • Oxygen: covalent bonding.
    • Copper: metallic bonding.

    Method: Sodium is a metal and chlorine is a non-metal, so sodium chloride is ionic. Oxygen is a non-metallic element whose atoms share electrons, so it is covalent. Copper is a metallic element, so it has metallic bonding.

Tier 2 · Standard

  1. 1. Magnesium reacts with chlorine to form magnesium chloride. Hydrogen atoms join to form hydrogen molecules. Compare how the strong bonds form in these two substances.[4 marks]

    Answer

    • In magnesium chloride, electrons are transferred from magnesium atoms to chlorine atoms.
    • The resulting oppositely charged ions attract electrostatically, forming ionic bonds.
    • In hydrogen, two atoms share a pair of electrons.
    • The shared pair is attracted to both nuclei, forming a covalent bond.

    Method: Treat each substance separately. Magnesium is a metal and chlorine is a non-metal, so describe electron transfer and attraction between the ions formed. Hydrogen contains only non-metal atoms, so describe a shared pair of electrons and its attraction to both nuclei.

Tier 3 · Hard

  1. 1. Substance P is a giant structure containing positive and negative particles. Substance Q is a giant structure containing one type of atom and mobile outer-shell electrons. Substance R contains separate groups of non-metal atoms joined by shared electron pairs. Identify the bonding in P, Q and R and explain the electrostatic attraction in each bond.[6 marks]

    Answer

    • P has ionic bonding: oppositely charged ions attract.
    • Q has metallic bonding: positive metal ions are attracted to delocalised electrons.
    • R has covalent bonding: each shared electron pair is attracted to the nuclei of the bonded atoms.

    Method: Match each particle description to a bonding model. Oppositely charged ions indicate ionic bonding. Mobile delocalised electrons in a giant metal structure indicate metallic bonding. Shared electron pairs between non-metal atoms indicate covalent bonding. Then state the relevant electrostatic attraction rather than stopping at the bond name.

4.2.1.2 · Ionic bonding

  • Ionic bonding begins when metal atoms lose outer-shell electrons to form positive ions and non-metal atoms gain those electrons to form negative ions.
  • For Groups 1 and 2, the positive ion charge matches the group number; Group 6 and 7 atoms form ions with charges 22- and 11- respectively.
  • For example, one calcium atom transfers one electron to each of two fluorine atoms, producing Ca<sup>2+</sup> and two F<sup>−</sup> ions in CaF<sub>2</sub>.
  • In a dot-and-cross diagram, show only outer-shell electrons, use different symbols for their origins, and put each ion in brackets with its charge.

Tier 1 · Easy

  1. 1. State the ions formed when potassium, a Group 1 metal, reacts with sulfur, a Group 6 non-metal.[2 marks]

    Answer

    • K<sup>+</sup>
    • S<sup>2−</sup>

    Method: A Group 1 atom loses one electron, so potassium forms K<sup>+</sup>. A Group 6 atom gains two electrons to complete its outer shell, so sulfur forms S<sup>2−</sup>.

Tier 2 · Standard

  1. 1. Describe the electron transfer when magnesium chloride, MgCl<sub>2</sub>, forms, and state the charge on every ion produced from one magnesium atom.[4 marks]

    Answer

    • The magnesium atom loses two outer-shell electrons.
    • Each of two chlorine atoms gains one electron.
    • One Mg<sup>2+</sup> ion and two Cl<sup>−</sup> ions form.

    Method: Magnesium is in Group 2, so it loses two electrons and forms Mg<sup>2+</sup>. Chlorine is in Group 7, so each atom gains one electron and forms Cl<sup>−</sup>. Two chlorine atoms are therefore needed to receive the two transferred electrons.

Tier 3 · Hard

  1. 1. Element X is in Group 2 and element Y is in Group 7. Describe a dot-and-cross diagram for the ionic compound they form and deduce its formula using X and Y.[5 marks]

    Answer

    • X loses two electrons to form X<sup>2+</sup>.
    • Two Y atoms each gain one electron to form two Y<sup>−</sup> ions.
    • Each ion is shown in brackets with a complete outer shell and its charge.
    • Dots and crosses distinguish electrons originally from X and Y, including the transferred electrons.
    • The formula is XY<sub>2</sub>.

    Method: Use the group numbers to obtain X<sup>2+</sup> and Y<sup>−</sup>. One X atom supplies two electrons, so two Y atoms are needed. In the diagram, use dots and crosses to distinguish the original and transferred outer-shell electrons, bracket every ion, and label the charges. The 1:21:2 ion ratio gives XY<sub>2</sub>.

4.2.1.3 · Ionic compounds

  • An ionic compound is a giant lattice of positive and negative ions held by strong electrostatic attractions acting in all directions.
  • To find an empirical formula from a model, count each type of ion and simplify the ratio to the smallest whole numbers.
  • For example, a model containing 1212 X<sup>2+</sup> ions and 2424 Y<sup>−</sup> ions has the ratio 1:21:2, so its empirical formula is XY<sub>2</sub>.
  • Dot-and-cross and ball-and-stick models are not literal pictures: they can misrepresent ion size, spacing, scale, bond direction and the full extent of the lattice.

