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<p>the rate of dehalogenation for alkyl halide also varies with <a href="page.php?w=steric">steric</a> environment and follows this trend:  primary > secondary > tertiary halides.</p>

<p><big>Applications</big></p>
<p>Since organochlorine compounds are the most abundant organohalides, most dehalogenations entail manipulation of C-Cl bonds.</p>

<p><big>Organic synthesis</big></p>
<p>Of some interest in <a href="page.php?w=organic_synthesis">organic synthesis</a>, electropositive metals react with many organic halides in a <a href="page.php?w=metal-halogen_exchange">metal-halogen exchange</a>:<br/></p><p>
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