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Return to An Introduction to Drug Synthesis 1e Student Resources
Chapter 14 Multiple Choice Questions
Quiz Content
*
not completed
.
Which of the following diagrams has the correct numbering system for fluoroquinolones?
Diagram A
correct
incorrect
Diagram B
correct
incorrect
Diagram C
correct
incorrect
Diagram D
correct
incorrect
*
not completed
.
Which of the following was the first therapeutically useful quinolone antibaterial agent?
Ciprofloxacin
correct
incorrect
Enoxacin
correct
incorrect
Ofloxacin
correct
incorrect
Nalidixic acid
correct
incorrect
*
not completed
.
Which of the following structures is ciprofloxacin?
Structure A
correct
incorrect
Structure B
correct
incorrect
Structure C
correct
incorrect
Structure D
correct
incorrect
*
not completed
.
Which enzymes are the target for the quinolone antibacterial agents?
Topoisomerases
correct
incorrect
Kinases
correct
incorrect
Proteases
correct
incorrect
Transpeptidases
correct
incorrect
*
not completed
.
Which amino acid residue in topoisomerases is responsible for the temporary splitting of DNA strands?
Phenylalanine
correct
incorrect
Tyrosine
correct
incorrect
Serine
correct
incorrect
Aspartate
correct
incorrect
*
not completed
.
Which region of the fluoroquinolone skeleton is involved in binding interactions with DNA in the ternary complex formed between DNA, toposiomerase and the drug?
Region A
correct
incorrect
Region B
correct
incorrect
Region C
correct
incorrect
Region D
correct
incorrect
*
not completed
.
Which of the following fluoroquinolones is chiral?
Structure A
correct
incorrect
Structure B
correct
incorrect
Structure C
correct
incorrect
Structure D
correct
incorrect
*
not completed
.
Which of the following structures would be a feasible intermediate for the synthesis of fluoroquinolones having antibacterial activity?
Structure A
correct
incorrect
Structure B
correct
incorrect
Structure C
correct
incorrect
Structure D
correct
incorrect
*
not completed
.
Gatifloxacin has been synthesised using a strategy where an intramolecular cyclisation was carried out that involved nucleophilic substitution of an aryl halide.
Which of the structures (A-D) would be suitable as the staring material for this synthesis?
Structure A
correct
incorrect
Structure B
correct
incorrect
Structure C
correct
incorrect
Structure D
correct
incorrect
*
not completed
.
The synthesis of clinafloxacin includes the following reaction.
Which of the substituents present in the starting material is likely to have the greatest influence over the regioselectiivity of the reaction?
The fluorine substituent (A)
correct
incorrect
The chlorine substituent (B)
correct
incorrect
The carbonyl group (C)
correct
incorrect
The nitrogen atom (D)
correct
incorrect
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