EP FUND.OF GENERAL,ORG...-MOD.MASTERING
8th Edition
ISBN: 9780134326061
Author: McMurry
Publisher: PEARSON CO
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Textbook Question
Chapter 10, Problem 10.40AP
What happens when a strong base such as KOH solved in water?
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The carbon-nitrogen peptide bond is rigid, but rotation can take place
about the bond between the nitrogen and a-carbon atoms and the bond
between the a-carbon and the carbonyl carbon atom. These bond angles
define the conformation of the peptide chain.
Consider the Ramachandran plot shown to answer both questions.
fr (degrees)
180
120
8280
60
°
-60
Which observation most likely describes part of an observed a helix?
p=-59 degrees; y = +150 degrees; many Ser residues
qp=-140 degrees; w +130 degrees; many Val residues
qp=-57 degrees; y = -47 degrees; many Pro residues
qp=-60 degrees; y = -47 degrees; many Ala residues
p = +60 degrees; y = +40 degrees; many Gly residues
Which observations would not likely occur in a ẞ sheet?
qp=-59 degrees; y = -49 degrees; many Ala residues
qp = +60 degrees; w = +60 degrees; many Gly residues
qp=-120 degrees; y = +120 degrees; many Tyr residues
☐ ☐
qp=-139 degrees; y = +135 degrees; many Val residues
op=-51 degrees; w+153 degrees; many Gly and Pro…
Please give an intuitive explanation of the difference, if any, between toxicokinetics and pharmacokinetics.
A protein biochemist attempted to determine the amino acid sequence of a decapeptide. The results from the trypsin,
chymotrypsin, and cyanogen bromide treatments are shown:
⚫ Trypsin digestion gave two fragments with multiple residues (not in order):
• T1: Ala, Arg, Phe, Gly, Thr, Trp, Tyr
o T2: Lys, Met, Val
Chymotrypsin digestion gave four fragments with multiple residues (not in order):
• CT1: Ala, Phe
• CT2: Thr, Trp
• CT3: Lys, Met, Tyr, Val
。 CT4: Arg, Gly
⚫ Treatment with cyanogen bromide yielded a single amino acid, methionine, and a nonapeptide.
What is a possible sequence of the decapeptide? Use three-letter abbreviations in your answer, and add a dash between
each residue.
Chapter 10 Solutions
EP FUND.OF GENERAL,ORG...-MOD.MASTERING
Ch. 10.1 - Which of the following are BrnstedLowry acids?...Ch. 10.1 - Prob. 10.2PCh. 10.1 - Prob. 10.3PCh. 10.1 - Prob. 10.4KCPCh. 10.2 - The concentration of HCl when released to the...Ch. 10.2 - Prob. 10.2CIAPCh. 10.2 - Prob. 10.3CIAPCh. 10.2 - Prob. 10.5PCh. 10.2 - Prob. 10.6PCh. 10.2 - Prob. 10.7P
Ch. 10.2 - Prob. 10.8PCh. 10.2 - Prob. 10.9KCPCh. 10.3 - Prob. 10.10PCh. 10.4 - Prob. 10.11PCh. 10.5 - Prob. 10.12PCh. 10.5 - Prob. 10.13PCh. 10.5 - Prob. 10.14PCh. 10.6 - Identify the following solutions as acidic or...Ch. 10.6 - Calculate the pH of the following solutions and...Ch. 10.6 - What is the pH of a 0.0025 M solution of HCl?Ch. 10.6 - Prob. 10.4CIAPCh. 10.6 - Prob. 10.5CIAPCh. 10.7 - How many equivalents are in the following? (a) 5.0...Ch. 10.7 - Prob. 10.19PCh. 10.8 - Maalox, an over-the-counter antacid, contains...Ch. 10.8 - Prob. 10.21PCh. 10.8 - Prob. 10.22PCh. 10.8 - Show how ethylamine (C2H5NH2) reacts with...Ch. 10.9 - Predict whether the following salts produce an...Ch. 10.10 - What is the pH of 1.00 L of the 0.100 M...Ch. 10.10 - Prob. 10.26PCh. 10.10 - Prob. 10.27PCh. 10.10 - A buffer solution is prepared using CN-(from NaCN...Ch. 10.11 - A titration is carried out to determine the...Ch. 10.11 - Prob. 10.30PCh. 10.11 - Prob. 10.31PCh. 10.11 - Prob. 10.32PCh. 10.11 - Prob. 10.6CIAPCh. 10.11 - Prob. 10.7CIAPCh. 10 - Prob. 10.33UKCCh. 10 - Prob. 10.34UKCCh. 10 - The following pictures represent aqueous acid...Ch. 10 - Prob. 10.36UKCCh. 10 - Prob. 10.37UKCCh. 