Dat destroyer ochem

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Aldehyde H's aren't acidic.

The electronegative O atom stabilizes the negative charge well for -OH groups.
 
For these type of problems, I first obviously look for like carboxy acids to be most acidic proton and if that doesn't work, I look for which proton is connected to a more electronegative atom. The more electronegative, the more acidic I think. Can anyone confirm?
 
I think how the compound would be after proton (H+) is removed. So I compare the conjugate base of each. Which one would be more basic after proton is removed? Whichever is the stronger base, has the weaker conjugate acid.
Hope that makes sense.
 
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