Asked by Jwalanda Pariyar on Sep 24, 2024

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Lithium aluminum hydride reduces carboxylic acids to primary alcohols via what intermediate?

A) a ketone
B) a methyl ester
C) an aldehyde
D) a secondary alcohol
E) an acid chloride

Primary Alcohols

Organic compounds featuring a hydroxyl group (-OH) attached to a primary carbon atom, often reactive and used in the production of various chemicals and solvents.

Carboxylic Acids

Organic compounds characterized by the presence of at least one carboxyl group (-COOH), which includes substances like acetic acid and butyric acid.

Lithium Aluminum Hydride

A powerful reducing agent used in organic synthesis to reduce esters, carboxylic acids, and amides to alcohols.

  • Recognize the reagents and conditions necessary for specific organic transformations.
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Verified Answer

DN
Diana Nguyenabout 19 hours ago
Final Answer :
C
Explanation :
Lithium aluminum hydride reduces carboxylic acids to aldehydes, which are then further reduced to primary alcohols.