Originally posted by babinski bob
Here's the CORRECT answer for the fxnl group acidity question
B-ketoester > acid chloride > aldehyde > ketone > ester > amide > amine
The stronger the e- withdrawing character of the carbonyl, the more acidic the alpha-hydrogen. Acid chlorides are more acidic than aldehydes, ketones, esters, amides, amines because of the electron withdrawing character. A general trend for the acidity of alpha H's is that they parallel C=O reactivity. So acid chlorides are more reactive than aldehydes which are more reactive than ketones which are more reactive than esters which are more reactive than amides.