Predict the product of reaction:
Correct answer: B. CH3 - CH2 -NH2
- A. CH3 - NH2
- B. CH3 - CH2 -NH2
- C. OH|CH3 - CH - CH3
- D. O||CH3 - C - OH
Explanation
Ethylamine is the correct product of the reduction of acetamides. Acetamides, when reduced, undergo cleavage of the amide bond to form a primary amine. In this case, the specific primary amine formed is ethylamine.
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About Nucleophilic Substitution
Nucleophilic substitution replaces a leaving group in an alkyl halide when an electron-rich nucleophile attacks the carbon atom. The topic compares SN1 and SN2 mechanisms, including reaction conditions, substrate structure, solvent effects, nucleophile strength, carbocation formation and stereochemical changes, and distinguishes substitution from elimination.
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