Among the aromatic isomers with the molecular formula $C_8H_8O$,one isomer $X$ gives the iodoform test,while another isomer $Y$ gives the Benedict's test. What are the structures of $X$ and $Y$ respectively?

  • A
    $X = \text{Acetophenone}, Y = \text{Phenylacetaldehyde}$
  • B
    $X = \text{Acetophenone}, Y = \text{Benzaldehyde}$
  • C
    $X = o-\text{Methylbenzaldehyde}, Y = \text{Phenylacetaldehyde}$
  • D
    $X = p-\text{Methylbenzaldehyde}, Y = \text{Acetophenone}$

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The reagent used to distinguish between acetaldehyde and benzaldehyde is

Consider the following sequence of reactions:
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