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.

Practise this question

Question

Question 2 consists of four parts regarding intermolecular forces. Part (a) is a 1-mark multiple-choice question asking which isomer of C8H18 has the lowest boiling temperature, with four condensed structural formula options (A to D). Part (b) asks to explain why pentan-1-ol is much less volatile than hexane despite having the same number of electrons (2 marks). Part (c) is a 1-mark multiple-choice question asking what bonds or forces are broken when solid iodine vaporises (options: covalent bonds, ionic bonds, London forces, permanent dipole-dipole forces). Part (d) provides boiling temperatures for boron trichloride (13 °C) and phosphorus trichloride (76 °C), asking students to explain the higher boiling point of phosphorus trichloride in terms of molecular shapes and polar bonds, ignoring differences in London forces (4 marks).

Mark scheme

Show the mark scheme The mark scheme is divided into four sections: 2(a) awards 1 mark for option A, explaining that it is the most branched isomer. 2(b) awards 2 marks: one for stating pentan-1-ol forms hydrogen bonds, and one for stating its intermolecular forces are stronger and require more energy to break. 2(c) awards 1 mark for option C (London forces). 2(d) awards 4 marks: Mark 1 for BCl3 being trigonal planar, Mark 2 for PCl3 being pyramidal, Mark 3 for explaining that dipoles cancel in BCl3 so it has no net dipole while PCl3 is polar, and Mark 4 for concluding that PCl3 has permanent dipole-dipole forces between molecules leading to a higher boiling temperature.

How to answer it

Intermolecular Forces & Physical Properties

📋 What this question tests

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.
Part (a) — 1 Mark

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)

1 Mark: Correct option identified.

💡 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.

Part (b) — 2 Marks

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).
Guidance:
• 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:

  1. Name the specific intermolecular force present in each compound.
  2. Compare their relative strengths and explicitly link to the energy required to overcome them.
Part (c) — 1 Mark

Sublimation / Vaporisation of Iodine

Forces overcome during physical phase changes of molecular elements

✅ Correct Answer

C — London forces

1 Mark: Option C correctly selected.

💡 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.
Part (d) — 4 Marks

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:

  1. Shape of BCl₃: Boron trichloride has a trigonal planar shape.
  2. Shape of PCl₃: Phosphorus trichloride has a (trigonal) pyramidal shape.
  3. 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).
  4. 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."

Marks awarded:
• 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.