Edexcel A-Level Chemistry Paper 2, June 2025: Question 2
8 marks · Medium difficulty · Open Response
Explain differences in physical properties and boiling temperatures based on intermolecular forces, molecular shapes, and dipole moments.
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How to answer it
Intermolecular Forces & Physical Properties
This question assesses your understanding of the relationship between molecular structure, intermolecular forces, and physical properties (boiling temperature and volatility):
- Effect of branching on London forces: How surface contact area changes boiling temperature among structural isomers.
- Comparing intermolecular forces: Contrasting hydrogen bonding with London forces in molecules of equal electron number.
- Phase changes in simple molecular solids: Identifying the intermolecular forces broken during physical state transitions.
- Molecular geometry and overall polarity: Predicting shapes using VSEPR, evaluating bond dipole cancellation, and linking permanent dipole–dipole forces to boiling temperatures.
Boiling Temperatures of Alkane Isomers (C₈H₁₈)
Identifying the isomer with the lowest boiling point
✅ Correct Answer
A — (CH₃)₂CHCH₂C(CH₃)₃ (2,2,4-trimethylpentane)
💡 Key Knowledge
- All isomers of octane (C₈H₁₈) have the same molecular mass and identical number of electrons (66 electrons).
- Branching reduces the surface area of contact between adjacent molecules.
- Fewer points of contact mean weaker London dispersion forces, which need less thermal energy to overcome, resulting in a lower boiling point.
- Option A has three methyl branches (most branched), while B and C have only two, and D has none.
❌ Common Errors
Selecting D (octane). Students often confuse lowest boiling temperature with highest. Unbranched straight-chain alkanes pack closely and have the highest surface contact area, giving them the highest boiling temperature.
🧠 Exam Technique
Always circle key words like lowest or highest. Quickly count the number of branches in condensed structural formulas: A has 3 branches, B has 2, C has 2, D has 0.
Volatility: Pentan-1-ol vs Hexane
Explaining why equielectronic molecules differ in volatility
✅ Model Answer & Mark Scheme
- M1: (Only) pentan-1-ol has hydrogen bonds (between molecules), whereas hexane only has London dispersion forces.
- M2: Intermolecular forces in pentan-1-ol are stronger and require more energy to overcome / break (hence it is less volatile).
• Reverse argument is fully acceptable: Hexane only has London forces which are weaker than hydrogen bonds, requiring less energy to break.
• Do NOT award marks if covalent bonds are mentioned as breaking.
💡 Key Knowledge
- Pentan-1-ol (C₅H₁₁OH) and hexane (C₆H₁₄) both have 50 electrons, meaning their London dispersion forces are comparable in magnitude.
- Pentan-1-ol has a highly electronegative O atom bonded to H, allowing intermolecular hydrogen bonding.
- Volatility is the tendency of a substance to vaporise. Stronger intermolecular forces = higher boiling point = lower volatility.
❌ Common Misconceptions
- "Covalent O–H bonds break when boiling": A fatal error! Covalent bonds remain completely intact; only intermolecular forces are overcome.
- Vagueness: Saying "pentan-1-ol has hydrogen bonds so it takes more energy" without explicitly comparing strength or stating that hydrogen bonds are stronger than the London forces in hexane.
🧠 Exam Technique
Structure comparison questions in two sentences:
- Name the specific intermolecular force present in each compound.
- Compare their relative strengths and explicitly link to the energy required to overcome them.
Sublimation / Vaporisation of Iodine
Forces overcome during physical phase changes of molecular elements
✅ Correct Answer
C — London forces
💡 Key Knowledge
- Iodine exists as simple diatomic molecules: I₂ .
- In solid iodine, I₂ molecules are held in a regular crystal lattice by London dispersion forces (induced dipole–dipole forces).
- Upon heating, these weak intermolecular forces break, allowing molecules to separate into the gas phase. The covalent I–I bonds do not break.
❌ Common Distractors
- A (Covalent bonds): Only broken during chemical reactions or in giant covalent lattices (like diamond or graphite), never during simple molecular boiling/sublimation.
- D (Permanent dipole–dipole): Homonuclear diatomic molecules like I₂ have identical electronegativities, so the bond is non-polar and has no permanent dipole.
Boiling Points of BCl₃ vs PCl₃
Linking 3D molecular shape, dipole cancellation, and physical properties
📐 4-Step Structural Marking Breakdown
To score all 4 marks, your answer must connect four sequential logical steps:
- Shape of BCl₃: Boron trichloride has a trigonal planar shape.
- Shape of PCl₃: Phosphorus trichloride has a (trigonal) pyramidal shape.
- Dipole Cancellation & Polarity: In BCl₃, the bond dipoles are symmetrical and cancel out (no overall dipole moment), whereas in PCl₃ the dipoles do not cancel / it is a polar molecule (has an overall permanent dipole).
- Intermolecular Force & Energy: Therefore, PCl₃ has permanent dipole–dipole forces between molecules (requiring more energy to break, resulting in a higher boiling temperature).
✅ Model Answer
"Boron trichloride has 3 bonding pairs and no lone pairs around B, giving it a trigonal planar shape. Phosphorus trichloride has 3 bonding pairs and 1 lone pair around P, giving it a pyramidal shape.
Due to its symmetrical planar shape, the bond dipoles in BCl₃ cancel out, making it non-polar. In PCl₃, the asymmetrical pyramidal geometry means the dipoles do not cancel, giving the molecule an overall permanent dipole.
Consequently, PCl₃ molecules are held together by permanent dipole–dipole forces (in addition to London forces), which require more energy to break than the forces in BCl₃, giving PCl₃ a much higher boiling temperature."
• M1: Trigonal planar shape of BCl₃
• M2: Pyramidal shape of PCl₃
• M3: Dipoles cancel in BCl₃ / BCl₃ non-polar AND PCl₃ has overall dipole
• M4: Permanent dipole–dipole forces in PCl₃ explained
💡 VSEPR Theory Refresher
| Feature | BCl₃ | PCl₃ |
|---|---|---|
| Outer electrons of central atom | 3 (Boron) | 5 (Phosphorus) |
| Bond pairs / Lone pairs | 3 BP, 0 LP | 3 BP, 1 LP |
| Shape name | Trigonal planar (120°) | Pyramidal (107°) |
| Symmetry & Net dipole | Symmetrical; Dipoles cancel; μ = 0 | Non-symmetrical; Dipoles reinforce; μ > 0 |
❌ Examiner Pitfalls & Lost Marks
- Saying "charges cancel": The mark scheme explicitly states "Do not award: the charges cancel". You must say dipoles cancel or dipole vectors cancel.
- Discussing London forces: The question explicitly says "Do not consider differences in London forces." Any time spent discussing electron count or London forces gains zero credit.
- Missing the lone pair effect: Describing PCl₃ as "planar" or "tetrahedral" instead of pyramidal.
- Stopping short: Stating that PCl₃ is polar, but failing to name the intermolecular force: permanent dipole–dipole forces.
🧠 Diagram Advice (If Drawing)
If you choose to draw 3D diagrams instead of writing descriptions:
- BCl₃: Draw a flat planar structure with 120° bond angles and dipoles pointing towards Cl (δ+ on B, δ− on each Cl).
- PCl₃: Must use wedge-and-dash bonds to show 3D tetrahedral/pyramidal geometry, show the lone pair on P, and draw a clear net dipole arrow pointing downwards.
Topics
Physical Chemistry · Topic 2: Bonding and Structure
Question and mark scheme from the Edexcel A-Level Chemistry examination, Paper 2, June 2025. QuestionVault is an independent revision resource; questions remain the copyright of the awarding body.