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Organic Chemistry 9th edition [Kietas viršelis]

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(University of California, Los Angeles), (Beloit College), (University of Texas, Austin), (University of Texas, Austin)
  • Formatas: Hardback, 1408 pages, aukštis x plotis x storis: 50x228x281 mm, weight: 2789 g
  • Išleidimo metai: 05-Jun-2022
  • Leidėjas: Brooks/Cole
  • ISBN-10: 0357451864
  • ISBN-13: 9780357451861
Kitos knygos pagal šią temą:
  • Formatas: Hardback, 1408 pages, aukštis x plotis x storis: 50x228x281 mm, weight: 2789 g
  • Išleidimo metai: 05-Jun-2022
  • Leidėjas: Brooks/Cole
  • ISBN-10: 0357451864
  • ISBN-13: 9780357451861
Kitos knygos pagal šią temą:
ORGANIC CHEMISTRY, Ninth Edition, is revised to align with the way students approach complicated material. It includes pull-out organic chemistry reaction roadmaps organized by chapter to help you devise your own reaction pathways.

Emphasizing practical how-to skills, the new edition is packed with problems, along with hundreds of detailed solutions to all in-chapter exercises to guide you through logical approaches to solving problems.

New point-by-point summaries at the beginning of each section highlight important content in a way that is easy to review and reference, while in-margin definitions and highlighted integral concepts reinforce key content throughout the text. In the eBook and OWLv2 course, there are 100 author-created videos that explain and illustrate the most difficult concepts.
Preface xxix
Acknowledgments xxxv
1 Covalent Bonding and Shapes of Molecules
1(72)
1.1 Electronic Structure of Atoms
2(5)
1.2 Lewis Model of Bonding
7(13)
Careers In Chemistry Dahlia Haynes, Innovation Portfolio Manager and RDE Technical Leader, SC Johnson
12(4)
How To: Quickly Figure Out Formal Charge
16(2)
How To: Draw Lewis Structures from Condensed Structural Formulas
18(2)
1.3 Functional Groups
20(7)
1.4 Bond Angles and Shapes of Molecules
27(3)
1.5 Polar and Nonpolar Molecules
30(2)
MCAT Practice: Passage And Questions Fullerenes
30(2)
1.6 Quantum or Wave Mechanics
32(4)
1.7 A Combined Valence Bond and Molecular Orbital Theory Approach to Covalent Bonding
36(14)
Connections To Biological Chemistry Phosphoesters
44(5)
How To: Quickly Recognize the Hybridization and Geometry of Atoms
49(1)
1.8 Resonance
50(6)
How To: Draw Curved Arrows and Push Electrons in Creating Contributing Structures
51(5)
1.9 Molecular Orbitals for Delocalized Systems
56(6)
MCAT Practice: Passage And Questions Vsepr and Resonance
60(2)
1.10 Bond Lengths and Bond Strengths in Alkanes, Alkenes, and Alkynes
62(11)
Problems
63(10)
2 Alkanes and Cycloalkanes
73(57)
2.1 The Structure of Alkanes
74(2)
2.2 Constitutional Isomerism in Alkanes
76(2)
Careers In Chemistry Amy Rhoden Smith, Program Development Leader, Precision Biosciences
77(1)
2.3 Nomenclature of Alkanes and the IUPAC System
78(10)
2A Cycloalkanes
84(4)
2.5 Conformations of Alkanes and Cycloalkanes
88(14)
How To: Draw Alternative Chair Conformations of Cyclohexane
99(3)
2.6 Cisjrans Isomerism in Cycloalkanes and Bicycloalkanes