Tier 1 · Easy

  1. 1. Describe the structure and bonding in a solid ionic compound.[2 marks]

    Answer

    • It has a giant lattice of oppositely charged ions.
    • Strong electrostatic attractions act between the ions in all directions.

    Method: Name both the scale of the structure and the force holding it together: a giant lattice, not separate molecules, with electrostatic attraction between opposite charges in every direction.

Tier 2 · Standard

  1. 1. A model of an ionic lattice contains 1818 M<sup>2+</sup> ions and 3636 N<sup>−</sup> ions. Work out the empirical formula of the compound.[2 marks]

    Answer

    • MN<sub>2</sub>

    Method: The ion count ratio is 18:3618:36. Divide both numbers by 1818 to obtain 1:21:2, so the simplest empirical formula is MN<sub>2</sub>. The charges also balance: one 2+2+ ion is matched by two 11- ions.

Tier 3 · Hard

  1. 1. A section of an ionic model contains 88 A<sup>3+</sup> ions and 1212 B<sup>2−</sup> ions. Deduce the empirical formula and give two limitations of using a ball-and-stick model for this lattice.[4 marks]

    Answer

    • The ion ratio 8:128:12 simplifies to 2:32:3.
    • The empirical formula is A<sub>2</sub>B<sub>3</sub>.
    • The model may not show the ions at their relative sizes or separations.
    • Sticks can suggest directional physical bonds that are not present.

    Method: Simplify the count ratio 8:128:12 by dividing by 44, giving 2:32:3 and hence A<sub>2</sub>B<sub>3</sub>. The charges balance because two A<sup>3+</sup> ions give +6+6 and three B<sup>2−</sup> ions give 6-6. For limitations, compare the simplified representation with a giant lattice whose electrostatic attractions act in all directions.

4.2.1.4 · Covalent bonding

  • A covalent bond is a shared pair of electrons between atoms, and the bond itself is strong.
  • Recognise whether a diagram represents a small molecule, a long polymer chain or part of a giant covalent structure before interpreting its formula or bonds.
  • For example, methane has one carbon atom sharing one electron pair with each of four hydrogen atoms, giving CH<sub>4</sub>.
  • A line represents one covalent bond, not a physical stick; a small drawn portion may also hide the much larger extent of a polymer or giant structure.

Tier 1 · Easy

  1. 1. A chlorine molecule contains two chlorine atoms joined by one covalent bond. State what this bond represents.[1 mark]

    Answer

    • A shared pair of electrons.

    Method: Use the definition of a covalent bond: the single bond between the two non-metal atoms represents one pair of electrons shared by both atoms.

Tier 2 · Standard

  1. 1. Describe a dot-and-cross diagram for one water molecule, H<sub>2</sub>O. Include the bonding pairs and the unshared outer-shell electrons on oxygen.[4 marks]

    Answer

    • Oxygen is in the centre with one hydrogen on each side.
    • There is one shared electron pair between oxygen and each hydrogen.
    • Oxygen also has two unshared pairs of outer-shell electrons.
    • Dots and crosses distinguish which atom supplied each electron.

    Method: Oxygen has six outer-shell electrons and each hydrogen has one. Oxygen shares one electron with each hydrogen, making two O–H shared pairs. Four oxygen electrons remain as two lone pairs. Use different symbols for electrons from oxygen and hydrogen.

Tier 3 · Hard

  1. 1. A model shows two nitrogen atoms joined together, with each nitrogen also joined to two hydrogen atoms. Deduce the molecular formula, count the covalent bonds shown, and give one limitation of the model.[3 marks]

    Answer

    • The molecular formula is N<sub>2</sub>H<sub>4</sub>.
    • Five covalent bonds are shown.
    • The sticks do not show electron pairs, or the model may not show realistic atom sizes, distances or bond angles.

    Method: Count atoms rather than bonds to obtain two nitrogen atoms and four hydrogen atoms, so the formula is N<sub>2</sub>H<sub>4</sub>. Count the one N–N connection and four N–H connections to obtain five bonds. A ball-and-stick model simplifies electron density, scale and geometry.

4.2.1.5 · Metallic bonding

  • Metals have giant structures in which atoms are arranged in a regular pattern and outer-shell electrons are delocalised throughout the structure.
  • When interpreting a metallic-bonding diagram, identify the regular positive metal ions and the delocalised electrons that can move through the whole lattice.
  • For example, a metallic-bonding model explains strength by the electrostatic attraction between each positive metal ion and the sea of negatively charged delocalised electrons throughout the lattice.
  • Do not describe a metal as separate molecules or say that its electrons belong to one neighbouring pair of atoms; the electrons are shared across the giant structure.

Tier 1 · Easy

  1. 1. Name the two types of charged particle shown in the usual model of metallic bonding.[2 marks]

    Answer

    • Positive metal ions.
    • Delocalised electrons.

    Method: The outer-shell electrons are no longer attached to individual atoms. The model therefore shows a regular array of positive metal ions surrounded by mobile, negatively charged delocalised electrons.

