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<p>to another oxygen (can be N or S or a <a href="page.php?w=halogen">halogen</a>), called an <a href="page.php?w=Acyl_group">acyl</a> group. The nucleophile attacks the carbon causing the double bond to break into a single bond. The double can then reform, kicking off the leaving group in the process.</p>

<p>Aromatic substitution occurs on compounds with systems of double bonds connected in rings. See <a href="page.php?w=Aromatic_compound">aromatic compounds</a> for more.</p>

<p><big> Electrophilic substitution </big></p>
<p><a href="page.php?w=Electrophile">Electrophile</a>s</p><p>
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