BIO NMDCAT Carbohydrates
nmdcat.online June 27, 2026

In the formation of a ring structure, the reaction between the carbonyl group and a hydroxyl group of a monosaccharide creates a more reactive form known as a

A. Enantiomer
B. Hemiacetal or hemiketal
C. Epimer
D. Zwitterion

📝 Explanation

The nucleophilic addition of an alcohol (hydroxyl group) to a carbonyl group forms a hemiacetal (from an aldehyde) or a hemiketal (from a ketone). This intramolecular reaction converts the linear monosaccharide into its cyclic form, creating a new chiral center (the anomeric carbon).

📖 Additional Information

  • Enantiomer
  • Hemiacetal or hemiketal
  • Epimer
  • Zwitterion

The nucleophilic addition of an alcohol (hydroxyl group) to a carbonyl group forms a hemiacetal (from an aldehyde) or a hemiketal (from a ketone). This intramolecular reaction converts the linear monosaccharide into its cyclic form, creating a new chiral center (the anomeric carbon).

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