Aldehydes and Ketones

From the study guide

Course Outline

  1. Structures and Nomenclature
  2. Preparation Methods
  3. Properties and Nucleophilic Addition
  4. Grignard and Derivative Formation
  5. Redox Reactions and Tests
  6. Condensation and Aromatic Reactions
  7. Named Reactions and Conversions

1. Structures and Nomenclature

Key Concepts & Definitions

  • Aldehyde: has the general structure R–CHO, with the carbonyl carbon attached to at least one hydrogen atom
  • Ketone: has the general structure R–CO–R′, with the carbonyl carbon attached to two carbon groups
  • Carbonyl group: is C=O, and its polarity makes the carbonyl carbon electrophilic because oxygen is more electronegative

Essential Points

📌 The reactivity order is HCHO > RCHO > RCOR′ because aldehydes have less steric hindrance and fewer electron-donating alkyl groups than ketones.

Memory Hook

Aldehyde: carbonyl carbon bears H; ketone: carbonyl carbon bears two carbon groups.

2. Preparation Methods

Essential Points

  • Primary alcohols are oxidised to aldehydes, and aldehydes can be further oxidised to carboxylic acids.
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Practice quiz preview

1. Which structural feature identifies an aldehyde?

2. Which formula represents a ketone?

3. Why is the carbonyl carbon electrophilic?

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Flashcard preview

What is the general structure of an aldehyde?

R–CHO with carbonyl carbon attached to at least one hydrogen.

What is the general structure of a ketone?

R–CO–R′ with carbonyl carbon attached to two carbon groups.

What is the chemical formula of the carbonyl group?

C=O.

Why is the carbonyl carbon electrophilic?

Because oxygen is more electronegative, making the carbonyl polar.

Why are aldehydes more reactive than ketones?

They have less steric hindrance and fewer electron-donating alkyl groups.

What is the product of oxidising primary alcohols?

Aldehydes

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The practice quiz has 20 multiple-choice questions, each with an explanation. Use it to check what you know and find your gaps.

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