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Two students are given 3-oxobutanoic acid below and asked to prepare 2-methyl-3-oxobutanoic acid. The first student...

Two students are given 3-oxobutanoic acid below and asked to prepare 2-methyl-3-oxobutanoic acid.

The first student recognizes this as the first step of the acetoacetic ester synthesis. He treats the starting material with sodium methoxide followed by methyl iodide. He isolates compound A, but 1H NMR analysis shows this is not the desired material. Elemental analysis shows it has the same molecular formula as the 2-methyl-3-oxobutanoic acid. What is compound A?

The second student recognizes an extra step is needed first. She treats the starting material with diazomethane and isolates compound B. She then treats compound B with sodium methoxide followed by methyl iodide and isolates compound C. Draw compounds B and C.

Compound C can be converted to the 2-methyl-3-oxobutanoic acid using what reagent?

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