Tier 2 · Standard

  1. 1. Explain why the bonding in a metal is strong.[3 marks]

    Answer

    • Metal ions are positively charged.
    • Delocalised electrons are negatively charged.
    • There is a strong electrostatic attraction between the ions and delocalised electrons throughout the giant structure.

    Method: Identify the opposite charges and then state their attraction. Because the ions and delocalised electrons extend through a giant structure, the electrostatic attraction acts throughout the metal.

Tier 3 · Hard

  1. 1. A diagram shows identical circles in regular layers with many smaller negative symbols between them. A student says the diagram represents a simple molecule with electrons shared only between neighbouring pairs of atoms. Evaluate the student's statement.[5 marks]

    Answer

    • The diagram represents a giant metallic structure, not a simple molecule.
    • The circles represent positive metal ions in a regular arrangement.
    • The negative symbols represent delocalised electrons.
    • The electrons move through and are shared across the whole structure, not only one neighbouring pair.
    • Metallic bonding is the electrostatic attraction between the positive ions and delocalised electrons.

    Method: Use every feature of the diagram: regular repeated particles show a giant lattice, while many small negative symbols between them show delocalised electrons. Correct both parts of the claim, then give the electrostatic definition of metallic bonding.

4.2.2.1 · The three states of matter

  • Solids, liquids and gases differ in particle arrangement and movement; melting, freezing, boiling and condensing are physical changes between these states.
  • To predict state, compare the temperature with the melting point and boiling point: below melting is solid, between them is liquid, and above boiling is gas.
  • For example, a substance with melting point 20C-20\,^{\circ}\text{C} and boiling point 70C70\,^{\circ}\text{C} is liquid at 25C25\,^{\circ}\text{C}.
  • Melting and boiling require energy to overcome forces between particles, whereas freezing and condensing transfer energy to the surroundings; individual particles do not themselves melt or boil. Higher tier only: the simple model omits forces and represents every particle as a solid, inelastic sphere.

Tier 1 · Easy

  1. 1. At the boiling point, name the change from liquid to gas and the reverse change from gas to liquid.[2 marks]

    Answer

    • Liquid to gas: boiling.
    • Gas to liquid: condensing.

    Method: Use the named changes at the boiling point: heating a liquid produces a gas by boiling, while cooling a gas produces a liquid by condensing.

Tier 2 · Standard

  1. 1. Substance S has a melting point of 15C-15\,^{\circ}\text{C} and a boiling point of 84C84\,^{\circ}\text{C}. State its physical state at 30C-30\,^{\circ}\text{C}, 20C20\,^{\circ}\text{C} and 100C100\,^{\circ}\text{C}.[3 marks]

    Answer

    • At 30C-30\,^{\circ}\text{C}: solid.
    • At 20C20\,^{\circ}\text{C}: liquid.
    • At 100C100\,^{\circ}\text{C}: gas.

    Method: 30C-30\,^{\circ}\text{C} is below the melting point, so S is solid. 20C20\,^{\circ}\text{C} lies between the melting and boiling points, so S is liquid. 100C100\,^{\circ}\text{C} is above the boiling point, so S is a gas.

Tier 3 · Hard

  1. 1. Substance P melts at 40C40\,^{\circ}\text{C} and boils at 85C85\,^{\circ}\text{C}. Substance Q melts at 780C780\,^{\circ}\text{C} and boils at 1400C1400\,^{\circ}\text{C}. Compare their states at 100C100\,^{\circ}\text{C} and explain what the data suggest about the forces or bonds between their particles.[5 marks]

    Answer

    • P is a gas at 100C100\,^{\circ}\text{C}.
    • Q is a solid at 100C100\,^{\circ}\text{C}.
    • Q has much stronger forces or bonds between its particles than P.
    • More energy is needed to overcome the attractions in Q, giving it higher melting and boiling points.

    Method: 100C100\,^{\circ}\text{C} is above P's boiling point, so P is a gas, but it is below Q's melting point, so Q is solid. Higher change-of-state temperatures mean that more energy must be transferred to separate or rearrange the particles, so the attractions in Q are stronger.

4.2.2.2 · State symbols

  • Chemical equations use (s) for solid, (l) for liquid, (g) for gas and (aq) for a substance dissolved in water.
  • Choose each state symbol from the conditions and information given, then place it immediately after the correct chemical formula.
  • For example, magnesium reacting with hydrochloric acid can be written Mg(s) + 2HCl(aq) → MgCl<sub>2</sub>(aq) + H<sub>2</sub>(g).
  • Aqueous does not mean liquid: NaCl(aq) is sodium chloride dissolved in water, whereas NaCl(l) is molten sodium chloride.

Tier 1 · Easy

  1. 1. State the meaning of the symbols (l) and (aq) in a chemical equation.[2 marks]

    Answer

    • (l) means liquid.
    • (aq) means dissolved in water.

    Method: Read each symbol as a physical state. The symbol (aq) is reserved for an aqueous solution, so it must not be treated as another symbol for a pure liquid.

Tier 2 · Standard

  1. 1. At room conditions, methane, oxygen and carbon dioxide are gases, while the water produced is liquid. Represent the complete combustion of methane by a balanced symbol equation with a state symbol after each formula.[3 marks]

    Answer

    • CH<sub>4</sub>(g) + 2O<sub>2</sub>(g) → CO<sub>2</sub>(g) + 2H<sub>2</sub>O(l).

