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🧪 Chemistry  ·  Biomolecules  ·  NEET & JEE

Zwitterion formation in amino acids occurs because:

Answer: The amino group accepts a proton from the carboxyl group intramolecularly.

  • A The amino group accepts a proton from the carboxyl group intramolecularly
  • B An external acid molecule donates a proton to the amino group in standard practice
  • C The hydrophobic R group ionises under physiological pH under most conditions encountered
  • D Surrounding water molecules donate protons to both ends as frequently observed in practice

Correct answer: A. The amino group accepts a proton from the carboxyl group intramolecularly

Explanation: In a zwitterion, the -COOH donates a proton to the -NH<sub>2</sub> group, giving -COO- and -NH<sub>3</sub><sup>+</sup>.

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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