Synthetic Routes (Cambridge (CIE) A Level Chemistry): Revision Note
Analysis of Synthetic Routes
Worked Example
The synthesis of compound X takes place in 2 steps:
OHCCH2CHO | intermediate | HO2CCH(OH)CH2CH(OH)CO2H | ||
|
|
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| compound X |
Which reagents could be used for this synthesis?
Answer:
The first step involves a nucleophilic addition of CN- using NaCN as catalyst and heat to form a hydroxynitrile
In the second step, the nitrile is refluxed with dilute aqueous sulfuric acid causing hydrolysis of the nitrile forming a carboxylic acid and ammonium salt
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Worked Example
The synthesis of hexanoic acid takes place in 2 steps
1-chloropentane | compound Z | hexanoic acid |
Which reagents could be used for this synthesis?
Answer:
Halogenoalkanes can undergo nucleophilic substitution with ethanolic KCN in which the CN- ion acts as a nucleophile and replaces the chlorine atom in 1-chloropentane to form a nitrile.
The treatment of nitriles with concentrated hydrochloric acid will produce a carboxylic acid and an ammonium salt.
In this case, hexanoic acid and ammonium chloride will be formed.
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