Nucleic acids Knowledge-Based Practice

Chemistry · Organic Chemistry · Chemistry · Polymers & Biomolecules

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

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Questions

  1. 1.

    Which chemical factor explains why ribonucleic acid (RNA) undergoes rapid degradation under alkaline conditions, whereas deoxyribonucleic acid (DNA) is resistant?

    • A) The basic medium deprotonates uracil rings, generating electrostatic repulsions that dissociate the backbone.
    • B) The phosphodiester linkages in RNA possess lower intrinsic resonance stabilization than those in DNA.
    • C) The N-glycosidic bonds linking ribose to the nitrogenous bases undergo base-catalyzed hydrolysis.
    • D) The 2'-hydroxyl group of ribose acts as an intramolecular nucleophile that attacks the adjacent phosphodiester bridge.
  2. 2.

    In the chemical structure of a nucleoside or nucleotide, which type of covalent linkage connects the nitrogenous base to the pentose sugar unit?

    • A) A β\beta-N-glycosidic bond between the C1' carbon of the pentose and a nitrogen atom of the base
    • B) A phosphoester bond between the C5' carbon of the pentose and an exocyclic amino nitrogen of the base
    • C) An α\alpha-O-glycosidic bond between the C2' carbon of the pentose and an oxygen atom of the base
    • D) An amide linkage between the C3' carbon of the pentose and a ring carbonyl group of the base
  3. 3.

    Which of the following nitrogenous bases possesses a bicyclic purine ring system and forms three hydrogen bonds with its complementary base in double-stranded DNA?

    • A) Cytosine
    • B) Thymine
    • C) Guanine
    • D) Uracil
  4. 4.

    In nucleic acid chemistry, which structural feature distinguishes the pentose sugar unit of ribonucleic acid (RNA) from that of deoxyribonucleic acid (DNA)?

    • A) The attachment of an extra hydroxyl group at the 1' position
    • B) The absence of the primary alcohol group at the 5' position
    • C) The loss of the secondary hydroxyl group at the 3' position
    • D) The presence of a hydroxyl group at the 2' position instead of a hydrogen atom
  5. 5.

    Which of the following describes the repeating covalent linkage that joins individual nucleotide monomers together in the backbone of a nucleic acid chain?

    • A) An amide bond connecting an amino group on one nitrogenous base to a carboxyl group on an adjacent base
    • B) An N-glycosidic bond linking carbon-1 of one pentose sugar directly to carbon-4 of the neighboring pentose ring
    • C) A phosphodiester bond connecting the 3'-carbon of one pentose sugar to the 5'-carbon of the adjacent sugar via a phosphate group
    • D) An ether linkage formed by the condensation of hydroxyl groups at the 2'-positions of adjacent ribonucleotide units

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