102(9)
How To: Convert Planar Cyclohexanes to Chair Cyclohexanes
104(6)
MCAT Practice: Passage And Questions Tetrodotoxin
110(1)
2.7 Physical Properties of Alkanes and Cycloalkanes
111(4)
2.8 Reactions of Alkanes
115(2)
2.9 Sources and Importance of Alkanes
117(13)
Chemical Connections Octane Rating: What Those Numbers at the Pump Mean
119(1)
Problems
120(10)
3 Stereoisomerism and Chirality
130(44)
3.1 Chirality--The Handedness of Molecules
131(1)
3.2 Stereoisomerism
132(6)
How To: Draw Chiral Molecules
134(3)
Careers In Chemistry Tricia Johnson, Chemist, U.S. Food and Drug Administration
137(1)
3.3 Naming Chiral Centers--The R,S System
138(4)
Careers In Chemistry Eric Breitung, Research Scientist, New York Metropolitan Museum of Art
140(1)
How To: Assign R or S Configuration to a Chiral Center
141(1)
3.4 Acyclic Molecules with Two or More Stereocenters
142(7)
How To: Quickly Draw and Recognize Enantiomers and Diastereomers
149(1)
3.5 Cyclic Molecules with Two or More Chiral Centers
149(4)
3.6 Tying All the Terminology Together
153(2)
3.7 Optical Activity--How Chirality Is Detected in the Laboratory
155(4)
3.8 The Significance of Chirality in the Biological World
159(4)
Connections To Biological Chemistry Chiral Drugs
161(1)
MCAT Practice: Passage And Questions Amino Acid Stereochemistry
161(2)
3.9 Separation of Enantiomers --Resolution
163(11)
Problems
166(8)
4 Acids and Bases
174(39)
4.1 Arrhenius Acids and Bases
175(1)
4.2 Bronsted-Lowry Acids and Bases
175(9)
Careers In Chemistry Baskar Nammalwar, Senior Scientist, Forge Therapeutics & Blacksmith Medicines
175(9)
4.3 Acid Dissociation Constants, pKa, and the Relative Strengths of Acids and Bases
184(2)
4.4 The Position of Equilibrium in Acid-Base Reactions
186(5)
How To: Calculate the Equilib hum Constants for Acid-Base Reactions
188(1)
Connections To Biological Chemistry The Ionization of Functional Groups at Physiological pH
189(2)
4.5 Thermochemistry and Mechanisms of Acid-Base Reactions
191(5)
4.6 Molecular Structure and Acidity
196(5)
MCAT Practice: Passage And Quesvons Acid-Base Equilibria
201(1)
4.7 Lewis Acids and Bases
201(12)
Problems
204(9)
5 Alkenes: Bonding, Nomenclature, and Properties
213(24)
5.1 Structure of Alkenes
215(3)
How To: Calculate the Index of Hydrogen Deficiency
215(3)
5.2 Nomenclature of Alkenes
218(8)
Careers In Chemistry Ingrid Monies, Professor of Organic Chemistry, University of Puerto Rico
219(7)
5.3 Physical Properties of Alkenes
226(1)
Chemical Connections The Case of the Iowa and New York Strains of the European Corn Borer
226(1)
5.4 Naturally Occurring Alkenes--Terpene Hydrocarbons
227(10)
Connections To Biological Chemistry The Importance of Cis Double Bonds in Fats Versus Oils
229(1)
Problems
230(7)
6 Reactions of Alkenes
237(61)
6.1 Reactions of Alkenes--An Overview
238(1)
6.2 Organic Reactions Involving Reactive Intermediates
239(3)
Careers In Chemistry Ryann Kress, Registered Nurse, Carilion Roanoke Memorial Hospital
242(1)
6.3 Terminology
242(3)
6.4 Electrophilic Additions
245(22)
6.5 Hydroboration-Oxidation
267(4)
6.6 Oxidation
271(6)
How To: Write a Balanced Half-Reaction
