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
    $C_6H_5COOC_6H_5$
  • C
    $C_6H_5COOCH_3$
  • D
    $p-CH_3O-C_6H_4-COCH_3$

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Similar Questions

The major product of the following reaction is

Match List-$I$ with List-$II$.
List-$I$ Reaction List-$II$ Reagents
$A$. Hoffmann Degradation $I$. Conc. $KOH, \Delta$
$B$. Clemmensen reduction $II$. $CHCl_3, NaOH / H_3O^{+}$
$C$. Cannizzaro reaction $III$. $Br_2, NaOH$
$D$. Reimer-Tiemann reaction $IV$. $Zn-Hg / HCl$

The correct option for the above reaction is

Draw structures of the following derivatives:
$(i)$ The $2,4-$dinitrophenylhydrazone of benzaldehyde
$(ii)$ Cyclopropanone oxime
$(iii)$ Acetaldehyde dimethyl acetal
$(iv)$ The semicarbazone of cyclobutanone
$(v)$ The ethylene ketal of hexan$-3-$one
$(vi)$ The methyl hemiacetal of formaldehyde

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What are $X$ and $Y$ respectively in the following reactions?
$C_6H_5COOH \xrightarrow{X} C_6H_5CHO$
$C_6H_5CHO \xrightarrow[OH^-, 293 \ K]{C_6H_5COOH} Y \text{ (Major product)}$

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