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<p>Cyclic hemiacetals often form readily, especially when they are 5- and 6-membered rings. In this case, a hydroxy group reacts with a carbonyl group within the same molecule to undergo an <a href="page.php?w=Intramolecular_reaction">intramolecular cyclization reaction</a>.</p>

<p><big>Hemiacetals in nature</big></p>
<p>Hemiacetals commonly exist in nature as <a href="page.php?w=aldose">aldose</a>s such as <a href="page.php?w=glucose">glucose</a>, and hemiketals commonly exist in nature as <a href="page.php?w=ketose">ketose</a>s such as <a href="page.php?w=fructose">fructose</a>.</p><p>
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