27(250)
6.7 Reduction
277(4)
Connections To Biological Chemistry Trans Fatly Acids: What They Are and How to Avoid Them
280(1)
6.8 Molecules Containing Chiral Centers as Reactants or Products
281(17)
Problems
286(12)
7 Alkynes
298(40)
7.1 Structure of Alkynes
299(1)
7.2 Nomenclature of Alkynes
300(2)
7.3 Physical Properties of Alkynes
302(1)
7.4 Acidity of 1-Alkynes
302(1)
Careers In Chemistry Ivy Tran, Technical Sales Representative, Arclin USA
302(1)
7.5 Preparation of Alkynes
303(4)
7.6 Reaction Mechanisms
307(7)
7.7 Electrophilic Addition to Alkynes
314(3)
7.8 Hydration of Alkynes to Aldehydes and Ketones
317(6)
7.9 Reduction of Alkynes
323(3)
7.10 Organic Synthesis
326(12)
Problems
330(8)
8 Haloalkanes, Halogenation, and Radical Reactions
338(40)
8.1 Structure
339(1)
8.2 Nomenclature
339(2)
8.3 Physical Properties of Haloalkanes
341(4)
8.4 Preparation of Haloalkanes by Halogenation of Alkanes
345(5)
Careers In Chemistry Jonathan C. Trent, Associate Director for Clinical Research and the Director of the Bone and Soft-Tissue Sarcoma Group, Sylvester Comprehensive Cancer Center
345(5)
8.5 Mechanism of Halogenation of Alkanes
350(8)
Chemical Connections Freons
353(5)
8.6 Allylic Halogenation
358(5)
8.7 Radical Autoxidation
363(4)
MCAT Practice: Passage And Questions Antioxidants
365(2)
8.8 Radical Addition of HBr to Alkenes
367(11)
Problems
371(7)
9 Nucleophilic Substitution and β-Elimination
378(65)
9.1 Nucleophilic Substitution in Haloalkanes
379(2)
Careers In Chemistry Halimatu S. Mohammed, Technical Transfer Specialist, WuXi Advanced Therapies
380(1)
9.2 Mechanisms of Nucleophilic Aliphatic Substitution
381(5)
9.3 Experimental Evidence for SN1 and SN2 Mechanisms
386(17)
9.4 Analysis of Several Nucleophilic Substitution Reactions
403(3)
9.5 β-Elimination
406(3)
9.6 Mechanisms of β-Elimination
409(3)
9.7 Experimental Evidence for El and E2 Mechanisms
412(7)
9.8 Substitution Versus Elimination
419(5)
9.9 Analysis of Several Competitions Between Substitutions and Eliminations
424(3)
MCAT Practice: Passage And Quesvons Solvents and Solvation
426(1)
9.10 Neighboring Group Participation
427(16)
Connections To Biological Chemistry Mustard Gases and the Treatment of Neoplastic Diseases
430(2)
Problems
432(11)
10 Alcohols
443(55)
10.1 Structure and Nomenclature of Alcohols
444(3)
Careers In Chemistry Dana L. Broughton, Patent Attorney, GlaxoSmithKline
445(2)
10.2 Physical Properties of Alcohols
447(4)
Connections To Biological Chemistry The Importance of Hydrogen Bonding in Drug-Receptor Interactions
449(2)
10.3 Acidity and Basicity of Alcohols
451(2)
10.4 Reaction of Alcohols with Active Metals
453(1)
10.5 Conversion of Alcohols to Haloalkanes and Sulfonates
454(8)
10.6 Acid-Catalyzed Dehydration of Alcohols
462(6)
10.7 The Pinacol Rearrangement
468(4)
MCAT Practice: Passage And Questions Pinacol Rearrangement
471(1)
10.8 Oxidation of Alcohols
472(11)
Chemical Connections Blood Alcohol Screening
476(4)
Connections To Biological Chemistry The Oxidation of Alcohols by NAD+
480(2)
MCAT Practice: Passage And Questions Alcohol Oxidations
482(1)
10.9 Thiols
