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About Akeane

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  1. Thank you for your reply! I understand that you need to look at the stability of the resulting conjugate base to determine which is the most acidic proton. To do this, you need to consider the type of atom the proton is attached to (the more electronegative, the better), whether there are resonance structures that can delocalize the charge, whether there is the possibility of induction, and finally, the type of orbital. According to these criteria, I narrowed it down to the hydrogens attached to either C4 or C5 on the ring.I chose one attached to C5 because it is closest to the pi bond
  2. Which is the most acidic proton in 2-methyl-2-cyclopenten-1-one, and why?
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