CIE A Level Chemistry

Revision Notes

Syllabus Edition

First teaching 2020

Last exams 2024

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7.8.2 Multi-step Synthetic Routes

Test Yourself

Multi-Step Synthetic Routes

  • A large number of organic products are made from a few starting compounds using appropriate reagents and conditions
  • Knowing how organic functional groups are related to each other is key to the synthesis of a given molecule
  • The main functional groups you need to know are
    • Alkanes
    • Alkenes
    • Haloalkanes
    • Nitriles
    • Amines
    • Alcohols
    • Carbonyls (aldehydes & ketones)
    • Hydroxynitriles
    • Carboxylic acids
    • Esters
    • Acyl chlorides
    • Primary and secondary amides

Exam Tip

You also need to be able to identify the functional groups of these chemicals in structures that are given to you

Aliphatic Reaction Pathways

  • The key interconversions between functional groups are summarised here:

Aliphatic Reactions Table

6-8-2-aliphatic-reactions-table-1

Aromatic Reaction Pathways

  • The key aromatic reactions are summarised here:

Aromatic Reactions Table

6-8-2-aromatic-reactions-table

Designing a Reaction Pathway

  • The given molecule is usually called the target molecule and chemists try to design a synthesis as efficiently as possible
  • Designing a reaction pathway starts by drawing the structures of the target molecule and the starting molecule
  • Determine if they have the same number of carbon atoms
    • If you need to lengthen the carbon chain you will need to put on a nitrile group by nucleophilic substitution

  • Work out all the compounds that can be made from the starting molecule and all the molecules that can be made into the target molecule
    • Match the groups they have in common and work out the reagents and conditions needed

Worked example

Suggest how the following synthesis could be carried out:

Ethene to 1-aminopropane

Answer 

Organic synthesis WE Answer 2, downloadable AS & A Level Chemistry revision notes

Exam Tip

Sound knowledge of all of the different reactions is beneficial as the A-level course simply states that you should be able to design a multistage synthesis

Past papers generally go to four steps in a multistep reaction although there is no clear limit stated

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Francesca

Author: Francesca

Fran studied for a BSc in Chemistry with Forensic Science, and since graduating taught A level Chemistry in the UK for over 11 years. She studied for an MBA in Senior Leadership, and has held a number of roles during her time in Education, including Head of Chemistry, Head of Science and most recently as an Assistant Headteacher. In this role, she used her passion for education to drive improvement and success for staff and students across a number of subjects in addition to Science, supporting them to achieve their full potential. Fran has co-written Science textbooks, delivered CPD for teachers, and worked as an examiner for a number of UK exam boards.