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<a accesskey="3" href="page.php?w=Hofmann_rearrangement&amp;p=2">3.Next</a>
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<p>The <b>Hofmann rearrangement</b> (<b>Hofmann degradation</b>) is the <a href="page.php?w=organic_chemistry">organic</a> reaction of a primary <a href="page.php?w=amide">amide</a> to a primary <a href="page.php?w=amine">amine</a> with one less <a href="page.php?w=carbon">carbon</a> atom. The reaction involves <a href="page.php?w=organic__oxidation">oxidation</a> of the nitrogen followed by <a href="page.php?w=rearrangement_reaction">rearrangement</a> of the carbonyl and nitrogen to give an <a href="page.php?w=isocyanate">isocyanate</a> intermediate.</p><p>
<a accesskey="3" href="page.php?w=Hofmann_rearrangement&amp;p=2">3.Next</a>
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