Synthetic Routes (OCR AS Chemistry A)
Revision Note
Two-Stage Organic Synthetic Routes
It is possible to make a large number of organic products from a few starting compounds and the necessary 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
Alcohols
Carbonyls (aldehydes & ketones)
Carboxylic acids
Aliphatic Reaction Pathways
The key functional groups and their interconversions are summarised here:
The main reaction pathways at AS level
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:
Chloroethane to ethanoic acid
Answer
Examiner Tips and Tricks
At AS level, you will only be required to design a synthesis with two steps, i.e. reactant → intermediate → product
However, sound knowledge of all of the different reactions will be beneficial in the long run - especially as the A-level course simply states that you should be able to design a multistage synthesis
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