Problem: Starting from ethyl acetoacetate, show how the following target compound can be prepared using the acetoacetic ester synthesis. Note: A reaction mechanism (i.e.; arrow-pushing) is not required.  

🤓 Based on our data, we think this question is relevant for Professor Golder's class at UW-SEATTLE.

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Starting from ethyl acetoacetate, show how the following target compound can be prepared using the acetoacetic ester synthesis. Note: A reaction mechanism (i.e.; arrow-pushing) is not required.

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Our tutors have indicated that to solve this problem you will need to apply the Beta-Dicarbonyl Retrosynthesis concept. If you need more Beta-Dicarbonyl Retrosynthesis practice, you can also practice Beta-Dicarbonyl Retrosynthesis practice problems.

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Based on our data, we think this problem is relevant for Professor Golder's class at UW-SEATTLE.