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<p>as the oxidant in the presence of a tungsten catalyst. </p>

<p><a href="page.php?w=1%2C7-Octadiene">1,7-Octadiene</a> is produced by <a href="page.php?w=ethenolysis">ethenolysis</a> of cyclohexene. Bromination gives 1,2-dibromocyclohexane.</p>

<p><big> Structure </big></p>
<p>Cyclohexene is most stable in a half-chair <a href="page.php?w=conformational_isomerism">conformation</a>, unlike the preference for a chair form of <a href="page.php?w=cyclohexane">cyclohexane</a>. One basis for the <a href="page.php?w=cyclohexane_conformation">cyclohexane conformation</a>al</p><p>
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