    Method: Balance carbon and hydrogen first, then oxygen. Translate the stated physical state of each substance directly: methane, oxygen and carbon dioxide receive (g), while water receives (l). Coefficients do not change state symbols.

Tier 3 · Hard

  1. 1. A technician mixes solutions of barium chloride and sodium sulfate. The barium sulfate product is a solid precipitate, while sodium chloride stays dissolved. Give, in order, the state symbols for barium chloride, sodium sulfate, barium sulfate and sodium chloride.[4 marks]

    Answer

    • Barium chloride: (aq).
    • Sodium sulfate: (aq).
    • Barium sulfate: (s).
    • Sodium chloride: (aq).

    Method: Both named reactant solutions receive (aq). The barium sulfate is stated to be a solid precipitate, so it receives (s). Sodium chloride remains dissolved in water, so it receives (aq), not (l).

4.2.2.3 · Properties of ionic compounds

  • Ionic compounds contain strong electrostatic attractions in all directions through a regular giant lattice.
  • Explain high melting and boiling points by linking the many strong ionic bonds to the large energy transfer needed to overcome them.
  • For example, solid sodium chloride does not conduct because its ions are fixed, but molten NaCl conducts because its ions are free to move and carry charge.
  • Do not say that electrons move through an ionic compound or that every ionic compound conducts when solid.

Tier 1 · Easy

  1. 1. State whether an ionic compound usually conducts electricity when solid and when molten.[2 marks]

    Answer

    • Solid: does not conduct.
    • Molten: conducts.

    Method: In the solid, the ions are held in fixed lattice positions and cannot carry charge through the material. Melting frees the ions to move, so the liquid conducts.

Tier 2 · Standard

  1. 1. Explain why magnesium oxide has a high melting point.[3 marks]

    Answer

    • Magnesium oxide has a giant ionic lattice.
    • There are strong electrostatic attractions between oppositely charged ions in all directions.
    • A large amount of energy is needed to overcome the many strong ionic bonds.

    Method: Build the explanation from structure to bonding to energy: identify the giant lattice, state the attraction between opposite charges, then connect the many strong attractions to the large energy transfer required for melting.

Tier 3 · Hard

  1. 1. Compound T has a high melting point. It does not conduct electricity as a solid, but it conducts when molten and when dissolved in water. Explain all three observations and identify the likely structure of T.[6 marks]

    Answer

    • T has a giant ionic lattice.
    • Strong electrostatic attractions act between oppositely charged ions in all directions.
    • Much energy is needed to overcome these attractions, so the melting point is high.
    • In the solid, ions are fixed and cannot carry charge through the lattice.
    • When molten or dissolved, ions are free to move and carry charge.

    Method: The combined pattern is diagnostic of an ionic compound. Use the giant lattice and strong attractions to explain the melting point. Then compare mobility: ions are fixed in the solid but mobile in the melt and aqueous solution. Charge is carried by ions, not by delocalised electrons.

4.2.2.4 · Properties of small molecules

  • Substances made from small molecules are often gases or liquids with relatively low melting and boiling points because forces between molecules are weak.
  • When comparing molecular substances, a larger molecule generally has stronger intermolecular forces and therefore a higher melting or boiling point.
  • For example, boiling methane separates CH<sub>4</sub> molecules by overcoming intermolecular forces; the strong covalent bonds within each molecule remain intact.
  • Small molecular substances usually do not conduct electricity because their molecules have no overall charge; do not explain low boiling points by calling covalent bonds weak.

Tier 1 · Easy

  1. 1. Explain why a substance made of small molecules can have a low boiling point even though its covalent bonds are strong.[2 marks]

    Answer

    • Only weak intermolecular forces need to be overcome when it boils.
    • The strong covalent bonds within the molecules are not broken.

    Method: Separate the two scales of attraction. Covalent bonds hold atoms together inside each molecule, but boiling moves whole molecules apart by overcoming the much weaker forces between them.

Tier 2 · Standard

  1. 1. Molecule V is larger than molecule U. Both substances consist of small molecules. Predict which substance usually has the higher boiling point and explain your answer.[3 marks]

    Answer

    • V usually has the higher boiling point.
    • Larger molecules have stronger intermolecular forces.
    • More energy is needed to overcome these forces between V molecules.

    Method: Apply the specified trend: increasing molecular size strengthens the forces between molecules. Stronger intermolecular forces require a larger energy transfer to overcome, so the boiling point is higher.

Tier 3 · Hard

  1. 1. Substances A and B both contain neutral small molecules. A has relative molecular mass 3434 and boils at 22C22\,^{\circ}\text{C}; B has relative molecular mass 122122 and boils at 168C168\,^{\circ}\text{C}. Explain the difference in boiling point and predict whether either pure substance conducts electricity.[5 marks]

    Answer

    • B is made of larger molecules than A.
    • B therefore has stronger intermolecular forces.
    • More energy is needed to overcome the forces between B molecules, so B has the higher boiling point.
    • Neither pure substance conducts electricity because the molecules have no overall charge.

