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<p>alkenes are subject to strain resulting from distortion of the sp<sup>2</sup>-hybridized carbon centers.  Illustrative is <a href="page.php?w=Buckminsterfullerene">C<sub>60</sub></a> where the carbon centres are pyramidalized.  This distortion enhances the reactivity of this molecule.  Angle strain also is the basis of <a href="page.php?w=Bredt%27s_rule">Bredt's rule</a> which dictates that bridgehead carbon centers are not incorporated in alkenes because the resulting alkene would be subject to extreme angle strain.</p>

<p>Small trans-cycloalkenes</p><p>
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