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<a accesskey="3" href="page.php?w=anomeric_effect&amp;p=2">3.Next</a>
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<p><a href="page.php?w=Image%3A%3F-_and_%3F-D-glucopyranose.svg">thumb</a>In <a href="page.php?w=organic_chemistry">organic chemistry</a>, the <b>anomeric effect</b> or <b>Edward-Lemieux effect</b> (after <a href="page.php?w=J._T._Edward">J. T. Edward</a> and <a href="page.php?w=Raymond_Lemieux">Raymond Lemieux</a>) is a <a href="page.php?w=stereoelectronic_effect">stereoelectronic effect</a> describing the tendency for vicinal <a href="page.php?w=heteroatom">heteroatomic</a> <a href="page.php?w=substituent">substituent</a>s of a cyclic heteroatom</p><p>
<a accesskey="3" href="page.php?w=anomeric_effect&amp;p=2">3.Next</a>
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