    Method: Use relative molecular mass as evidence that B has larger molecules. Link larger molecules to stronger intermolecular forces and hence a greater energy requirement for boiling. For conductivity, use the stated neutral molecular particles: there are no mobile charged particles in either pure substance.

4.2.2.5 · Polymers

  • Polymers have very large molecules in which atoms are joined to other atoms by strong covalent bonds.
  • To recognise a polymer structure, trace a long molecular chain with a bonding pattern that repeats; separate chains are separate molecules.
  • The intermolecular forces between polymer molecules are relatively strong, so these polymer substances are solids at room temperature.
  • A polymer is not automatically a giant covalent structure: melting overcomes forces between its molecules, not the strong covalent bonds along each chain.

Tier 1 · Easy

  1. 1. A substance consists of separate, very long carbon-based chains. Name this class of substance and state the type of bond joining atoms within each chain.[2 marks]

    Answer

    • Polymer.
    • Covalent bonds join the atoms within a chain.

    Method: Use the phrase ‘separate, very long chains’ to identify a polymer. Then distinguish the bonds inside a molecule from the forces between molecules: the atoms along each chain are linked by strong covalent bonds.

Tier 2 · Standard

  1. 1. A short-chain molecular substance is a liquid at 20C20\,^\circ\text{C}, whereas material P, made from long covalent chains, is solid. Explain why P is solid at this temperature.[3 marks]

    Answer

    • P has very large polymer molecules.
    • The intermolecular forces between its molecules are relatively strong.
    • At 20C20\,^\circ\text{C} there is insufficient energy to overcome these forces, so P remains solid.

    Method: Build a structure-to-property chain. Long covalent chains mean very large molecules; these have relatively strong intermolecular forces. Link that explicitly to the state: room-temperature energy does not overcome enough of those forces for the molecules to move past one another.

Tier 3 · Hard

  1. 1. Material R contains long covalent chains with no covalent bonds from one chain to another. Material S is one continuous covalent network. Identify the polymer and explain two structural differences between R and S.[4 marks]

    Answer

    • R is the polymer.
    • R consists of separate very large molecules or chains.
    • Forces between R's chains are intermolecular forces rather than covalent bonds.
    • S is a giant covalent structure in which covalent bonds connect atoms throughout one continuous network.

    Method: First decide whether the covalent bonding stops at the edge of a molecule. It does in R, leaving separate chains, so R is the polymer. In S the covalent bonds continue throughout the structure, so S is a giant covalent network rather than a collection of polymer molecules.

4.2.2.6 · Giant covalent structures

  • A giant covalent structure is a continuous network in which all atoms are linked to other atoms by strong covalent bonds.
  • To identify one from a diagram, check that the bonding pattern continues throughout the structure instead of ending at separate molecules.
  • Melting or boiling requires many strong covalent bonds to be overcome, so giant covalent substances are solids with very high melting points.
  • Do not explain a giant covalent melting point using intermolecular forces: examples such as diamond and silicon dioxide do not consist of small, separate molecules.

Tier 1 · Easy

  1. 1. A diagram shows atoms covalently bonded in a repeating network that extends in every direction. State the type of structure shown.[1 mark]

    Answer

    • A giant covalent structure.

    Method: Look for a network with no boundary around an individual molecule. Because the covalent bonding continues throughout the sample, the structure is giant covalent.

Tier 2 · Standard

  1. 1. Silicon dioxide is solid at 1500C1500\,^\circ\text{C}. Explain this observation using its structure and bonding.[3 marks]

    Answer

    • Silicon dioxide has a giant covalent structure.
    • There are many strong covalent bonds between its atoms.
    • A large amount of energy is needed to overcome these bonds, giving it a very high melting point.

    Method: Name the structure, identify the strong bonds that extend throughout it, and then link bond strength to energy. Since 1500C1500\,^\circ\text{C} is still below the melting point, the structure remains solid.

Tier 3 · Hard

  1. 1. Two covalent substances are heated. U melts at 84C84\,^\circ\text{C} and consists of separate molecules. V is still solid at 1700C1700\,^\circ\text{C} and has no separate molecules. Deduce the structure of V and explain the difference in melting behaviour.[4 marks]

    Answer

    • V has a giant covalent structure.
    • Strong covalent bonds extend throughout V's network.
    • Many strong covalent bonds must be overcome to melt V, requiring a large amount of energy.
    • Melting U only overcomes intermolecular forces between its separate molecules, so U melts at a much lower temperature.

    Method: Use ‘no separate molecules’ and the extreme temperature to infer a giant network for V. Compare what must be overcome: covalent bonds throughout V but only intermolecular forces between U's molecules. This accounts for the large difference in energy needed.

4.2.2.7 · Properties of metals and alloys

  • Metals have giant structures of atoms held together by strong metallic bonding, so most metals have high melting and boiling points.
  • To explain why a pure metal can be shaped, link its regularly arranged layers of atoms to their ability to slide over one another.
  • Alloying introduces atoms of different sizes, distorting the regular layers and making it harder for the layers to slide, so the alloy is harder.
  • A common error is to say that alloys are harder because they contain more bonds; the required explanation is the distortion that obstructs layer movement.

