Join thousands of students who trust us to help them ace their exams!Watch the first video
Multiple Choice
Which of the following functional groups of an amino acid would be in the ionized (deprotonated) state at high pH?
A
Amino group (\(-NH_2\))
B
Side chain of glycine
C
Hydrogen atom attached to the alpha carbon
D
Carboxyl group (\(-COO^-\))
Verified step by step guidance
1
Understand the concept of pH and its effect on ionization: At high pH (basic conditions), the environment has a low concentration of hydrogen ions ( ext{H}^+), which promotes deprotonation of acidic functional groups.
Identify the functional groups in an amino acid: Amino acids typically have an amino group ( ext{-NH}_2), a carboxyl group ( ext{-COOH}), a hydrogen atom attached to the alpha carbon, and a side chain (R group).
Determine the behavior of the carboxyl group ( ext{-COOH}) at high pH: The carboxyl group is acidic and tends to lose a proton ( ext{H}^+) under basic conditions, becoming ionized as ext{-COO}^-.
Analyze the amino group ( ext{-NH}_2): The amino group is basic and tends to accept a proton ( ext{H}^+) under acidic conditions, but at high pH, it remains in its neutral state ( ext{-NH}_2) and does not ionize further.
Conclude that the carboxyl group ( ext{-COO}^-) is the functional group that would be in the ionized (deprotonated) state at high pH, as it loses a proton and becomes negatively charged.