What happens when urea is heated with dilute naoh?
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Explanation:
Urea can be attacked by nucleophiles like any carbonyl. The immediate intermediate is a tetrahedral orthoacid which will break down to liberate ammonia once. The same process can be repeated a second time to liberate the second molecule of ammonia.
hydrolysis of urea
Technically, this is a hydrolysis catalysed by hydroxide. Hydroxide may be the reactive species but it is regenerated in the course of the reaction.
For urea to tautomerise to ammonium cyanate, a significant rearrangement and breaking a C−N bond would be required. Neither is likely in any way.
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