Amides Knowledge-Based Practice

Chemistry · Organic Chemistry · Chemistry · Functional Groups

5 Chemistry practice questions on Amides. Questions that assess core concepts and understanding.

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Questions

  1. 1.

    Which of the following organic compounds is formed as the major product when butanamide is heated in the presence of phosphorus pentoxide (P4O10\text{P}_4\text{O}_{10})?

    • A) Butan-1-amine
    • B) Butanoic acid
    • C) Butanenitrile
    • D) Butanal
  2. 2.

    Which of the following organic compounds is formed when propanamide is treated with lithium aluminium hydride (LiAlH4\text{LiAlH}_4) in dry ether, followed by aqueous workup?

    • A) Propan-1-ol
    • B) Propan-1-amine
    • C) Propanoic acid
    • D) Propanenitrile
  3. 3.

    Which of the following pairs of products is obtained from the complete acidic hydrolysis of N-methylpropanamide with aqueous hydrochloric acid?

    • A) Propanoic acid and methanol
    • B) Propanoic acid and methylammonium chloride
    • C) Propan-1-ol and methanamide
    • D) Propanoate ion and methylamine
  4. 4.

    Which of the following nitrogen-containing compounds reacts with an acyl chloride to yield a tertiary amide as the major organic product?

    • A) Ammonia
    • B) A primary amine
    • C) A secondary amine
    • D) A tertiary amine
  5. 5.

    Which of the following statements correctly explains why amides are significantly less basic than aliphatic amines?

    • A) The lone pair of electrons on the amide nitrogen is delocalized into the adjacent carbonyl π\pi system through resonance.
    • B) The amide nitrogen possesses a rigid tetrahedral geometry that physically shields its lone pair from incoming protons.
    • C) The adjacent carbonyl oxygen atom donates electron density to the nitrogen atom through strong inductive effects.
    • D) The nitrogen atom in an amide lacks a nonbonding electron pair because it participates in permanent triple bonding.

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