483(15)
Problems
488(10)
11 Ethers, Epoxides, and Sulfides
498(46)
11.1 Structure of Ethers
499(1)
11.2 Nomenclature of Ethers
499(2)
11.3 Physical Properties of Ethers
501(2)
Careers In Chemistry Miriam Quintal, Managing Principal, Lewis-Burke Associates LLC
502(1)
11.4 Preparation of Ethers
503(5)
11.5 Reactions of Ethers
508(3)
11.6 Silyl Ethers as Protecting Groups
511(3)
11.7 Epoxides: Structure and Nomenclature
514(1)
11.8 Synthesis of Epoxides
515(6)
11.9 Reactions of Epoxides
521(6)
MCAT Practice: Passage And Questions Benzo[ a]pyrene
525(2)
11.10 Ethylene Oxide and Epichlorohydrin: Building Blocks in Organic Synthesis
527(2)
11.11 Crown Ethers
529(1)
11.12 Sulfides
530(14)
Problems
533(11)
12 Infrared Spectroscopy
544(23)
12.1 Electromagnetic Radiation
545(1)
12.2 Molecular Spectroscopy
546(1)
12.3 Infrared Spectroscopy
547(7)
Careers In Chemistry LaShondo T. Cureton, Lead Chemist, U.S. Food and Drug Administration
547(7)
12.4 Interpreting Infrared Spectra
554(9)
12.5 Solving Infrared Spectral Problems
563(4)
Problems
564(3)
13 Nuclear Magnetic Resonance Spectroscopy
567(48)
13.1 Nuclear Spin States
568(1)
Careers In Chemistry Sathish Kumar Lageshetty, Senior Scientist, CHASM Advanced Materials, Inc.
568(1)
13.2 Orientation of Nuclear Spins in an Applied Magnetic Field
569(2)
13.3 Nuclear Magnetic "Resonance"
571(2)
13.4 An NMR Spectrometer
573(2)
13.5 Equivalent Hydrogens
575(3)
13.6 Signal Areas
578(1)
13.7 Chemical Shift
579(5)
13.8 Signal Splitting and the (n + 1) Rule
584(2)
13.9 The Origins of Signal Splitting
586(8)
13.10 Stereochemistry and Topicity
594(4)
Chemical Connections Magnetic Resonance Imaging
597(1)
13.11 13C-NMR
598(2)
13.12 Interpretation of NMR Spectra
600(15)
How To: Solve NMR Spectral Problems
603(3)
Problems
606(9)
14 Mass Spectrometry
615(24)
14.1 A Mass Spectrometer
616(3)
14.2 Features of a Mass Spectrum
619(4)
Careers In Chemistry RaiAnna Arscott Hopson, Scientist, AMVAC Chemical Corp
620(3)
14.3 Interpreting Mass Spectra
623(10)
Connections To Biological Chemistry Mass Spectrometry of Biological Macromolecules
631(2)
14.4 Mass Spectrometry in the Organic Synthesis Laboratory and Other Applications
633(6)
Problems
634(5)
15 An Introduction to Organometallic Compounds
639(24)
15.1 Organomagnesium and Organolithium Compounds
640(6)
Careers In Chemistry Kevin Meraz, Senior Scientist, FDD Inc.
643(3)
15.2 Lithium Diorganocopper (Gilman) Reagents
646(4)
15.3 Carbenes and Carbenoids
650(13)
MCAT Practice: Passage And Questions Inorganic Coordination Compounds
655(1)
Problems
656(7)
16 Aldehydes and Ketones
663(76)
16.1 Structure and Bonding
664(1)
Careers In Chemistry Weijun Niu, Research Associate, Corning
664(1)
16.2 Nomenclature
664(5)
16.3 Physical Properties
669(1)
16.4 Reactions
670(2)
16.5 Addition of Carbon Nucleophiles
672(7)
16.6 The Wittig Reaction
679(5)
16.7 Addition of Oxygen Nucleophiles
684(10)
16.8 Addition of Nitrogen Nucleophiles
694(6)
MCAT Practice: Passage And Questions Pyridoxine (Vitamin BJ: A Carrier of Amino Groups
698(2)
16.9 Keto-Enol Tautomerism
700(5)
16.10 Oxidation
705(3)
16.11 Reduction
708(10)
