Question
Consider the following reaction: The product 'A' is:
C6H5OH
C6H5COCH3
C6H5Cl
C6H5CHO
Based on the AIPMT 2012 context and the options provided, the reaction refers to the preparation of benzaldehyde (). A common name reaction appearing in this exam yielding benzaldehyde is the Rosenmund Reduction, where benzoyl chloride () is hydrogenated over a catalyst of palladium on barium sulphate () poisoned with sulphur or quinoline.
Other possibilities include the Etard Reaction (oxidation of toluene with chromyl chloride) or Gattermann-Koch reaction (benzene with CO/HCl), both of which also yield benzaldehyde [1]. The product 'A' is Benzaldehyde.
This question aligns with the NEET CHEMISTRY syllabus, specifically targeting concepts from Aldehydes, Ketones and Carboxylic Acids. Mastering this topic is crucial for scoring well in the upcoming medical entrance examinations. Solving conceptually related problems will help you understand the nuances of these concepts and improve your problem-solving speed.
More Aldehydes, Ketones and Carboxylic Acids Questions
The product formed from the following reaction sequence is:
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The intermediate compound 'X' in the following chemical reaction is: $$\text{Toluene} \xrightarrow{CrO_2Cl_2/CS_2} X \xrightarrow{H_3O^+} \text{Benzaldehyde}$$
The product that cannot be formed in the following reaction is:
The correct statement regarding a carbonyl compound with a hydrogen atom on its alpha-carbon is:
The product of the below-mentioned reaction is: (Reaction Scheme Missing)
$$RMgX + CO_2 \xrightarrow{\text{dry ether}} Y \xrightarrow{H_3O^+} RCOOH$$ What is Y in the above reaction?
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