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(Solved): 2. Which compound when treated with \( \mathrm{NaOCH}_{3} \) followed by neutralization with aqueo ...



2. Which compound when treated with \( \mathrm{NaOCH}_{3} \) followed by neutralization with aqueous acid will produce this \

2. Which compound when treated with \( \mathrm{NaOCH}_{3} \) followed by neutralization with aqueous acid will produce this \( \beta \)-diketone? (A) (B) (C) (D) 3. If this steroid tetracarboxylic acid is heated, which carboxyl group will be readily lost as carbon dioxide? (A) \( \mathrm{CO}_{2} \mathrm{H} \) at \( \mathrm{C}-15 \) (B) \( \mathrm{CO}_{2} \mathrm{H} \) at \( \mathrm{C}-13 \) (C) \( \mathrm{CO}_{2} \mathrm{H} \) at \( \mathrm{C}-5 \) (D) \( \mathrm{CO}_{2} \mathrm{H} \) at \( \mathrm{C}-2 \)


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Solution: 2. -diketone is obtained by treating the compound (C) with NaOCH3 followed by neutralization with aque
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