Chapter 29: Q37. (page 1192)
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?
Chapter 29: Q37. (page 1192)
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?
All the tools & learning materials you need for study success - in one app.
Get started for freeDevise a synthesis of threonine from diethyl acetamidomalonate.
Another method to form a peptide bond involves a two-step process:
[1] Conversion of a Boc-protected amino acid to a p-nitrophenyl ester.
[2] Reaction of the p-nitrophenyl ester with an amino acid ester.
Why does a p-nitrophenyl ester “activate” the carboxy group of the first amino acid to amide formation?
Would a p-methoxyphenyl ester perform the same function? Why or why not?
Outline the steps needed to synthesize the tetrapeptideAla–Leu–Ile–Gly using the Merrifield technique.
Question: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).
What amino acid is formed whenis treated with the following series of reagents:
role="math" localid="1648630585393"
What do you think about this solution?
We value your feedback to improve our textbook solutions.