- 28.28.1: aw the other three stereoisomers of L-isoleucine, and label the ste...
- 28.28.2: What form exists at the isoelectric point of each of the following ...
- 28.28.3: Explain why the pKa of the NH3 + group of an -amino acid is lower t...
- 28.28.4: What -halo carbonyl compound is needed to synthesize each amino aci...
- 28.28.5: The enolate derived from diethyl acetamidomalonate is treated with ...
- 28.28.6: What amino acid is formed when CH3CONHCH(CO2Et)2 is treated with th...
- 28.28.7: What aldehyde is needed to synthesize each amino acid by the Streck...
- 28.28.8: Draw the products of each reaction. a. large excess NH3 BrCH2COOH c...
- 28.28.9: Which of the following amines can be used to resolve a racemic mixt...
- 28.28.11: Draw the organic products formed in the following reaction. CH2CH(C...
- 28.28.12: What alkene is needed to synthesize each amino acid by an enantiose...
- 28.28.13: Draw the structure of each peptide. Label the N-terminal and C-term...
- 28.28.14: Name each peptide using both the one-letter and the three-letter ab...
- 28.28.15: How many different tripeptides can be formed from three different a...
- 28.28.16: Draw the s-cis and s-trans conformations for the dipeptide formed f...
- 28.28.17: Draw the structure of leu-enkephalin, a pentapeptide that acts as a...
- 28.28.18: Glutathione, a powerful antioxidant that destroys harmful oxidizing...
- 28.28.19: Draw the structure of the N-phenylthiohydantoin formed by initial E...
- 28.28.21: (a) What products are formed when each peptide is treated with tryp...
- 28.28.22: Deduce the sequence of a heptapeptide that contains the amino acids...
- 28.28.23: Devise a synthesis of each peptide from amino acid starting materia...
- 28.28.24: Outline the steps needed to synthesize the tetrapeptide AlaLeuIleGl...
- 28.28.25: Suggest a reason why antiparallel -pleated sheets are generally mor...
- 28.28.26: Consider two molecules of a tetrapeptide composed of only alanine r...
- 28.28.27: What types of stabilizing interactions exist between each of the fo...
- 28.28.28: The fi broin proteins found in silk fi bers consist of large region...
- 28.28.29: Explain why L-alanine has the S confi guration but L-cysteine has t...
- 28.28.31: Explain why amino acids are insoluble in diethyl ether but N-acetyl...
- 28.28.32: Histidine is classifi ed as a basic amino acid because one of the N...
- 28.28.33: Tryptophan is not classifi ed as a basic amino acid even though it ...
- 28.28.34: What is the structure of each amino acid at its isoelectric point: ...
- 28.28.35: To calculate the isoelectric point of amino acids having other ioni...
- 28.28.36: What is the predominant form of each of the following amino acids a...
- 28.28.37: What is the predominant form of each of the following amino acids a...
- 28.28.38: a. Draw the structure of the tripeptide AAA, and label the two ioni...
- 28.28.39: Draw the organic product formed when the amino acid leucine is trea...
- 28.28.41: Draw the organic products formed in each reaction. a. (CH3)2CHCH2CH...
- 28.28.42: What alkyl halide is needed to synthesize each amino acid from diet...
- 28.28.43: Devise a synthesis of threonine from diethyl acetamidomalonate.
- 28.28.44: Devise a synthesis of each amino acid from acetaldehyde (CH3CHO): (...
- 28.28.45: Identify the lettered intermediates in the following reaction schem...
- 28.28.46: Glutamic acid is synthesized by the following reaction sequence. Dr...
- 28.28.47: Write out a scheme for the resolution of the two enantiomers of rac...
- 28.28.48: Another strategy used to resolve amino acids involves converting th...
- 28.28.49: Brucine is a poisonous alkaloid obtained from Strychnos nux vomica,...
- 28.28.51: What two steps are needed to convert A to L-dopa, an uncommon amino...
- 28.28.52: Draw the structure for each peptide: (a) PheAla; (b) GlyGln; (c) Ly...
