Chapter 29: 29P (page 1191)
Draw the product formed when the following amino acid is treated with each reagent: (a); (b), pyridine; (c) HCl (1 equiv); (d) NaOH (1 equiv); (e).
Chapter 29: 29P (page 1191)
Draw the product formed when the following amino acid is treated with each reagent: (a); (b), pyridine; (c) HCl (1 equiv); (d) NaOH (1 equiv); (e).
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Get started for freeUse 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 aldehyde is needed to synthesize each amino acid by the Strecker synthesis?
(a) Valine;
(b) Leucine;
(c) Phenylalanine.
Name each peptide using both the three-letter and one-letter abbreviations of the component amino acids.
a.
b.
The enolate derived from diethyl acetamidomalonate is treated with each of the following alkyl halides. After hydrolysis and decarboxylation, what amino acid is formed?
a. CH3I
b. (CH3)2CHCH2Cl
c. CH3CH2CH(CH3)Br
What is the predominant form of each of the following amino acids at pH=11? What is the overall charge on the amino acid? (a)valine; (b)proline; (c)glutamic acid; (d)lysine?
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