Acetoacetic ester pathway

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Can someone explain question number 2 and why the answer is not 3-hexanone?

The reaction shown forms a ketone at the second carbon. "R" can be any hydrocarbon backbone. Regardless, the ketone will be right next to the terminal carbon, which is a 2-ketone. 2-hexanone is the only possible product.

3-hexanone requires the ketone to be at the third carbon from the end. That product just can't form via "reaction 2"
 

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