Revision Notes MCQ Bank SAQ Bank Study Cards Courses Teachers Blog
Cambridge International AS & A Level Chemistry – Organic Chemistry and Analysis

Topic 37
Analytical
Techniques

Topic 37 covers thin-layer chromatography and Rf values, gas–liquid chromatography, retention times and percentage composition, carbon-13 NMR, and proton NMR with chemical shifts, relative peak areas, splitting patterns, TMS, deuterated solvents and proton exchange with D₂O.

Exam Paper
Paper 4
9701 A Level
Learning Outcomes
37.1.1 – 37.4.5
4 sections covered
Sub-topics
4 lessons
Revision notes available
Exam Board
Cambridge
9701 (2025 onwards)

Revision Notes

4 revision notes, in the order the specification teaches them.

Summary Map

Download, print and revise the key facts of this topic at a glance.

Summary map

Download, print and revise the key facts of this topic at a glance.

Illustration of a summary map: compounds joined by reaction arrows
Summary map · PDF

Analytical Techniques Map

Cambridge International AS & A Level Chemistry · Topic 37 Analytical techniques

The whole section on one A4 page: thin-layer and gas chromatography, ¹³C and ¹H NMR, splitting and D₂O exchange.

Download the map6 key ideas + a data table · A4 portrait · print ready

© 2026 Online Learning System. For personal study: printing is allowed; editing, copying and redistribution are not.

Virtual Lessons

Recorded video lessons that teach the topic step by step.

Coming soon

The Virtual Lessons for Topic 37 Analytical Techniques are being recorded.

MCQ Bank

Multiple-choice papers on this topic, marked the moment you submit.

Coming soon

The MCQ papers for Topic 37 Analytical Techniques are being written.

SAQ Bank

Written, drawn and worked exam practice on this topic.

Coming soon

The exam practice papers for Topic 37 Analytical Techniques are being written.

Revision Game

Match reagents to products, with your board's reagents and conditions.

Coming soon

The revision game for Topic 37 Analytical Techniques is being built.

Study Cards

Pick a deck, then turn each card to check what you remember.

Specification

Every specification point in this topic, in the exam board's own words. Rate how confident you are with each one.

Cambridge no longer issues a data booklet: the data you need are given in each question, and the syllabus has a Data section.

Self-assessment · 26 points

Sign in to rate how confident you feel about each point. Your ratings are saved to your account, follow you to any device, and appear beside your KASP analytics, kept apart from your marks.

0 Confident0 Getting there0 Not yet26 Not rated

37.1.1

  1. a

    describe and understand the term stationary phase in thin-layer chromatography, for example aluminium oxide (on a solid support)

    Revise
  2. b

    describe and understand the term mobile phase in thin-layer chromatography; a polar or non-polar solvent

    Revise
  3. c

    describe and understand the term Rf value

    Revise
  4. d

    describe and understand the terms solvent front and baseline

    Revise

37.1.2

  1. 37.1.2

    interpret Rf values

    Revise

37.1.3

  1. a

    explain the differences in Rf values in terms of interaction with the stationary phase

    Revise
  2. b

    explain the differences in Rf values in terms of relative solubility in the mobile phase

    Revise

37.2.1

  1. a

    describe and understand the term stationary phase in gas/liquid chromatography; a high boiling point non-polar liquid (on a solid support)

    Revise
  2. b

    describe and understand the term mobile phase in gas/liquid chromatography; an unreactive gas

    Revise
  3. c

    describe and understand the term retention time

    Revise

37.2.2

  1. 37.2.2

    interpret gas/liquid chromatograms in terms of the percentage composition of a mixture

    Revise

37.2.3

  1. 37.2.3

    explain retention times in terms of interaction with the stationary phase

    Revise

37.3.1

  1. a

    analyse and interpret a carbon-13 NMR spectrum of a simple molecule to deduce the different environments of the carbon atoms present

    Revise
  2. b

    analyse and interpret a carbon-13 NMR spectrum of a simple molecule to deduce the possible structures for the molecule

    Revise

37.3.2

  1. a

    predict the number of peaks in a carbon-13 NMR spectrum for a given molecule

    Revise
  2. b

    explain the number of peaks in a carbon-13 NMR spectrum for a given molecule

    Revise

37.4.1

  1. a

    analyse and interpret a proton (1H) NMR spectrum of a simple molecule to deduce the different environments of proton present using chemical shift values

    Revise
  2. b

    analyse and interpret a proton (1H) NMR spectrum of a simple molecule to deduce the relative numbers of each type of proton present from relative peak areas

    Revise
  3. c

    analyse and interpret a proton (1H) NMR spectrum of a simple molecule to deduce the number of equivalent protons on the carbon atom adjacent to the one to which the given proton is attached from the splitting pattern, using the n + 1 rule (limited to singlet, doublet, triplet, quartet and multiplet)

    Revise
  4. d

    analyse and interpret a proton (1H) NMR spectrum of a simple molecule to deduce the possible structures for the molecule

    Revise

37.4.2

  1. a

    predict the chemical shifts of the protons in a given molecule

    Revise
  2. b

    predict the splitting patterns of the protons in a given molecule

    Revise

37.4.3

  1. 37.4.3

    describe the use of tetramethylsilane, TMS, as the standard for chemical shift measurements

    Revise

37.4.4

  1. 37.4.4

    state the need for deuterated solvents, e.g. CDCl3, when obtaining a proton NMR spectrum

    Revise

37.4.5

  1. a

    describe the identification of O–H protons by proton exchange using D2O

    Revise
  2. b

    describe the identification of N–H protons by proton exchange using D2O

    Revise