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1. What is a structure based explanation for why acetamide is more stable than acetone. I'm pretty sure it has to do with resonance.

2. F. Draw the conjugate base for each compound below and draw the appropriate structures to explain the difference in N-H acidity pKa~9.5 pKa 16 N-H N-Halso for question F im fairly sure it has to do with resonance again but I not sure exactly why. could someone answer and explain?

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