OCR A Level Chemistry

Revision Notes

6.8.2 Synthetic Routes

Test Yourself

Multi-Stage Organic 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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