Chapter 29: Q62. (page 1196)
Write out the steps for the synthesis of each peptide using the Merrifield method:
- Ala-Leu-Phe-Phe; (b) Phe-Gly-Ala-Ile.
Chapter 29: Q62. (page 1196)
Write out the steps for the synthesis of each peptide using the Merrifield method:
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Get started for freeQuestion: Identify the functional groups in each molecule. Classify each alcohol, alkyl halide, amide, and amine as 1°, 2°, or 3°
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b.
c.
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e.
f.
Which of the following amines can be used to resolve a racemic mixture of amino acids?
(a)
(b)
(c)
(d)
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.
Question: Into how many peaks will each proton shown in green be split?
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b.
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e.
Image Caption
f.
Devise a synthesis of each peptide from amino acid starting materials: (a) Leu–Val; (b) Ala–Ile–Gly.
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