EBK ORGANIC CHEMISTRY
7th Edition
ISBN: 9780133556186
Author: Bruice
Publisher: VST
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Textbook Question
Chapter 22.7, Problem 24P
Esterase is an enzyme that catalyzes the hydrolysis of esters. It hydrolyzes esters of L-amino acids more rapidly than esters of D-amino acids. How can this enzyme be used to separate a racemic mixture of amino acids?
Expert Solution & Answer
Trending nowThis is a popular solution!
Students have asked these similar questions
When two solutions, one of 0.1 M KCl (I) and the other of 0.1 M MCl (II), are brought into contact by a membrane. The cation M cannot cross the membrane. At equilibrium, x moles of K+ will have passed from solution (I) to (II). To maintain the neutrality of the two solutions, x moles of Cl- will also have to pass from I to II. Explain this equality: (0.1 - x)/x = (0.1 + x)/(0.1 - x)
Calculate the variation in the potential of the Pt/MnO4-, Mn2+ pair with pH, indicating the value of the standard potential. Data: E0 = 1.12.
Given the cell: Pt l H2(g) l dis X:KCl (sat) l Hg2Cl2(s) l Hg l Pt. Calculate the emf of the cell as a function of pH.
Chapter 22 Solutions
EBK ORGANIC CHEMISTRY
Ch. 22.1 - a. Explain why, when the imidazole ring of...Ch. 22.2 - a. Which isomer(R)-alanine or (S)-alanineis...Ch. 22.2 - Prob. 4PCh. 22.3 - Prob. 5PCh. 22.3 - Prob. 6PCh. 22.3 - Draw the predominant form for glutamate in a...Ch. 22.3 - a. Why is the pKa of the glutamate side chain...Ch. 22.4 - Explain why the pI of lysine is the average of the...Ch. 22.4 - Calculate the pI of each of the following amino...Ch. 22.4 - a. Which amino acid has the lowest pI value? b....
Ch. 22.4 - Prob. 13PCh. 22.5 - What aldehyde is formed when valine is treated...Ch. 22.5 - Prob. 15PCh. 22.5 - Prob. 16PCh. 22.5 - Prob. 17PCh. 22.5 - Prob. 18PCh. 22.6 - Why is excess ammonia used in the preceding...Ch. 22.6 - Prob. 20PCh. 22.6 - What amino acid is formed using the...Ch. 22.6 - Prob. 22PCh. 22.6 - What amino acid is formed when the aldehyde used...Ch. 22.7 - Esterase is an enzyme that catalyzes the...Ch. 22.8 - Draw the tetrapeptide Ala-Thr-Asp-Asn and indicate...Ch. 22.8 - Prob. 26PCh. 22.8 - Prob. 27PCh. 22.8 - Which bonds in the backbone of a peptide can...Ch. 22.9 - What is the configuration about each of the...Ch. 22.9 - Glutathione is a tripeptide whose function is to...Ch. 22.10 - What dipeptides would be formed by heating a...Ch. 22.10 - Suppose you are trying to synthesize the dipeptide...Ch. 22.10 - Show the steps in the synthesis of the...Ch. 22.10 - a. Calculate the overall yield of bradykinin when...Ch. 22.11 - Show the steps in the synthesis of the...Ch. 22.13 - Prob. 36PCh. 22.13 - In determining the primary structure of insulin,...Ch. 22.13 - A decapeptide undergoes partial hydrolysis to give...Ch. 22.13 - Explain why cyanogen bromide does not cleave on...Ch. 22.13 - Indicate the peptides produced from cleavage by...Ch. 22.13 - Prob. 42PCh. 22.13 - Three peptides were obtained from a trypsin...Ch. 22.14 - Prob. 44PCh. 22.15 - How would a protein that resides in the nonpolar...Ch. 22.16 - a. Which would have the greatest percentage of...Ch. 22 - Prob. 47PCh. 22 - Glycine has pK2 values of 2.34 and 9.60. At what...Ch. 22 - Prob. 49PCh. 22 - Prob. 50PCh. 22 - Aspartame (its structure is on page 1007) has a pl...Ch. 22 - Draw the form of aspartate that predominates at...Ch. 22 - A professor was preparing a manuscript for...Ch. 22 - Prob. 54PCh. 22 - Determine the amino acid sequence of a polypeptide...Ch. 22 - Prob. 56PCh. 22 - Which is the more effective buffer at...Ch. 22 - Identify the location and type of charge on the...Ch. 22 - Draw the product obtained when a lysine side chain...Ch. 22 - After the polypeptide shown below was treated with...Ch. 22 - Treatment of a polypeptide with 2-mercaptoethanol...Ch. 22 - Show how aspartame can be synthesized using DCCD.Ch. 22 - -Amino acids can be prepared by treating an...Ch. 22 - Reaction of a polypeptide with carboxypeptidase A...Ch. 22 - a. How many different octapeptides can be made...Ch. 22 - Glycine has pKa values of 2.3 and 9.6. Do you...Ch. 22 - A mixture of 15 amino acids gave the fingerprint...Ch. 22 - Write the mechanism for the reaction of an amino...Ch. 22 - Prob. 69PCh. 22 - Show how valine can be prepared by a. a...Ch. 22 - A chemist wanted to test his hypothesis that the...Ch. 22 - Propose a mechanism for the rearrangement of the...Ch. 22 - A normal polypeptide and a mutant of the...Ch. 22 - Determine the amino acid sequence of a polypeptide...
