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<p>acid bears a carbocation-stabilizing side-substituent at the ? position, but only sometimes otherwise.<br/>
:</p>

<p><big>Applications</big></p>
<p>Kolbe electrolysis has a few industrial applications.  The reaction typically yields <50%.</p>

<p>In one example, <a href="page.php?w=sebacic_acid">sebacic acid</a> has been produced commercially by Kolbe electrolysis of <a href="page.php?w=adipic_acid">adipic acid</a>.</p>

<p>Kolbe electrolysis has been examined for converting biomass into <a href="page.php?w=biodiesel">biodiesel</a> and for <a href="page.php?w=Grafting%28chemistry%29">grafting</a> of carbon electrodes.</p>

<p><big>See also</big></p>
<p>
* <a href="page.php?w=Electrosynthesis">Electrosynthesis</a><br/>
* <a href="page.php?w=Wurtz_reaction">Wurtz reaction</a><br/>
* <a href="page.php?w=Hunsdiecker_reaction">Hunsdiecker reaction</a></p>

<p><big> References </big></p>
<p><big>Further reading</big></p>
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*<br/>
*</p>

<p><big> External links</big></p>
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* </p>

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