An ester $(A)$ with molecular formula $C_9H_{10}O_2$ is reacted with an excess of $CH_3MgBr$. The resulting product is treated with concentrated $H_2SO_4$ to form an olefin $(B)$. Ozonolysis of $(B)$ yields a ketone with the formula $C_8H_8O$. What is the structure of $(A)$?

  • A
    $C_6H_5COOC_2H_5$
  • B
    $CH_3OCH_2COC_6H_5$
  • C
    $CH_3COC_6H_4COCH_3$
  • D
    $C_6H_5COOC_6H_5$

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