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- The decimolar calomel electrode has a potential of 0.3335 V at 25°C compared to the standard hydrogen electrode. If the standard reduction potential of Hg22+ is 0.7973 V and the solubility product of Hg2Cl2 is 1.2x 10-18, find the activity of the chlorine ion at this electrode.Data: R = 8.314 J K-1 mol-1, F = 96485 C mol-1, T = 298.15 K.arrow_forward2. Add the following group of numbers using the correct number of significant figures for the answer. Show work to earn full credit such as rounding off the answer to the correct number of significant figures. Replace the question marks with the calculated answers or write the calculated answers near the question marks. 10916.345 37.40832 5.4043 3.94 + 0.0426 ? (7 significant figures)arrow_forwardThe emf at 25°C of the cell: Pt l H2(g) l dis X:KCl (sat) l Hg2Cl2(s) l Hg l Pt was 612 mV. When solution X was replaced by normal phosphate buffer solution with a pH of 6.86, the emf was 741 mV. Calculate the pH of solution X.arrow_forward
- Indicate how to calculate the potential E of the reaction Hg2Cl2(s) + 2e ⇄ 2Hg + 2Cl- as a function of the concentration of Cl- ions. Data: the solubility product of Hg2Cl2.arrow_forwardHow can Beer’s Law be used to determine the concentration in a selected food sample. Provide an in-depth discussion and examples of this.arrow_forwardb) H3C- H3C Me CH 3 I HN Me H+arrow_forward
- Using Luther's rule, determine the reference potentials of the electrodes corresponding to the low stability systems Co³+/Co and Cr²+/Cr from the data in the table. Electrodo ΕΝ Co²+/Co Co3+/Co²+ -0,28 +1,808 Cr³+ / Cr -0,508 Cr3+ / Cr²+ -0,41arrow_forwardThe molecule PYRIDINE, 6tt electrons and is there pore aromuntre and is Assigned the Following structure contenus Since aromatk moleculey undergo electrophilic allomatic substitution, Pyridine should undergo The Following reaction + HNO3 12504 a. write all of the possible Mononitration Products that could Result From this roaction Based upon the reaction the reaction mechanism determine which of these producty would be the major Product of the hegetionarrow_forwardUsing Benzene as starting materia Show how each of the Following molecules could Ve synthesked 9. CHI d. 10450 b 0 -50311 ८ City -5034 1-0-650 e NO2arrow_forward
- BA HBr of the fol 1)=MgCI 2) H₂O major NaOEt Ts Cl Py (pyridine) 1) 03 2) Me2S 1arrow_forward4. Provide a clear arrow-pushing mechanism for the following reactions. Do not skip proton transfers, do not combine steps, and make sure your arrows are clear enough to be interpreted without ambiguity. a) NHBoc ⚫OBn HO. H3C CO2CH3 -OBn H3C H3C. H3C. NHBOC CI CO2CH3arrow_forwardDraw structures of the following compounds and identify their role: mCPBA (MCPBA) DMS Py 9-BBN LAH Sia₂BH TsCI PCC t-BuOK LDA MeLi n-BuLi DMSO DMF Sodium Borohydride Lithium DiisopropylAmide 2arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning
World of ChemistryChemistryISBN:9780618562763Author:Steven S. ZumdahlPublisher:Houghton Mifflin College Div
Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning
Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning
General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning
Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,
World of Chemistry, 3rd edition
Chemistry
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Brooks / Cole / Cengage Learning
World of Chemistry
Chemistry
ISBN:9780618562763
Author:Steven S. Zumdahl
Publisher:Houghton Mifflin College Div
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Introduction to General, Organic and Biochemistry
Chemistry
ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Cengage Learning
General, Organic, and Biological Chemistry
Chemistry
ISBN:9781285853918
Author:H. Stephen Stoker
Publisher:Cengage Learning
Organic And Biological Chemistry
Chemistry
ISBN:9781305081079
Author:STOKER, H. Stephen (howard Stephen)
Publisher:Cengage Learning,
Biomolecules - Protein - Amino acids; Author: Tutorials Point (India) Ltd.;https://www.youtube.com/watch?v=ySNVPDHJ0ek;License: Standard YouTube License, CC-BY