Chapter 27: Problem 14
Why are Glu and Asp often referred to as acidic amino acids?
Chapter 27: Problem 14
Why are Glu and Asp often referred to as acidic amino acids?
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Get started for freeThe side-chain carboxyl groups of aspartic acid and glutamic acid are often protected as benzyl esters. (a) Show how to convert the side-chain carboxyl group to a benzyl ester using benzyl chloride as a source of the benzyl group. (b) How do you deprotect the side-chain carboxyl under mild conditions without removing the \(B O C\)-protecting group at the same time?
Distinguish between intermolecular and intramolecular hydrogen bonding between the backbone groups on polypeptide chains. In what type of secondary structure do you find intermolecular hydrogen bonds? In what type do you find intramolecular hydrogen bonding?
Describe the behavior of a mixture of glutamic acid, arginine, and valine on paper electrophoresis at \(\mathrm{pH} 6.0\).
Write the zwitterion form of alanine and show its reaction with the following. (a) \(1 \mathrm{~mol} \mathrm{NaOH}\) (b) \(1 \mathrm{~mol} \mathrm{HCl}\)
The configuration of the chiral center in \(\alpha\)-amino acids is most commonly specified using the \(\mathrm{D}, \mathrm{L}\) convention. It can also be identified using the \(R, S\) convention (Section 3.3). Does the chiral center in L-serine have the \(R\) or \(S\) configuration?
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