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Mutarotation of glucose is best explained as the:

Answer: Interconversion of the alpha- and beta-anomers.

  • A Interconversion of the alpha- and beta-anomers
  • B Oxidation of glucose to gluconic acid
  • C Rotation of the whole molecule in water
  • D Formation of an osazone derivative

Correct answer: A. Interconversion of the alpha- and beta-anomers

Explanation: Mutarotation is the gradual change in specific rotation as alpha-D-glucose and beta-D-glucose interconvert through the open-chain form until equilibrium is reached.

Peptide Bond Formation (Condensation)H₂N-CH(R₁)-C(=O)OHAmino acid 1+HNH-CH(R₂)-COOHAmino acid 2H₂N-CH(R₁)-CO-NH-CH(R₂)-COOHDipeptide+ H₂OThe -OH (from acid 1) and -H (from amine 2) combine to release water, forming the -CO-NH- peptide bond

Two amino acids join via a condensation reaction: the carboxyl -OH of one and an amine -H of the other are eliminated as water, leaving a peptide bond (-CO-NH-) linking them into a dipeptide; repeating this builds a full protein chain.

Concept context

The chemistry of life: carbohydrates, proteins, lipids, nucleic acids, enzymes, and vitamins. Understand their structures, classification, and biological functions. Highly relevant for NEET and Class 12 board exams.

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