Connections To Biological Chemistry Nadh: The Biological Equivalent of a Hydride Reducing Agent
713(1)
How To: Retrosynthetically Dissect an Amine into the Proper Starting Materials for a Reductive Amination
714(4)
16.12 Reactions at an a-Carbon
718(21)
Problems
721(18)
17 Carboxylic Acids
739(38)
17.1 Structure
740(1)
17.2 Nomenclature
740(4)
Careers In Chemistry James Mack, Professor of Chemistry, University of Cincinnati
741(3)
17.3 Physical Properties
744(3)
Chemical Connections From Willow Bark to Aspirin and Beyond
745(2)
17.4 Acidity
747(5)
17.5 Preparation of Carboxylic Acids
752(1)
17.6 Reduction
752(3)
Chemical Connections Industrial Synthesis of Acetic Acid-Transition Metal Catalysis
753(2)
17.7 Esterification
755(3)
Chemical Connections Esters as Flavoring Agents
757(1)
17.8 Conversion to Acid Chlorides
758(3)
MCAT Practice: Passage And Quesvons Permethrin and Bifenthrin
760(1)
17.9 Decarboxylation
761(16)
Connections To Biological Chemistry Ketone Bodies and Diabetes Mellitus
763(2)
Problems
765(12)
18 Functional Derivatives of Carboxylic Acids
777(69)
18.1 Structure and Nomenclature
778(6)
Chemical Connections From Cocaine to Procaine and Beyond
781(1)
Chemical Connections From Moldy Clover to a Blood Thinner
782(2)
18.2 Acidity of Amides, Imides, and Sulfonamides
784(3)
Connections To Biological Chemistry The Unique Structure of Amide Bonds
786(1)
18.3 Characteristic Reactions
787(4)
18.4 Carboxylic Acid Derivative Reaction Mechanisms
791(4)
Careers In Chemistry Shelbie Shelder, Family Medicine Doctor and Resident Physician, Seattle Indian Health Board and Swedish First Hill Hospital
791(4)
18.5 Reaction with Water: Hydrolysis
795(14)
Chemical Connections Mechanistic Alternatives for Ester Hydrolysis: SN2 and SNI Possibilities
803(6)
18.6 Reaction with Alcohols
809(4)
18.7 Reactions with Ammonia and Amines
813(3)
18.8 Reaction of Acid Chlorides with Salts of Carboxylic Acids
816(1)
18.9 Interconversion of Functional Derivatives
816(3)
MCAT Practice: Passage And Questions B-Lactam Antibiotics
817(2)
18.10 Reactions with Organometallic Compounds
819(4)
18.11 Reduction
823(23)
Problems
829(17)
19 Enolate Anions and Enamines
846(75)
19.1 Formation and Reactions of Enolate Anions: An Overview
847(2)
19.2 Aldol Reaction
849(9)
Careers In Chemistry Rami Abu-Aita, Chief Medical Physicist, SSM Health for the South Central Wisconsin region
849(9)
19.3 Claisen and Dieckmann Condensations
858(7)
19.4 Claisen and Aldol Condensations in the Biological World
865(3)
Chemical Connections Drugs That Lower Plasma Levels of Cholesterol
866(2)
19.5 Enamines
868(5)
19.6 Acetoacetic Ester Synthesis
873(5)
19.7 Malonic Ester Synthesis
878(4)
19.8 Conjugate Addition to α,β-Unsaturated Carbonyl Compounds
882(10)
19.9 Crossed Enolate Reactions Using LDA
892(29)
MCAT Practice: Passage And Questions Ibuprofen: The Evolution of an Industrial Synthesis
897(2)
Problems
899(22)
20 Dienes, Conjugated Systems, and Pericyclic Reactions
921(47)
20.1 Stability of Conjugated Dienes
922(4)
Careers In Chemistry Paul Cunningham, Small Animal Emergency Veterinarian Animal Emergency Centre Pty Ltd.
