Edexcel A-Level Chemistry Paper 3, June 2024: Question 2

8 marks · Medium difficulty · Short Open Response

Explain how London forces arise, determine which of four isomeric alkanes has the highest boiling temperature, and explain whether three given liquids with different polarities will be deflected by a charged rod.

Practise this question

Question

Exam question about intermolecular forces featuring skeletal structures of four isomeric alkanes (compounds A, B, C, D). Part (a) asks to explain how London forces arise. Part (b) asks to explain which compound has the highest boiling temperature. Part (c) includes a diagram of an apparatus with a burette releasing a stream of liquid past a charged rod into a beaker, followed by the structural formulas of CCl4, CHCl3, and C6H14, and asks to explain whether each liquid will be deflected.
Question text

2 This question is about the intermolecular forces in organic compounds.

The structures of four isomeric alkanes are shown.

compound A compound B compound C compound D

The only significant intermolecular forces between molecules of these compounds

are London forces.

(a) Explain how London forces arise.

(3)

(b) Explain which of the compounds A–D will have the highest boiling temperature.

(2)

(c) The apparatus shown may be used in an experiment to compare how far, if at all,

a charged rod deflects different liquids.

burette 3

*P74455A0332*

stream of liquid charged rod

+ + + + + + +

beaker

The structures of three liquids are shown.

H H H

Cl H H H H

H C C C

C C C C C H

Cl Cl Cl Cl H H H

Cl Cl H H H

CCl4 CHCl3 C6H14

Explain whether or not each of these liquids will be deflected in this experiment.

(3)

(Total for Question 2 = 8 marks)

Mark scheme

Show the mark scheme Mark scheme detailing points for 2(a) covering random electron movement, temporary dipoles, and induced dipoles in neighbouring molecules. For 2(b), points cover unbranched compound A having stronger London forces due to greater surface area/points of contact. For 2(c), a table and point criteria explain deflection based on molecular polarity and symmetry for CCl4, CHCl3, and C6H14.

Question

Answer Additional Guidance Mark

Number

2(a) An explanation that makes reference to the following points: Allow reference to atoms throughout but for (3)

M3 a second/different atoms should be clear

(Setting up of the dipole)

• (random) movement of electrons / Allow reference to electron density

(temporary) uneven distribution of electrons /

Fluctuation of electrons (1)

(Type of dipole)

• (this results in an) instantaneous/temporary dipole Allow oscillating dipole

(in the first molecule) (1) Do not award reference to permanent dipole

(Induction of a second dipole)

• (which) causes/induces a (second) dipole in a Allow in/on another molecule for adjacent

neighbouring/adjacent molecule (1) Do not award reference to permanent dipole

M3 is consequential on M2 or a near miss

Allow a labelled diagram for evidence of these

marks

Ignore any reference to attraction stated thereafter

Penalise reference to electronegativity once only

Question

Answer Additional Guidance Mark

Number

2(b) An answer that makes reference to the following points: (2)

• compound A as London forces increase as branching decreases Allow van der Waals’/dispersion forces/

or induced dipole – dipole forces for London forces

compound A is unbranched and has greater/more London forces (1) Allow ‘least branching’/ ‘longer chain’ for

unbranched

• so surface area/points of contact (of molecules) increases (1) Allow reference to packing of molecules more

closely/closer together

Allow compound for molecule

Ignore A molecules are more compact

Do not award ‘more electrons’

Do not award M2 if clear reference to covalent

bonds being broken/decomposition

Accept reverse argument e.g.

• compound A, as the other compounds have

less London forces as branching increases

• so surface area/points of contact

(of molecules) decreases

Question

Answer Additional Guidance Mark

Number

2(c) An explanation that makes reference to the following points: Allow differences in electronegativities for references to (3)

polar/non-polar bonds

CCl4, CHCl3 C6H14

• effect on the stream of liquid by CCl4, CHCl3 and C6H14 (1) Deflection X ✓ X

Bond ✓ ✓ *X

• (because of) bond polarity in CCl4, CHCl3 and C6H14 (1) polarity

Molecular X ✓ *(X)

• (resulting in) molecular non-polar /polarity due to polarity because because

shape (1) symmetrical non-symmetrical

Score either rows or columns, awarding the higher score

* For hexane only, allow reference to non-polar bonds to

imply non-polar molecule but not vice versa

Allow no dipole moment/vectors cancel for symmetry

Allow reference to dipoles cancel for symmetry

(Total for Question 2 = 8 marks)

How to answer it

Overall Question Difficulty: Medium

Intermolecular Forces and Molecular Polarity Study Guide

What this question tests

This question assesses your understanding of physical chemistry and bonding principles. Specifically, it targets the origin of London forces (instantaneous dipole–induced dipole forces), how molecular branching and surface area affect boiling temperatures in structural isomers, and how bond polarity combined with molecular symmetry determines overall molecular polarity and deflection in an electrostatic field.

