Chapter 24: Q12P (page 1270)
Show how you would use a Strecker synthesis to make
- Leucine (b) Valine (c) Aspartic acid
Answer
Short Answer
(a)
Formation of leucine
(b)
Formation of valine
(c)
Formation of aspartic acid
Chapter 24: Q12P (page 1270)
Show how you would use a Strecker synthesis to make
Answer
(a)
Formation of leucine
(b)
Formation of valine
(c)
Formation of aspartic acid
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Get started for freeThere are many methods for activating a carboxylic acid in preparation for coupling with an amine. The following method converts the acid to an N-hydroxysuccinimide (NHS) ester.
(a) Explain why an NHS ester is much more reactive than a simple alkyl ester.
(b) Propose a mechanism for the reaction shown.
(c) Propose a mechanism for the reaction of the NHS ester with an amine, R-NH2
Draw the resonance forms of a protonated guanidino group and explain why arginine has such a strongly basic isoelectric point.
Draw three-dimensional representation of the following amino acids:
(a) L-alanine
(b) L-Leucine
(c) D-serine
(d) D-glutamine
Write the complete structures for the following peptides. Tell whether each peptide is acidic, basic, or neutral.
Question: Propose a mechanism for the acid-catalyzed hydrolysis of phenylalanine ethyl ester.
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