923(3)
20.2 Electrophilic Addition to Conjugated Dienes
926(7)
20.3 UV-Visible Spectroscopy
933(6)
Chemical Connections Curry and Cancer
939(1)
20.4 Pericyclic Reaction Theory
939(3)
20.5 The Diels-Alder Reaction
942(10)
20.6 Sigmatropic Shifts
952(16)
Problems
958(10)
21 Benzene and the Concept of Aromaticity
968(59)
21.1 The Structure of Benzene
969(5)
Careers In Chemistry Chinenyeze Nwankwoala, Senior Chemist, Ascend Performance Materials
969(5)
21.2 The Concept of Aromaticity
974(12)
How To: Recognize Aromatic Compounds: Criteria and Caveats
986(1)
21.3 Nomenclature
986(4)
21.4 Phenols
990(11)
MCAT Practice: Passage And Questions Capsaicin, "Some Like It Hot"
996(5)
21.5 Reactions at a Benzylic Position
1001(26)
Problems
1006(21)
22 Reactions of Benzene and Its Derivatives
1027(45)
22.1 Electrophilic Aromatic Substitution
1028(13)
Careers In Chemistry Goupu Touthang, Research Chemist, MECS Sulfuric Acid and Environmental Technologies
1028(13)
22.2 Disubstitution and Polysubstitution
1041(9)
22.3 Nucleophilic Aromatic Substitution
1050(22)
Problems
1055(17)
23 Amines
1072(59)
23.1 Structure and Classification
1073(1)
23.2 Nomenclature
1074(4)
Careers In Chemistry Brent Dial, Research Scientist: Organic Chemist, Oak Ridge National Laboratory
1075(3)
23.3 Chirality of Amines and Quaternary Ammonium Ions
1078(1)
23.4 Physical Properties
1079(2)
Chemical Connections The Poison Dart Frogs of South America
1080(1)
23.5 Basicity
1081(9)
MCAT Practice: Passage And Questions The Planarily of--NH2 Groups on Heterocyclic Rings
1086(4)
23.6 Reactions with Acids
1090(4)
23.7 Preparation
1094(3)
23.8 Reaction with Nitrous Acid
1097(11)
23.9 Hofmann Elimination
1108(3)
23.10 Cope Elimination
1111(20)
Problems
1113(18)
24 Catalytic Carbon-Carbon Bond Formation
1131(43)
24.1 Carbon-Carbon Bond-Forming Reactions from Earlier
Chapters
1132(1)
Careers In Chemistry Arnie R. de Leon, Senior Process Development Group Leader, Nilto Denko Avecia Inc.
1132(1)
24.2 Organometallic Compounds and Catalysis
1133(1)
24.3 The Heck Reaction
1134(7)
24.4 Catalytic Allylic Alkylation
1141(4)
24.5 Palladium-Catalyzed Cross-Coupling Reactions
1145(7)
24.6 Alkene Metathesis
1152(3)
24.7 Click Chemistry
1155(19)
Problems
1157(17)
25 Carbohydrates
1174(37)
25.1 Monosaccharides
1175(6)
Careers In Chemistry Luis Ernesto Miramontes Cardenas, Chemist
1180(1)
25.2 The Cyclic Structure of Monosaccharides
1181(12)
Chemical Connections L-Ascorbic Acid (Vitamin C)
1184(9)
25.3 Reactions of Monosaccharides
1186(7)
Chemical Connections Testing for Glucose
1193(1)
MCAT Practice: Passage And Questions Fucose
1194(1)
25.4 Disaccharides and Oligosaccharides
1195(4)
Chemical Connections A, B, AB, and O Blood Group Substances
1198(1)
25.5 Polysaccharides
1199(3)
Chemical Connections High-Fructose Corn Syrup
1201(1)
25.6 Glucosaminoglycans
1202(9)
Problems
1203(8)
26 Organic Polymer Chemistry
1211(1)
26.1 The Architecture of Polymers
1212(1)
26.2 Polymer Notation and Nomenclature
1213(2)
Careers In Chemistry Percy Lavon Julian, Director, Julian Laboratories
1214(1)
26.3 Molecular Weights of Polymers
1215(1)
26.4 Polymer Morphology--Crystalline Versus Amorphous Materials
1215(2)
26.5 Step-Growth Polymerizations
1217(8)
Chemical Connections Stitches That Dissolve
1224(1)
26.6 Chain-Growth Polymerizations
1225(4)
