OCR A-Level Chemistry AS Breadth in chemistry (01), November 2021: Question 15

1 mark · Medium difficulty · Multiple Choice

Identify which structural isomer of C7H16 has the weakest induced dipole-dipole interactions (London forces) among four given options.

Practise this question

Question

Multiple-choice question 15 asks which structural isomer of C7H16 has the weakest induced dipole-dipole interactions (London forces). Four options are provided: A, 2,3-dimethylpentane; B, 3-ethylpentane; C, 2-methylhexane; D, 2,2,3-trimethylbutane. An answer box is shown at the bottom with a 1-mark allocation.
Question text

15 Which structural isomer of C7H16 has the weakest induced dipole–dipole interactions (London

forces)?

A 2,3-dimethylpentane

B 3-ethylpentane

C 2-methylhexane

D 2,2,3-trimethylbutane

Your answer [1]

Mark scheme

Show the mark scheme The mark scheme shows question number 15 with the correct answer as letter D, worth 1 mark.

15 D 1 AO2.1

How to answer it

Structural Isomers and London Forces in Alkanes

📌 What this question tests

This question assesses your understanding of intermolecular forces—specifically induced dipole-dipole interactions (London forces)—and how molecular branching and chain length affect the strength of these forces in structural isomers of alkanes (formula C₇H₁₆ ).

Question 15 (Multiple Choice)

Identifying the Isomer with the Weakest London Forces

✅ Correct Answer

D: 2,2,3-trimethylbutane

All given options are structural isomers with the same molecular formula ( C₇H₁₆ ), meaning they have the same number of electrons. However, 2,2,3-trimethylbutane is the most branched structure, giving it a nearly spherical shape with the smallest surface area of contact.

💡 Key Knowledge

  • London forces arise from temporary, fluctuating dipoles caused by the random movement of electrons.
  • Greater surface area = more points of contact between molecules = stronger London forces.
  • Increased branching creates a more spherical/compact molecular shape, reducing the surface area of contact and decreasing the strength of London forces.

🧠 Exam Technique

When comparing isomers with the same molecular formula, ignore the molar mass (it is identical for all choices!). Instead, look directly at the IUPAC names to determine the amount of branching. The isomer with the most methyl/alkyl branches packed onto the shortest main carbon chain will have the weakest intermolecular forces.

❌ Common Errors

Students often incorrectly assume that longer names or more substituents mean stronger forces overall. Some mistakenly confuse London forces with permanent dipole-dipole interactions or hydrogen bonding, forgetting that non-polar alkanes only experience induced dipole-dipole interactions.

Mark Allocation: [1 mark] awarded for selecting option D.

Topics

Module 4: Core organic chemistry · 4.1 Basic concepts and hydrocarbons

Question and mark scheme from the OCR A-Level Chemistry examination, AS Breadth in chemistry (01), November 2021. QuestionVault is an independent revision resource; questions remain the copyright of the awarding body.