Tier 1 · Easy

  1. 1. Explain why a pure metal can be bent into shape.[2 marks]

    Answer

    • Its atoms are arranged in layers.
    • The layers can slide over one another when a force is applied.

    Method: Identify the relevant structural feature, which is the layered arrangement of atoms, and link movement of those layers to the observed change of shape.

Tier 2 · Standard

  1. 1. A manufacturer replaces pure metal M with an alloy containing a second element whose atoms have a different size. Explain why the alloy is harder than M.[3 marks]

    Answer

    • The different-sized atoms distort the regular layers in M's structure.
    • The distorted layers cannot slide over one another as easily.
    • More force is therefore needed to change the alloy's shape, so it is harder.

    Method: Follow the causal sequence demanded by AQA: different atom sizes, then distortion of the layers, then reduced sliding. Finish by connecting reduced sliding to increased hardness.

Tier 3 · Hard

  1. 1. Pure metal Q bends when a force of 18N18\,\text{N} is applied, but an alloy of Q needs 47N47\,\text{N}. Both have high melting points. Explain both observations in terms of structure and bonding.[5 marks]

    Answer

    • Both materials have giant metallic structures with strong metallic bonding.
    • A large amount of energy is needed to overcome the strong metallic bonding, so their melting points are high.
    • Pure Q has regular layers of atoms that can slide over one another.
    • Different-sized atoms in the alloy distort these layers, making sliding more difficult.
    • Therefore the alloy needs the larger force to bend it.

    Method: Treat the two properties separately. Explain melting using strong metallic bonding in a giant structure. Explain bending using layer movement: regular layers slide in pure Q, while different-sized alloy atoms distort the layers and oppose sliding, consistent with 47N>18N47\,\text{N}>18\,\text{N}.

4.2.2.8 · Metals as conductors

  • Metallic structures contain delocalised electrons that are not tied to one atom and can move through the structure.
  • For electrical conduction, identify the mobile delocalised electrons and state that they carry electrical charge through the metal.
  • For thermal conduction, energy is transferred rapidly through the structure by the delocalised electrons.
  • Do not credit the metal ions with moving through a solid wire: the ions stay in fixed positions while delocalised electrons move and transfer charge or energy.

Tier 1 · Easy

  1. 1. Name the particles that carry electrical charge through a metal wire.[1 mark]

    Answer

    • Delocalised electrons.

    Method: In a solid metal the positive ions do not travel along the wire. The mobile charge carriers are the delocalised electrons.

Tier 2 · Standard

  1. 1. A metal strip completes a circuit, but a solid polymer strip does not. Explain why the metal conducts electricity.[3 marks]

    Answer

    • The metal contains delocalised electrons.
    • These electrons are free to move through the metallic structure.
    • Their movement carries electrical charge through the strip.

    Method: State which charged particles are present, establish that they are mobile, and then connect their motion to charge transfer. The comparison does not require claiming that the polymer has mobile ions or electrons.

Tier 3 · Hard

  1. 1. Copper is used for both electrical wiring and the base of a saucepan. Explain how the same structural feature makes copper suitable for both uses.[4 marks]

    Answer

    • Copper contains delocalised electrons.
    • The delocalised electrons can move through the metallic structure.
    • They carry electrical charge through a wire.
    • They also transfer thermal energy rapidly through the saucepan base.

    Method: Identify the shared cause before treating the two uses. Mobile delocalised electrons account for both properties: charge transport explains electrical conduction, while energy transfer by those electrons explains thermal conduction.

4.2.3.1 · Diamond

  • Diamond is a giant covalent structure in which each carbon atom forms four covalent bonds with other carbon atoms.
  • To explain a diamond property, begin with its four-bonded rigid network and then identify whether bond strength or electron mobility controls the property.
  • The many strong covalent bonds make diamond very hard and give it a very high melting point.
  • A common error is to assume diamond conducts merely because it is carbon; all four outer electrons of each atom are used in bonds, so there are no delocalised electrons.

Tier 1 · Easy

  1. 1. In diamond, how many bonds per carbon?[1 mark]

    Answer

    • Four covalent bonds.

    Method: Recall that diamond uses all four outer electrons of each carbon atom to make four covalent bonds in its giant structure.

Tier 2 · Standard

  1. 1. Explain why a diamond-tipped cutting tool can scratch most materials.[3 marks]

    Answer

    • Diamond has a giant covalent structure.
    • Each carbon atom is joined by four strong covalent bonds in a rigid network.
    • A large force is needed to deform or break this network, so diamond is very hard.

    Method: Translate the use into the required property, hardness. Then link hardness to the rigid three-dimensional network of four strong covalent bonds around each carbon atom.

Tier 3 · Hard

  1. 1. Diamond is proposed for an electrically heated cutting element. Explain its high melting point and hardness, and decide whether it can carry the heating current.[5 marks]

    Answer

    • Diamond has a giant covalent structure with four covalent bonds from each carbon atom.
    • Many strong covalent bonds must be overcome to melt it, so its melting point is very high.
    • The rigid network of strong bonds makes diamond hard.
    • All four outer electrons of each carbon atom are used in covalent bonds, so there are no delocalised electrons.
    • Diamond cannot carry the heating current because it does not conduct electricity.

