Identify the product formed when benzoyl chloride is reduced by hydrogen using a palladium catalyst poisoned with barium sulphate.

  • A
    Chlorobenzene
  • B
    Benzyl alcohol
  • C
    Benzene
  • D
    Benzaldehyde

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Similar Questions

Consider the following statements. Acetophenone can be prepared by:
$1$. Oxidation of $1$-phenylethanol
$2$. Reaction of benzaldehyde with methyl magnesium bromide
$3$. Friedel-Crafts reaction of benzene with acetyl chloride
$4$. Distillation of calcium benzoate

Ethylbenzene is generally prepared by acetylation of benzene followed by reduction and not by direct alkylation. Explain why.

Which of the following reactions uses $SnCl_2/HCl$ as a catalyst?

Which of the following methods can be used to prepare acetophenone?

The reagents used in the Etard reaction $(I)$ and the Stephen reaction $(II)$ are:

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