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A Level · Cambridge (CIE) · 9701

Name alcohols, aldehydes, ketones and carboxylic acids

Apply the characteristic suffixes and position rules for common oxygen-containing organic classes.

Section 13 · An introduction to AS Level organic chemistry

An introduction to AS Level organic chemistry · Cambridge 9701 · 13.1

AS Level; Cambridge International Chemistry 9701, 2025–2027 syllabus. Use the published functional-group scope and nomenclature limits; draw formula and mechanism evidence with correct connectivity, electron movement and stereochemistry. Written practice is self-checked

Before you begin

  • Use covalent structures, valency, molecular formulas, lone pairs, and single, double and triple bonds.

Work on paper. Try each question before revealing help, and explain why your method works.

Quick readiness check

Which suffix identifies an aldehyde?

What you will learn

  • Name alcohols with an -OH locant
  • Distinguish aldehyde and ketone suffixes
  • Name a carboxylic acid with its terminal group

Use the suffix that identifies the principal group

Alcohols use -ol and a locant if the hydroxyl group can occupy different positions, for example propan-1-ol and propan-2-ol.

Aldehydes use -al for terminal –CHO, as in propanal. Ketones use -one with a carbonyl locant where needed, as in butan-2-one. The aldehyde carbon is part of the parent chain and is at its end.

Carboxylic acids have a terminal -oic acid group

Carboxylic acids use -oic acid, for example ethanoic acid and propanoic acid. The carboxyl carbon is included in the parent chain and is assigned carbon 1, so its position is not usually written.

When identifying the class, distinguish an alcohol –OH from the –OH that is part of a –COOH carboxyl group.

Pause and explain

How should the carbon of a carboxyl group be counted?

Put the idea to work

Worked example

Name CH₃CH(OH)CH₃, CH₃CH₂CHO and CH₃COCH₂CH₃.

Show the worked solution
  1. The alcohol has three carbons and –OH at carbon 2.
  2. The aldehyde has three carbons and terminal –CHO.
  3. The ketone has four carbons with C=O at carbon 2 from the nearer end.

Answer The names are propan-2-ol, propanal and butan-2-one.

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From guided practice to a new situation

Write your answer and reasoning first. Use a hint only if you are stuck. The model solution is for self-checking; your written work is not automatically marked.

1 · Guided

Name CH₃CH₂CH₂OH.

Give me a hint

Count the parent and give the position of –OH.

Compare my reasoning
  1. There are three carbons.
  2. The –OH is on an end carbon, carbon 1.
  3. Use the alcohol suffix -ol.

Propan-1-ol.

Look for these in your work

  • Parent count
  • Hydroxyl locant
  • Suffix
2 · Independent

Name CH₃CH₂COCH₃.

Give me a hint

The carbonyl is inside the chain, so identify the ketone.

Compare my reasoning
  1. The parent has four carbons.
  2. Number from the end nearest C=O.
  3. The carbonyl is at carbon 2: butan-2-one.

Butan-2-one.

Look for these in your work

  • Ketone class
  • Four-carbon parent
  • Lowest carbonyl locant
3 · Transfer

A learner names CH₃CH₂COOH as propan-1-ol. Correct the name.

Give me a hint

Identify the complete functional group, including the carbonyl carbon.

Compare my reasoning
  1. The structure ends in –COOH, not an alcohol –OH group.
  2. Count the carboxyl carbon: there are three carbons total.
  3. Use the carboxylic acid suffix.

Propanoic acid.

Look for these in your work

  • Carboxyl group identified
  • Carbon count correct
  • Acid suffix used

Common mistakes

  • Calling an aldehyde a ketone because both have C=O
  • Giving a needless position for the carboxyl carbon
  • Omitting the alcohol locant when positional isomers exist
Recall without your notes

What can you explain now?

Which suffix identifies an aldehyde?

Compare with the explanation

-al

A terminal –CHO group is named with -al.

After trying it yourself, choose your next review. This is your self-assessment.

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Make it stick

How do you distinguish –OH in an alcohol from –OH within a carboxylic acid?

If you needed the solution, close it and solve the problem again from a blank page. A correct answer is stronger when you can explain the reason for each step.

Keep learning Chemistry

Course scope and assessment

Four hundred and forty-two original lessons map the published learning outcomes across AS Chemistry Topics 1–22 and A Level Topics 23–37, with guided, independent and transfer practice and explained answers. Every numbered subject-content topic and listed outcome tag now has a mapped lesson sequence. Topic 32 maps all 12 hydroxy-compound outcome tags in 11 lessons; Topic 33 maps all 15 carboxylic-acid and derivative outcome tags in 16 lessons; Topic 34 maps all 22 nitrogen-compound outcome tags in 20 lessons; Topic 35 maps all 12 polymerisation outcome tags in 16 lessons; Topic 36 maps all four organic-synthesis outcome tags in 14 lessons; Topic 37 maps all 22 chromatography and NMR outcome tags in 18 lessons. Cambridge's 2028–2030 Version 1 syllabus states that there are no significant changes which affect teaching from the preceding edition; the routes are aligned to that edition. This is 37 of the 37 numbered subject-content topics. Full cumulative exam assessment, Paper 3 laboratory competence, Paper 5 investigation practice and human subject-teacher review remain outstanding. Written practice is self-checked and does not certify exam readiness.

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