    Method: Separate the three requested properties. Use strong covalent bonds throughout the network for melting point, rigidity for hardness, and the absence of mobile delocalised electrons for electrical conduction. The last point rules out diamond as the current-carrying element.

4.2.3.2 · Graphite

  • In graphite, each carbon atom forms three covalent bonds, producing layers of hexagonal rings with no covalent bonds between the layers.
  • Choose the relevant feature for each property: strong covalent bonds within layers affect melting, while the lack of covalent bonds between layers allows sliding.
  • One electron from each carbon atom is delocalised and can carry charge, so graphite conducts electricity in a similar way to metals.
  • Do not say graphite is soft because its covalent bonds are weak; its layers slide because only weak forces, not covalent bonds, act between them.

Tier 1 · Easy

  1. 1. State the number of covalent bonds made by each carbon atom in graphite.[1 mark]

    Answer

    • Three covalent bonds.

    Method: Each graphite carbon bonds to three neighbouring carbon atoms in a hexagonal layer, leaving one electron delocalised.

Tier 2 · Standard

  1. 1. Explain why graphite can be used as an electrode.[3 marks]

    Answer

    • One electron from each carbon atom is delocalised.
    • The delocalised electrons can move through the structure.
    • They carry electrical charge, so graphite conducts electricity.

    Method: An electrode must conduct. Identify the delocalised electron supplied by each carbon atom, state that these electrons are mobile, and connect their movement to charge transfer.

Tier 3 · Hard

  1. 1. Graphite is used in a high-temperature electrical contact that must also slide against another surface. Explain three properties that make graphite suitable.[6 marks]

    Answer

    • Graphite has strong covalent bonds between carbon atoms within each layer.
    • Many strong bonds require a large amount of energy to overcome, so graphite has a high melting point.
    • One electron per carbon atom is delocalised.
    • The delocalised electrons move and carry charge, so graphite conducts electricity.
    • There are no covalent bonds between adjacent layers, only weak forces.
    • The layers can slide over one another, so the contact can move with low friction.

    Method: Match one structural feature to each demand. Strong bonds within layers give thermal stability; delocalised electrons give electrical conduction; the absence of covalent bonds between layers allows them to slide. Keep the within-layer and between-layer bonding explanations distinct.

4.2.3.3 · Graphene and fullerenes

  • Graphene is a single layer of graphite: a one-atom-thick sheet of hexagonally arranged carbon atoms with delocalised electrons.
  • Relate graphene's strong covalent bonds, electrical conductivity and very small thickness to uses in composites and electronics.
  • Fullerenes are hollow carbon molecules based mainly on hexagonal rings, sometimes with five- or seven-membered rings; Buckminsterfullerene, C<sub>60</sub>, is spherical.
  • Do not confuse carbon nanotubes with solid rods: they are cylindrical fullerenes with very high length-to-diameter ratios and uses in nanotechnology, electronics and materials.

Tier 1 · Easy

  1. 1. Describe the relationship between graphene and graphite.[1 mark]

    Answer

    • Graphene is a single layer of graphite.

    Method: Treat graphite as a stack of carbon layers. One isolated layer from that stack is graphene.

Tier 2 · Standard

  1. 1. An electronic sensor needs a conducting layer that adds very little thickness. Explain why graphene is suitable.[4 marks]

    Answer

    • Graphene is a single layer of graphite and is only one atom thick.
    • It therefore adds very little thickness to the sensor.
    • Graphene contains delocalised electrons.
    • The electrons can move and carry charge, so graphene conducts electricity.

    Method: Extract the two design requirements: small thickness and electrical conduction. Link the first to graphene being a single atomic layer, and the second to its mobile delocalised electrons.

Tier 3 · Hard

  1. 1. Three carbon materials are described: A is a one-atom-thick sheet; B is a hollow sphere containing 60 carbon atoms; C is a hollow cylinder whose length is far greater than its diameter. Identify A, B and C, then give one suitable type of application for A and one for C.[5 marks]

    Answer

    • A is graphene.
    • B is Buckminsterfullerene or C<sub>60</sub>.
    • C is a carbon nanotube.
    • A is suitable for electronics or as part of a composite.
    • C is suitable for nanotechnology, electronics or materials.

    Method: Use the defining shapes first: one layer identifies graphene, the 60-atom hollow sphere identifies Buckminsterfullerene, and the high-aspect-ratio cylinder identifies a nanotube. Then select applications from the specified families rather than inventing a shape-dependent use that has not been supported.

4.2.4.1 · Sizes of particles and their properties (chemistry only)

  • Nanoscience concerns structures from 11 to 100nm100\,\text{nm}, of the order of a few hundred atoms; fine particles span 100100 to 2500nm2500\,\text{nm} and coarse particles span 25002500 to 10000nm10\,000\,\text{nm}.
  • For a cube of side aa, calculate surface area as 6a26a^2 and volume as a3a^3, then simplify the surface-area-to-volume ratio; it equals 6/a6/a.
  • Reducing a cube's side by a factor of 1010 increases its surface-area-to-volume ratio by a factor of 1010, so nanoparticles can behave differently from the bulk material.
  • A common error is to compare surface areas alone: particle effects depend on surface area relative to volume, and a higher ratio can make a smaller quantity effective.