Question (a)

Explain how London forces arise. (3 marks)

✅ Model Answer

  • Step 1: Random movement of electrons creates a temporary (instantaneous) uneven distribution of electron density within a molecule.
  • Step 2: This produces an instantaneous (or temporary) dipole in the first molecule.
  • Step 3: This temporary dipole induces a dipole in a neighbouring/adjacent molecule, leading to an electrostatic attraction.

🧠 Exam Technique & Mark Breakdown

To secure all 3 marks, you must follow the logical sequence of events:

  • Mark 1: Mentioning electron movement and uneven/asymmetrical distribution.
  • Mark 2: Stating the formation of an instantaneous/temporary dipole.
  • Mark 3: Explaining the induction of a dipole in a neighbouring molecule.

❌ Common Errors & Pitfalls

  • Permanent Dipoles: Never mention permanent dipoles when discussing non-polar alkanes. This loses marks instantly.
  • Atom vs Electron: Vague references to "atoms moving" instead of electron clouds shifting will fail to score Mark 1.

💡 Key Knowledge

London forces exist between all molecules (polar or non-polar). They are weaker than permanent dipole-dipole interactions and hydrogen bonds, but their cumulative effect increases significantly with larger molecular size and greater surface contact area.

Total for (a): 3 marks

Question (b)

Explain which of the compounds A–D will have the highest boiling temperature. (2 marks)

✅ Correct Answer

Compound A has the highest boiling temperature because it is unbranched, meaning it has a greater surface area (or more points of contact between molecules), resulting in stronger London forces that require more energy to overcome.

🧠 Exam Technique & Mark Breakdown

Full marks require linking structure directly to intermolecular force strength:

  • Mark 1: Identifying compound A and noting it has less/least branching or greater London forces.
  • Mark 2: Explaining that increased surface area or closer molecular packing allows for more points of contact.

❌ Common Errors & Pitfalls

  • Covalent Bonds: Never state that covalent bonds are broken during boiling. Examiners penalise this heavily.
  • Incorrect Reason: Do not claim compound A has "more electrons"—all isomers A–D share the exact same molecular formula ( C₆H₁₄ ) and therefore the same total number of electrons!

💡 Key Knowledge

As branching increases, molecules become more spherical, reducing the surface contact area between adjacent molecules. This decreases the magnitude of London forces and lowers the boiling temperature.

Total for (b): 2 marks

Question (c)

Explain whether or not each of these liquids will be deflected in this experiment. (3 marks)

✅ Correct Answer Summary

  • CCl₄ (Tetrachloromethane): Not deflected (non-polar molecule due to symmetrical shape, despite polar C-Cl bonds).
  • CHCl₃ (Trichloromethane): Deflected (polar molecule due to non-symmetrical shape and polar C-Cl/C-H bonds).
  • C₆H₁₄ (Hexane): Not deflected (non-polar molecule with non-polar bonds).

🧠 Exam Technique & Mark Breakdown

Marks are awarded across three analytical criteria:

  • Mark 1: Stating correct deflection outcomes for the three liquids.
  • Mark 2: Referencing bond polarity (difference in electronegativities creating polar bonds).
  • Mark 3: Explaining overall molecular polarity/symmetry (dipoles cancelling out vs. a net dipole moment).

❌ Common Errors & Pitfalls

  • Assuming Polar Bonds = Polar Molecule: Students often see polar C-Cl bonds in CCl₄ and incorrectly assume the liquid is polar. You must account for 3D molecular geometry and symmetry where bond dipoles cancel out.

💡 Key Knowledge

Charged rods attract polar molecules because the permanent dipole aligns with the electrostatic field, pulling the stream sideways. Non-polar liquids ( CCl₄ and C₆H₁₄ ) experience no net electrostatic attraction and flow straight down.

Total for (c): 3 marks

Topics

Physical Chemistry · Topic 2: Bonding and Structure

Question and mark scheme from the Edexcel A-Level Chemistry examination, Paper 3, June 2024. QuestionVault is an independent revision resource; questions remain the copyright of the awarding body.