Chemical Connections Organic Polymers That Conduct Electricity
1229(8)
MCAT Practice: Passage And Questions The Chemistry of Superglue
1237(5)
Chemical Connections Recycling of Plastics
1242(2)
Problems
1244
27 Lipids
1(30)
27.1 Triglycerides
2(3)
27.2 Soaps and Detergents
5(4)
Connections To Biological Chemistry FAD/FADH2: Agents for Electron Transfer in Biological Oxidation-Reductions: Fatty Acid Oxidation
7(2)
27.3 Prostaglandins
9(2)
27.4 Steroids
11(5)
27.5 Phospholipids
16(2)
Chemical Connections Snake Venom Phospholipases
17(1)
27.6 Fat-Soluble Vitamins
18(13)
Mcat Practice: Passage And Questions Vitamin K, Blood Clotting, and Basicity
21(4)
Problems
25(6)
28 Amino Acids and Proteins
31(40)
28.1 Amino Acids
31(4)
28.2 Acid-Base Properties of Amino Acids
35(5)
28.3 Polypeptides and Proteins
40(1)
28.4 Primary Structure of Polypeptides and Proteins
41(7)
28.5 Synthesis of Polypeptides
48(5)
28.6 Three-Dimensional Shapes of Polypeptides and Proteins
53(18)
Chemical Connections Spider Silk
57(7)
Problems
64(7)
29 Nucleic Acids
71(1)
29.1 Nucleosides and Nucleotides
72(2)
29.2 The Structure of DNA
74(7)
Chemical Connections The Search for Antiviral Drugs
77(4)
29.3 Ribonucleic Acids
81(3)
Chemical Connections The Fountain of Youth
82(2)
29.4 The Genetic Code
84(2)
29.5 Sequencing Nucleic Acids
86(4)
Chemical Connections DNA Fingerprinting
90(4)
Problems
94
Appendices
1 Thermodynamics and the Equilibrium Constant
1(1)
2 Major Classes of Organic Acids
2(1)
3 Bond Dissociation Enthalpies
3(1)
4 Characteristic 1H-NMR Chemical Shifts
4(1)
5 Characteristic 13C-NMR Chemical Shifts
5(1)
6 Characteristic Infrared Absorption Frequencies
6(1)
7 Electrostatic Potential Maps
7(1)
8 Summary of Stereochemical Terms
8(3)
9 Summary of the Rules of Nomenclature
11
10 Organic Chemistry Reaction Roadmaps Insert
Glossary 1(1)
Index 1
William H. Brown is emeritus professor of chemistry at Beloit College, where he was twice named Teacher of the Year. His teaching responsibilities include organic chemistry, advanced organic chemistry and, more recently, special topics in pharmacology and drug synthesis. He received his Ph.D. from Columbia University under the direction of Gilbert Stork and did postdoctoral work at California Institute of Technology and the University of Arizona. Brent L. Iverson is the Warren J. and Viola Mae Raymer Professor, a University Distinguished Teaching Professor and the dean of the School of Undergraduate Studies at The University of Texas at Austin. His research spans the interface of organic chemistry and molecular biology. His group has developed several patented technologies, including an FDA-approved treatment for late-stage anthrax. Eric Anslyn received his Ph.D. from California Institute of Technology. He is the Welch Regents Chair of Chemistry and a University Distinguished Teaching Professor at The University of Texas at Austin, as well as an HHMI Professor. His research focuses on the physical and bioorganic chemistry of synthetic and natural receptors and catalysts. Christopher S. Foote was a professor of chemistry at the University of California, Los Angeles. His scholarly credits included Sloan Fellow; Guggenheim Fellow; ACS Baekland Award; ACS Cope Scholar; Southern California Section ACS Tolman Medal; President, American Society for Photobiology; and Senior Editor, Accounts of Chemical Research.