10 - Prob. 10.38APCh. 10 - What happens when a weak acid such as CH3CO2H is...Ch. 10 - What happens when a strong base such as KOH solved...Ch. 10 - Prob. 10.41APCh. 10 - Prob. 10.42APCh. 10 - Prob. 10.43APCh. 10 - Prob. 10.44APCh. 10 - Prob. 10.45APCh. 10 - Prob. 10.46APCh. 10 - Label the BrnstedLowry acids and bases in the...Ch. 10 - Write the formulas of the conjugate acids of the...Ch. 10 - Write the formulas of the conjugate bases of the...Ch. 10 - Prob. 10.50APCh. 10 - Prob. 10.51APCh. 10 - Prob. 10.52APCh. 10 - Prob. 10.53APCh. 10 - Prob. 10.54APCh. 10 - Write the expressions for the acid dissociation...Ch. 10 - Based on the Ka values in Table 10.3, rank the...Ch. 10 - Prob. 10.57APCh. 10 - A 0.10 M solution of the deadly poison hydrogen...Ch. 10 - Prob. 10.59APCh. 10 - Prob. 10.60APCh. 10 - What is the approximate pH of a 0.02 M solution of...Ch. 10 - Calculate the pOH of each solution in Problems...Ch. 10 - Prob. 10.63APCh. 10 - What are the OH concentration and pOH for each...Ch. 10 - What are the H3O+ and OH concentrations of...Ch. 10 - Prob. 10.66APCh. 10 - Prob. 10.67APCh. 10 - Write balanced equations for proton-transfer...Ch. 10 - Sodium bicarbonate (NaHCO3), also known as baking...Ch. 10 - Refer to Section 10.8 to write balanced equations...Ch. 10 - Prob. 10.71APCh. 10 - For each of the following salts, indicate if the...Ch. 10 - Which salt solutions in problem 10.72 could be...Ch. 10 - Prob. 10.74APCh. 10 - Prob. 10.75APCh. 10 - Prob. 10.76APCh. 10 - Which of the following buffer systems would you...Ch. 10 - What is the pH of a buffer system that contains...Ch. 10 - Consider 1.00 L of the buffer system described in...Ch. 10 - Prob. 10.80APCh. 10 - Prob. 10.81APCh. 10 - Prob. 10.82APCh. 10 - How does normality compare to molarity for...Ch. 10 - Prob. 10.84APCh. 10 - Prob. 10.85APCh. 10 - Prob. 10.86APCh. 10 - Prob. 10.87APCh. 10 - Prob. 10.88APCh. 10 - Prob. 10.89APCh. 10 - Prob. 10.90APCh. 10 - Prob. 10.91APCh. 10 - Titration of a 12.0 mL solution of HCl requires...Ch. 10 - Prob. 10.93APCh. 10 - Titration of a 10.0 mL solution of NH3 requires...Ch. 10 - If 35.0 mL of a 0.100 N acid solution is needed to...Ch. 10 - For the titrations discussed in Problems 10.92 and...Ch. 10 - Prob. 10.97APCh. 10 - Prob. 10.98CPCh. 10 - Prob. 10.99CPCh. 10 - Prob. 10.100CPCh. 10 - Prob. 10.101CPCh. 10 - Prob. 10.102CPCh. 10 - Prob. 10.103CPCh. 10 - Prob. 10.104CPCh. 10 - Prob. 10.105CPCh. 10 - Prob. 10.106CPCh. 10 - Prob. 10.107CPCh. 10 - Prob. 10.108CPCh. 10 - Obtain a package of Alka-Seltzer, an antacid, from...Ch. 10 - Prob. 10.110GPCh. 10 - Prob. 10.111GP
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- A protein biochemist attempted to determine the amino acid sequence of a decapeptide. The results from the trypsin, chymotrypsin, and cyanogen bromide treatments are shown: • Trypsin digestion gave two fragments with multiple residues (not in order): T1: Ala, Arg, Phe, Gly, Thr, Trp, Tyr • T2: Lys, Met, Val Chymotrypsin digestion gave four fragments with multiple residues (not in order): • CTI: Ala, Phe 。 CT2: Thr, Trp • CT3: Lys, Met, Tyr, Val 。 CT4: Arg, Gly ⚫ Treatment with cyanogen bromide yielded a single amino acid, methionine, and a nonapeptide. What is a possible sequence of the decapeptide? Use three-letter abbreviations in your answer, and add a dash between each residue.arrow_forwardPoly-L-leucine in an organic solvent such as dioxane is a helical, whereas poly-L-isoleucine is not. Why do these amino acids with the same number and kinds of atoms have different helix-forming tendencies? L-isoleucine's methyl group sterically interferes with α-helix formation, whereas L-leucine's methyl group does not interfere. L-isoleucine lacks an NH group that can donate a hydrogen bond to stabilize an a helix, whereas L-leucine has an NH group. L-isoleucine contains a hydrogen-bond acceptor in close proximity to the main chain, whereas L-leucine lacks this group. L-isoleucine's ring structure prevents it from assuming the op value to fit into an a helix, whereas L-isoleucine does not have a ring structure.arrow_forwardSamples of the octapeptide AVGWRVKS are subjected to proteolytic cleavage by either trypsin or chymotrypsin. Select the most appropriate technique for separating the digestion products of AVGWRVKS if cleaved by trypsin. salting out ion-exchange chromatography gel-filtration chromatography dialysis Select the most appropriate technique for separating the digestion products of AVGWRVKS if cleaved by chymotrypsin. ion-exchange chromatography gel-filtration chromatography dialysis salting outarrow_forward
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