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<p>base, an <a href="page.php?w=alpha_hydrogen">?-hydrogen</a> in an aldehyde is weakly <a href="page.php?w=acid">acid</a>ic with a <a href="page.php?w=pKa">p''K''<sub>a</sub></a> near 17.  This acidification of the ?-hydrogen in aldehyde is attributed to:<br/>
* the electron-withdrawing quality of the formyl center and<br/>
* the fact that the conjugate base, an <a href="page.php?w=enolate">enolate</a> anion, delocalizes its negative charge.The formyl proton itself does not readily undergo deprotonation.</p>

<p><big>Enolization</big></p>
<p>Aldehydes (except</p><p>
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