- 28.28.53: For each tetrapeptide [1] AlaGlnCysSer; [2] AspArgValTyr: a. Name t...
- 28.28.54: Name each peptide using both the three-letter and one-letter abbrev...
- 28.28.55: Explain why a peptide C N bond is stronger than an ester C O bond.
- 28.28.56: Draw the s-trans and s-cis conformations of the peptide bond in the...
- 28.28.57: Draw the amino acids and peptide fragments formed when the decapept...
- 28.28.58: Give the amino acid sequence of each peptide using the fragments ob...
- 28.28.59: Angiotensin is an octapeptide that narrows blood vessels, thereby i...
- 28.28.61: An octapeptide contains the following amino acids: Arg, Glu, His, I...
- 28.28.62: Draw all the products formed in the following reaction. C H H OH C ...
- 28.28.63: Draw the organic products formed in each reaction. a. C H CH(CH3)2 ...
- 28.28.64: Draw all the steps in the synthesis of each peptide from individual...
- 28.28.65: Write out the steps for the synthesis of each peptide using the Mer...
- 28.28.66: An amino acid [RCH(NH2)COOH] can readily be converted to an N-acety...
- 28.28.67: Another method to form a peptide bond involves a two-step process: ...
- 28.28.68: In addition to forming an Fmoc-protected amino acid using FmocCl, a...
- 28.28.69: Many different insoluble polymers, called resins, are currently ava...
- 28.28.71: After the peptide chain of collagen has been formed, many of the pr...
- 28.28.72: Devise a stepwise synthesis of the tripeptide ValLeuVal from 3-meth...
- 28.28.73: Besides asymmetric hydrogenation (Section 28.4), several other meth...
- 28.28.74: As shown in Mechanism 28.2, the fi nal steps in the Edman degradati...
Solutions for Chapter 28: Amino Acids and Proteins
Full solutions for Organic Chemistry | 3rd Edition
ISBN: 9780077354725
This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by and is associated to the ISBN: 9780077354725. Since 67 problems in chapter 28: Amino Acids and Proteins have been answered, more than 221275 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 3. Chapter 28: Amino Acids and Proteins includes 67 full step-by-step solutions.
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Anion
An atom or group of atoms bearing a negative charge.
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Atropisomers
Enantiomers that lack a chiral center and differ because of hindered rotation.
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Avogadro’s law.
At constant pressure and temperature, the volume of a gas is directly proportional to the number of moles of the gas present. (5.3)
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cathode rays
Streams of electrons that are produced when a high voltage is applied to electrodes in an evacuated tube. (Section 2.2)
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Constitutional isomers
Compounds with the same molecular formula but a different connectivity of their atoms
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critical pressure (Pc).
The minimum pressure necessary to bring about liquefaction at the critical temperature. (11.8)
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crossed Claisen condensation
A Claisen condensation reaction that occurs between different partners.
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Diastereomers
Stereoisomers that are not mirror images of each other; refers to relationships among two or more objects
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Diels-Alder adduct
A cyclohexene resulting from the cycloaddition reaction of a diene and a dienophile.
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Diol
A compound containing two hydroxyl groups
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flagpole interactions
For cyclohexane, the steric interactions that occur between the flagpole hydrogen atoms in a boat conformation.
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heterogeneous catalyst
A catalyst that does not dissolve in the reaction medium.
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N terminus
For a peptide chain,the end that contains the amino group.
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oxyacid
A compound in which one or more OH groups, and possibly additional oxygen atoms, are bonded to a central atom. (Section 16.10)
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partially condensed structures
A drawing style in which the CH bonds are not drawn explicitly, but all other bonds are drawn.
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peptide
A chain comprised of a small number of amino acid residues.
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Resonance hybrid
A molecule, ion, or radical described as a composite of a number of contributing structures
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secondary cell
A voltaic cell that can be recharged. (Section 20.7)
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systematic name
A name that is assigned using the rules of IUPAC nomenclature.
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Wohl degradation
A process that involves the removal of a carbon atom from an aldose. The aldehyde group is first converted to a cyanohydrin, followed by loss of HCN in the presence of a base.