Which of the following compounds does not react with concentrated alkali to give the corresponding alcohol and salt of carboxylic acid?

  • A
    Benzaldehyde
  • B
    Trimethylacetaldehyde
  • C
    Dimethyl acetaldehyde
  • D
    Formaldehyde

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Ethylene is converted to $X$ on passing through a mixture of an acidified aqueous solution of palladium chloride and cupric chloride. Which of the following reagents readily take part in addition reaction with $X$?

$(A)$ $\xrightarrow{NH_2OH} (B)$ $\xrightarrow{H_2SO_4} (C)$ $\xrightarrow{H_3O^{\oplus}} (D) + (E)$ $\xrightarrow{CHCl_3, KOH} CH_3-NC$ (carbylamine test). $(D)$ $\xrightarrow{SOCl_2} (F)$ $\xrightarrow{(i) PhMgBr \text{ (excess) } (ii) H^{\oplus}} (G)$ $\xrightarrow[\Delta]{H^{\oplus}} (H)$ $\xrightarrow{CH_2I_2, Zn/Cu} \text{1,1-diphenylcyclopropane}$. The molecular weight of compound $(A)$ is:

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Assertion : Benzaldehyde is more reactive than ethanol towards nucleophilic attack.
Reason : The overall effect of $-I$ and $+R$ effect of phenyl group decreases the electron density on the carbon atom of $>C=O$ group in benzaldehyde.

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