AeroLab Reading room

CHEM / AS level

Organic reactions and mechanisms

Functional groups organise reactions of hydrocarbons, halogenoalkanes, alcohols, carbonyl compounds, acids, esters and nitriles. Structural and stereoisomerism describe different relationships.

Learning objectives

The big idea

Functional groups organise reactions of hydrocarbons, halogenoalkanes, alcohols, carbonyl compounds, acids, esters and nitriles. Structural and stereoisomerism describe different relationships.

Mechanisms track electrons using curly arrows. Distinguish nucleophiles, electrophiles and radicals; conditions and reagents determine whether addition, substitution, elimination or oxidation dominates.

Worked example

Which product forms when ethanol is fully oxidised under suitable reflux conditions?

Follow the solution

A primary alcohol can be oxidised through an aldehyde to a carboxylic acid under appropriate conditions.

Investigate and explain

Predict the worked result before calculating. Change one input, record the new result, and explain which assumptions still hold.

Related interactive model. Compare its assumptions with the explanation; it is not a complete syllabus lesson.

Open the interactive investigation

Check your understanding

1. What does a curly arrow represent?

  1. Movement of an electron pair
  2. Movement of a nucleus
  3. Heat flow
Check the answer and reasoning

Movement of an electron pair

The arrow starts at an electron pair or bond and ends where the pair moves.

2. Which product forms when ethanol is fully oxidised under suitable reflux conditions?

  1. Ethene always
  2. Ethanoic acid
  3. Ethane
Check the answer and reasoning

Ethanoic acid

A primary alcohol can be oxidised through an aldehyde to a carboxylic acid under appropriate conditions.

3. Are constitutional isomers identical compounds?

  1. Yes
  2. Only with the same formula
  3. No
Check the answer and reasoning

No

They share a molecular formula but have different atom connectivity and may have different properties.