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<p>outwards so that the inter-orbital angle is 104°.</p>

<p>The unusual structural properties of cyclopropane have spawned many theoretical discussions.  One theory invokes ?-<a href="page.php?w=aromaticity">aromaticity</a>: the stabilization afforded by delocalization of the six electrons of cyclopropane's three C-C ? bonds to explain why the strain of cyclopropane is "only" 27.6&nbsp;kcal/mol as compared to <a href="page.php?w=cyclobutane">cyclobutane</a> (26.2&nbsp;kcal/mol) with <a href="page.php?w=cyclohexane">cyclohexane</a> as reference</p><p>
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