An ester $(A)$ with molecular formula $C_9H_{10}O_2$ was treated with excess of $CH_3MgBr$ and the complex so formed was treated with $H_2SO_4$ to give an olefin $(B)$. Ozonolysis of $(B)$ gave a ketone with molecular formula $C_8H_8O$ which shows positive iodoform test. The structure of $(A)$ is

  • A
    $C_6H_5COOC_2H_5$
  • B
    $C_2H_5COOC_6H_5$
  • C
    $CH_3COOCH_2C_6H_5$
  • D
    $C_6H_5CH_2COOCH_3$

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Similar Questions

Which product is formed when the compound $C_6H_5CHO$ is treated with concentrated $KOH$ solution?

Assertion $(A)$: Aldehydes are more reactive than ketones towards nucleophilic addition reactions.
Reason $(R)$: In aldehydes,carbonyl carbon is less electrophilic compared to ketones.
The correct answer is

Explain the different oxidation reactions of aldehydes and ketones.

Cannizzaro reaction is an example of:

$(CH_3)_3CCHO$ does not undergo aldol condensation due to

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