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Aldehydes and ketones (A-level only)
This A-level-only topic develops carbonyl chemistry through oxidation, reduction and nucleophilic addition.
4
Objectives
20
Flashcards
20
Questions
90 min
Study time
AQAA LevelChemistryOrganic chemistry
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Syllabus checklist
What you need to know
4 objective pages available
Aldehydes and ketones (A-level only)4 objectives
- Name and represent aldehydes and ketones.
- Use Tollens' and Fehling's reagents to distinguish aldehydes from ketones.
- Explain oxidation of aldehydes to carboxylic acids.
- Outline nucleophilic addition reactions of carbonyl compounds.
Key terms
aldehydeketonecarbonyl groupTollens' reagentFehling's reagentAldehydeCarboxylic AcidOxidation Reactionnucleophilic additioncarbonyl compoundnucleophile
Exam tips
- Naming Aldehydes and Ketones: Explain clearly by remember that aldehydes are named with the suffix '-al' and ketones with '-one'. Link the point to Aldehydes and ketones (A-level only), then state the evidence, calculation, mechanism, observation, or conclusion required by the question.
- Representing Carbonyl Compounds: Use structural formulas to represent aldehydes and ketones, ensuring to include the carbonyl group (C=O).
Common mistakes
- Incorrect Naming of Aldehydes: Remember that aldehydes are named with the suffix '-al' (e.g., ethanal), while ketones use '-one' (e.g., propanone).
- Misrepresentation of Structural Formulae: Ensure that the carbonyl group is correctly placed at the terminal position for aldehydes (e.g., CH3CHO for ethanal) and in the middle for ketones (e.g., CH3COCH3 for propanone).
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