- Students should be able to critically analyse given synthetic routes and determine whether appropriate reagents and reaction conditions are used
- Students should also be able to predict possible by-product of a synthetic reaction
The correct answer is D
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.
The correct answer is C
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.