Tier 1 · Easy

  1. 1. Particle T is 72nm72\,\text{nm} across. A typical atom is 0.24nm0.24\,\text{nm} across. State whether T is nano, fine or coarse, and calculate how many atom diameters span T.[2 marks]

    Answer

    • T is a nanoparticle.
    • 300300 atom diameters span T.

    Method: The size 72nm72\,\text{nm} lies inside the nano interval 11100nm100\,\text{nm}. Because both dimensions use nanometres, compare them directly: 72/0.24=30072/0.24=300, so T spans about 300300 atom diameters.

Tier 2 · Standard

  1. 1. A nano-cube has edge length 5nm5\,\text{nm}. Calculate its surface area, volume and surface-area-to-volume ratio.[3 marks]

    Answer

    • Surface area =150nm2=150\,\text{nm}^2.
    • Volume =125nm3=125\,\text{nm}^3.
    • Surface-area-to-volume ratio =1.2:1=1.2:1.

    Method: A cube has six square faces, so A=6a2=6×52=150nm2A=6a^2=6\times5^2=150\,\text{nm}^2. Its volume is V=a3=53=125nm3V=a^3=5^3=125\,\text{nm}^3. Therefore A:V=150:125=1.2:1A:V=150:125=1.2:1.

Tier 3 · Hard

  1. 1. Fine particles have side 800nm800\,\text{nm}; nano-sized cubes of the same material have side 40nm40\,\text{nm}. Determine how many times larger the nano cubes' surface-area-to-volume ratio is. If effectiveness per gram is proportional to this ratio and 12g12\,\text{g} of the fine particles is effective, estimate the effective mass of nano cubes.[4 marks]

    Answer

    • The nano cubes' surface-area-to-volume ratio is 2020 times larger.
    • Estimated nano mass =0.60g=0.60\,\text{g}.

    Method: For similar cubes, A:V=6/aA:V=6/a, so the ratio increases by the inverse side-length factor: 800/40=20800/40=20. Under the stated proportional-effectiveness assumption, divide the required mass by 2020: 12/20=0.60g12/20=0.60\,\text{g}.

4.2.4.2 · Uses of nanoparticles (chemistry only)

  • Nanoparticles are used in medicine, electronics, cosmetics and sun creams, deodorants and catalysts, with new applications still being researched.
  • To evaluate a proposed use, compare relevant benefits, such as a smaller effective quantity or useful surface behaviour, with evidence about cost, performance and risk.
  • For example, a nanoparticulate catalyst can expose a large surface area using little material, potentially reducing resource use while maintaining reaction performance.
  • Do not claim that nanoparticles are proven safe or harmful without evidence: their possible health and environmental risks must be considered because their small size may change how they interact with organisms.

Tier 1 · Easy

  1. 1. Give two application areas in which nanoparticles are used.[2 marks]

    Answer

    • Any two from medicine, electronics, cosmetics, sun creams, deodorants and catalysts.

    Method: Select two distinct application areas from the specification list. Do not give two products from the same area if the question asks for two areas.

Tier 2 · Standard

  1. 1. A catalyst works equally well when a factory replaces 8.0g8.0\,\text{g} of bulk material with 0.40g0.40\,\text{g} of nanoparticles. Suggest two advantages and one possible disadvantage of the change.[4 marks]

    Answer

    • The nanoparticles have a high surface-area-to-volume ratio, so less catalyst is needed for the same effect.
    • Using less material may reduce raw-material use or cost.
    • Less catalyst may also reduce waste or the mass that must be handled.
    • A possible disadvantage is uncertain health or environmental risk if nanoparticles enter organisms or the environment.

    Method: Use the supplied equal-performance data to justify the benefits rather than assuming better performance. Credit the smaller mass through its high surface-area-to-volume ratio, then state a resource, cost or waste advantage. Balance this with a possible risk caused by the particles' small size.

Tier 3 · Hard

  1. 1. A company compares two sun creams. Product J uses larger particles, blocks 96%96\% of ultraviolet radiation and leaves a visible layer. Product K uses nanoparticles, blocks 94%94\%, is transparent and needs one quarter as much active material. Tests detect K's particles inside 2%2\% of sampled skin cells, but no harm has been established. Evaluate which product the company should develop.[6 marks]

    Answer

    • J blocks slightly more ultraviolet radiation: 96%96\% compared with 94%94\%.
    • K is transparent, which may make it more acceptable to users.
    • K needs only one quarter as much active material, so it may reduce resource use, cost or waste.
    • Detection inside some cells shows exposure is possible and creates a potential health concern.
    • The data do not show that K causes harm, so the risk remains uncertain rather than proven.
    • A justified conclusion may choose either product, but should weigh performance and user/resource benefits against the uncertainty and recommend further safety testing before K is widely used.

    Method: Compare every relevant datum: protection, appearance, quantity required and cell exposure. Distinguish evidence of entry into cells from evidence of harm. Reach a conditional judgement; for example, K has strong practical and resource advantages, but development should include further safety testing because the long-term risk is unresolved.