Question:medium

 Rosenmund reduction
This reduction reaction is known as:

Updated On: Jan 13, 2026
  • Etard Reaction
  • Stephen's Reaction
  • Wolff Kishner Reduction
  • Rosenmund reduction
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The Correct Option is D

Solution and Explanation

The presented problem depicts a specific chemical reaction requiring its identification.

Concept Used:

The depicted reaction is a named organic chemistry reaction utilized for synthesizing aldehydes. Key indicators for identification include the starting material (acyl chloride), the resultant product (an aldehyde), and the specific reducing agents employed (hydrogen gas in conjunction with a deactivated palladium catalyst).

Rosenmund Reduction: This process involves the catalytic hydrogenation of an acyl chloride to yield an aldehyde. The catalyst typically comprises palladium supported on barium sulfate (\(Pd/BaSO_4\)), often modified with a deactivating agent such as sulfur or quinoline. This deactivation moderates the palladium catalyst's activity, preventing the over-reduction of the aldehyde to a primary alcohol.

\[R-COCl + H_2 \xrightarrow{Pd/BaSO_4} R-CHO + HCl\]

Step-by-Step Solution:

Step 1: Identify the reactant and product.

  • The initial substance is Benzoyl chloride (\(C_6H_5COCl\)), an aromatic acyl chloride.
  • The final compound is Benzaldehyde (\(C_6H_5CHO\)), an aromatic aldehyde.

The overall transformation involves converting the acid chloride moiety (\(-COCl\)) into an aldehyde group (\(-CHO\)).

Step 2: Identify the reaction reagents.

The reagents are hydrogen gas (\(H_2\)) and a catalyst consisting of Palladium on Barium Sulfate (\(Pd-BaSO_4\)).

Step 3: Correlate the transformation and reagents with a named reaction.

The catalytic reduction of an acyl chloride to an aldehyde using hydrogen gas over a deactivated palladium catalyst (e.g., \(Pd-BaSO_4\)) constitutes a distinct and recognized named reaction.

Within this catalytic system:

  • Palladium (Pd) functions as the hydrogenation catalyst.
  • Barium Sulfate (BaSO₄) offers an extensive surface area for the catalyst and, critically, acts as a catalyst poison, diminishing its activity.

This controlled reduction, which ceases at the aldehyde stage and avoids progression to the alcohol, is characteristic of the Rosenmund Reduction.

Final Computation & Result:

Based on the examination of the reactant, product, and the specific catalytic system employed, the reaction presented is a textbook instance of the Rosenmund reduction.

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