Chapter 21: Q36P-a (page 1129)

Show how you would accomplish the following synthetic transformations. You may use any necessary reagents. $(a) N - ethylbenzamide \to benzylethylamine$

Short Answer

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Synthetic transformation for N-ethylbenzamide to benzylethylamine is show as,

Step by step solution

Step-by-Step SolutionStep 1: Use of LiAIH4reagent

${LiAIH}_{4}$ is a strong reducing agent for polar double bonds, as it easily thought of as a source of $H^{-}$ . It will reduce aldehydes, ketones,esters, carboxylic acid chloride, carboxylic acids and even carboxylate salts to alcohols.

${LiAIH}_{4}$ is also reduce the amide and nitriles to amine, In above reaction amide is reduce to amine.

Synthesis of benzylethylamine from N-ethylbenzamide

When N-ethylbenzamide react with ${LiAIH}_{4}$ and $H_{2} O$ then there is a formation of benzylethylamine, in this reaction carbonyl group are direct reduce to alkane.

Formation of benzylethylamine

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Show how you would accomplish the following synthetic transformations. You may use any necessary reagents. $(a) N - ethylbenzamide \to benzylethylamine$

Short Answer

Step by step solution

Step-by-Step SolutionStep 1: Use of LiAIH4reagent

Synthesis of benzylethylamine from N-ethylbenzamide

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Show how you would accomplish the following synthetic transformations. You may use any necessary reagents.(a)N-ethylbenzamide→benzylethylamine

Short Answer

Step by step solution

Step-by-Step SolutionStep 1: Use of LiAIH4reagent

Synthesis of benzylethylamine from N-ethylbenzamide

One App. One Place for Learning.

Most popular questions from this chapter

Recommended explanations on Chemistry Textbooks

Kinetics

Nuclear Chemistry

The Earths Atmosphere

Organic Chemistry

Ionic and Molecular Compounds

Physical Chemistry

Study anywhere. Anytime. Across all devices.

Show how you would accomplish the following synthetic transformations. You may use any necessary reagents. $(a) N - ethylbenzamide \to benzylethylamine$