how do you kow which acitic proton to take off?

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It's always going to be the alpha hydrogen when you have an ester or ketone
 
Anyone know which alpha is taken off? Should there be two solutions to the problem?
 
Anyone know which alpha is taken off? Should there be two solutions to the problem?

I think there would be two solutions. The other product formed should be the same as the one in the answer, but with the ethyl group moved over one carbon to the left.
 
Easy there are two acidic hydrogens but the molecule is symetrical and therefore which ever one you take off either one will gave same reslt. Take a pen and paper and try it, you'll see.
 
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