Chapter 29: 31P (page 1192)
Devise a synthesis of the following dipeptide from amino acid starting materials.
Chapter 29: 31P (page 1192)
Devise a synthesis of the following dipeptide from amino acid starting materials.
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Get started for freeDraw the organic products formed in each reaction.
a.
b.
c.
d.
e.
f.
Histidine is classified as a basic amino acid because one of the N atoms in its five-membered ring is readily protonated by acid. Which N atom in histidine is protonated and why?
Give the amino acid sequence of each peptide using the fragments obtained by partial hydrolysis of the peptide with acid.
Use the given experimental data to deduce the sequence of an octapeptide that contains the following amino acids: Ala, Gly (2 equiv), His (2 equiv), Ile, Leu and Phe. Edman degradation cleaves Gly from the octapeptide, and carboxypeptidase forms Leu and a heptapeptide. Partial hydrolysis forms the following fragments: Ile-His-Leu, Gly, Gly-Ala-Phe-His, and Phe-His-Ile.
What form exists at the isoelectric point of each of the following amino acids: (a) valine; (b)leucine; (c)proline; (d) glutamic acid
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