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.
Report an error
The more specific you are, the faster it gets fixed. A source beats an opinion.
Prefer email? [email protected]
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.
Practise Alkyl Halides
458 free Alkyl Halides MCQs from Chemistry, each with the correct answer and an explanation. Unlimited attempts, no account needed.
Discussion
Stuck on an option, or know a faster way to get there? Ask or explain it here.
No comments yet. Be the first to explain this one.
Exams that ask Chemistry questions like this
Chemistry is on 14 papers prepared for on TestUstad, and all of them draw the same bank, so this question is worth knowing for every one of them.
More Nucleophilic Substitution questions
Which of the following base will favour substitution reaction as compared to the elimination reaction?
Example of a nucleophile is:
When methl iodide and ethyl iodide are treated with sodium metal possible major products are obtained ?
Propose which one of the following reactions is more likely to occur through SN1 mechanism?
A compound X undergoes the following reactions:X NaOH(aq)/heat > C4H10O Cr2O7(2-), H+(aq)/ heat> C4H8O.What is X?
What is true about the mechanisms I and II