Question 1

How does acid-catalyzed hydrolysis convert nitriles to carboxylic acids?

Accepted Answer

In acid-catalyzed hydrolysis, the nitrile nitrogen is first protonated, making the cyano carbon more electrophilic. Water then attacks this activated carbon. The resulting imidic acid tautomerizes to an amide through protonation and deprotonation steps. Finally, the amide undergoes multi-step hydrolysis to generate the carboxylic acid product.

Question 2

What is the difference between acid-catalyzed and base-catalyzed nitrile hydrolysis?

Accepted Answer

Acid-catalyzed hydrolysis produces carboxylic acids through an imidic acid intermediate and amide formation. Base-catalyzed hydrolysis directly generates carboxylate anions instead. Both pathways convert nitriles to carboxylic acid products, but base conditions yield the deprotonated carboxylate form rather than the protonated acid.

Question 3

How are haloalkanes converted to carboxylic acids using nitriles?

Accepted Answer

Haloalkanes are first converted to nitriles via SN2 reaction with sodium cyanide, introducing one additional carbon. The resulting nitrile is then hydrolyzed under aqueous acidic or basic conditions to yield carboxylic acids. This two-step process effectively extends the carbon chain while converting the halide to a carboxylic acid functional group.

Question 4

What solvents are used in nitrile hydrolysis reactions?

Accepted Answer

Nitrile hydrolysis reactions use dimethyl sulfoxide, alcohols, or water as solvents to facilitate the aqueous hydrolysis conditions necessary for converting nitriles to carboxylic acids. The choice of solvent depends on reaction conditions and substrate compatibility. These solvents enable efficient nucleophilic attack and product formation.

Question 5

Why are tertiary alkyl halides rarely used in nitrile synthesis for carboxylic acid preparation?

Accepted Answer

Tertiary alkyl halides are seldom used because the nitrile synthesis step relies on the SN2 mechanism, which requires nucleophilic attack at a primary or secondary carbon. Tertiary carbons are sterically hindered and favor SN1 pathways instead, making them unsuitable for efficient nitrile formation and subsequent carboxylic acid synthesis.

Question 6

What is the role of the imidic acid intermediate in acid-catalyzed nitrile hydrolysis?

Accepted Answer

The imidic acid is a key intermediate formed after water attacks the protonated nitrile. It tautomerizes to a more stable amide form through protonation of the imidic nitrogen, creating a resonance-stabilized protonated amide. Subsequent deprotonation yields the amide, which then undergoes hydrolysis to form the final carboxylic acid.

Question 7

How is ibuprofen synthesized using nitrile hydrolysis?

Accepted Answer

Ibuprofen is synthesized via nitrile formation followed by base-catalyzed hydrolysis. The nitrile intermediate is generated from a haloalkane precursor, then hydrolyzed under basic aqueous conditions to produce the carboxylic acid component of ibuprofen. This demonstrates the practical application of nitrile hydrolysis in pharmaceutical synthesis.

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