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<p><a href="page.php?w=carbon">carbon</a>, forming a (<b>2</b>) <a href="page.php?w=Tetrahedral_carbonyl_addition_compound">tetrahedral intermediate</a>. The intermediate collapses, causing [1,2]-<a href="page.php?w=aryl">aryl</a> migration, <a href="page.php?w=hydroxide">hydroxide</a> <a href="page.php?w=elimination_reaction">elimination</a>, and formation of a (<b>3</b>) phenyl <a href="page.php?w=ester">ester</a>. The phenyl ester is subsequently <a href="page.php?w=hydrolysis">hydrolyzed</a>: nucleophilic addition of hydroxide ion from solution</p><p>
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