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Hi, ok so i just revising chem paper 3, and thought, hey, i should write what i just learnt on here! So here is the explanation of the alkaline hydrolysis of esters! Is this on the syllabus? I don't know lol but its in my chemistry book so worth learning
Esters can be hydrolysed to an alcohol and the sodium salt of the carboxylic acid (NOT the carboxylic acid)
How? Well, we use dilute sodium hydroxide (aq) and heat the mixture UNDER REFLUX.
So,
ester + sodium hydroxide --> alcohol + sodium carboxylate
Let me give you an example,
ethyl ethanoate + sodium hydroxide --> ethanol + sodium ethanoate
don't forget, we must heat it under reflux, as we do with all hydrolysises
Ok. Now, how do we get the carboxylic acid instead of sodium carboxylate? Easy! All you have to do is add HCl (aq) to the hydrolysis products and voila! The Carboxylic acid.
I hope I helped!
Esters can be hydrolysed to an alcohol and the sodium salt of the carboxylic acid (NOT the carboxylic acid)
How? Well, we use dilute sodium hydroxide (aq) and heat the mixture UNDER REFLUX.
So,
ester + sodium hydroxide --> alcohol + sodium carboxylate
Let me give you an example,
ethyl ethanoate + sodium hydroxide --> ethanol + sodium ethanoate
don't forget, we must heat it under reflux, as we do with all hydrolysises
Ok. Now, how do we get the carboxylic acid instead of sodium carboxylate? Easy! All you have to do is add HCl (aq) to the hydrolysis products and voila! The Carboxylic acid.
I hope I helped!