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Making a primary amine
The reaction happens in two stages. In the first stage, a salt is formed - in this case, ethylammonium bromide. This is just like ammonium bromide, except that one of the hydrogens in the ammonium ion is replaced by an ethyl group.
There is then the possibility of a reversible reaction between this salt and excess ammonia in the mixture.
The ammonia removes a hydrogen ion from the ethylammonium ion to leave a primary amine - ethylamine.
The more ammonia there is in the mixture, the more the forward reaction is favoured.
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