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<a accesskey="3" href="page.php?w=SN2_reaction&amp;p=2">3.Next</a>
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<p>The <b>bimolecular nucleophilic substitution</b> (<b>S<sub>N</sub>2</b>) is a type of <a href="page.php?w=reaction_mechanism">reaction mechanism</a> that is common in <a href="page.php?w=organic_chemistry">organic chemistry</a>. In the S<sub>N</sub>2 reaction, a strong <a href="page.php?w=nucleophile">nucleophile</a> forms a new bond to an <a href="page.php?w=orbital_hybridisation">sp<sup>3</sup></a>-hybridised carbon atom via a backside attack, all while the <a href="page.php?w=leaving_group">leaving group</a> detaches from the reaction center</p><p>
<a accesskey="3" href="page.php?w=SN2_reaction&amp;p=2">3.Next</a>
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