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<p>on carbon 5 (C-5) of a sugar with the <a href="page.php?w=aldehyde">aldehyde</a> at carbon 1. This forms an intramolecular <a href="page.php?w=hemiacetal">hemiacetal</a>. If reaction is between the C-4 hydroxyl and the aldehyde, a <a href="page.php?w=furanose">furanose</a> is formed instead. The pyranose form is thermodynamically more stable than the furanose form, which can be seen by the distribution of these two cyclic forms in solution.</p>

<p><big>History</big></p>
<p> <a href="page.php?w=Hermann_Emil_Fischer">Hermann Emil Fischer</a> won the <a href="page.php?w=Nobel_Prize_in_Chemistry">Nobel Prize in Chemistry</a></p><p>
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