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<a accesskey="3" href="page.php?w=solvolysis&amp;p=2">3.Next</a>
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<p>In <a href="page.php?w=chemistry">chemistry</a>, <b>solvolysis</b> is a type of <a href="page.php?w=nucleophilic_substitution">nucleophilic substitution</a> (S1/S2) or  <a href="page.php?w=elimination_reaction">elimination</a> where the <a href="page.php?w=nucleophile">nucleophile</a> is a <a href="page.php?w=solvent">solvent</a> molecule. Characteristic of S1 reactions, solvolysis of a <a href="page.php?w=chirality_%28chemistry%29">chiral</a> reactant affords the <a href="page.php?w=racemate">racemate</a>. Sometimes however, the stereochemical</p><p>
<a accesskey="3" href="page.php?w=solvolysis&amp;p=2">3.Next</a>
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