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Organic chemistry with biological applications Cover Image Book Book

Organic chemistry with biological applications

McMurry, John (author.).

Summary: "Renowned for its student-friendly writing style and fresh perspective, John McMurry's ORGANIC CHEMISTRY WITH BIOLOGICAL APPLICATIONS provides full coverage of the foundations of organic chemistry -- enhanced by biological examples throughout. In addition, McMurry discusses the organic chemistry behind biological pathways. The third edition is updated with new problems, illustrations, and essays. Available digital options include the MindTap® Reader and OWLv2, the leading online homework and learning system for chemistry."--Publisher's website.

Record details

  • ISBN: 9781285842912
  • ISBN: 128584291X
  • ISBN: 128586784X
  • ISBN: 9781285867847
  • Physical Description: print
    1 volume (various pagings) : color illustrations ; 25 cm
  • Edition: 3rd Edition.
  • Publisher: Stamford, CT : Cengage Learning, [2015]

Content descriptions

General Note:
Includes index.
Formatted Contents Note: Machine generated contents note: 1. Structure and Bonding -- 1-1. Atomic Structure: The Nucleus -- 1-2. Atomic Structure: Orbitals -- 1-3. Atomic Structure: Electron Configurations -- 1-4. Development of Chemical Bonding Theory -- 1-5. Describing Chemical Bonds: Valence Bond Theory -- 1-6. SP3 Hybrid Orbitals and the Structure of Methane -- 1-7. SP3 Hybrid Orbitals and the Structure of Ethane -- 1-8. SP2 Hybrid Orbitals and the Structure of Ethylene -- 1-9. SP Hybrid Orbitals and the Structure of Acetylene -- 1-10. Hybridization of Nitrogen, Oxygen, Phosphorus, and Sulfur -- 1-11. Describing Chemical Bonds: Molecular Orbital Theory -- 1-12. Drawing Chemical Structures -- Something Extra Organic Foods: Risk versus Benefit -- 2. Polar Covalent Bonds; Acids and Bases -- 2-1. Polar Covalent Bonds: Electronegativity -- 2-2. Polar Covalent Bonds: Dipole Moments -- 2-3. Formal Charges -- 2-4. Resonance -- 2-5. Rules for Resonance Forms -- 2-6. Drawing Resonance Forms -- 2-7. Acids and Bases: The Brønsted-Lowry Definition -- 2-8. Acid and Base Strength -- 2-9. Predicting Acid-Base Reactions from pKa Values -- 2-10. Organic Acids and Organic Bases -- 2-11. Acids and Bases: The Lewis Definition -- 2-12. Noncovalent Interactions between Molecules -- Something Extra Alkaloids: From Cocaine to Dental Anesthetics -- 3. Organic Compounds: Alkanes and Their Stereochemistry -- 3-1. Functional Croups -- 3-2. Alkanes and Alkane Isomers -- 3-3. Alkyl Groups -- 3-4. Naming Alkanes -- 3-5. Properties of Alkanes -- 3-6. Conformations of Ethane -- 3-7. Conformations of Other Alkanes -- Something Extra Gasoline -- 4. Organic Compounds: Cycloalkanes and Their Stereochemistry -- 4-1. Naming Cycloalkanes -- 4-2. Cis-Trans Isomerism in Cycloalkanes -- 4-3. Stability of Cycloalkanes: Ring Strain -- 4-4. Conformations of Cycloalkanes -- 4-5. Conformations of Cyclohexane -- 4-6. Axial and Equatorial Bonds in Cyclohexane -- 4-7. Conformations of Monosubstituted Cyclohexanes -- 4-8. Conformations of Disubstituted Cyclohexanes -- 4-9. Conformations of Polycyclic Molecules -- Something Extra Molecular Mechanics -- 5. Stereochemistry at Tetrahedral Centers -- 5-1. Enantiomers and the Tetrahedral Carbon -- 5-2. Reason for Handedness in Molecules: Chirality -- 5-3. Optical Activity -- 5-4. Pasteur's Discovery of Enantiomers -- 5-5. Sequence Rules for Specifying Configuration -- 5-6. Diastereomers -- 5-7. Meso Compounds -- 5-8. Racemic Mixtures and the Resolution of Enantiomers -- 5-9. Review of Isomerism -- 5-10. Chirality at Nitrogen, Phosphorus, and Sulfur -- 5-11. Prochirality -- 5-12. Chirality in Nature and Chiral Environments -- Something Extra Chiral Drugs -- 6. Overview of Organic Reactions -- 6-1. Kinds of Organic Reactions -- 6-2. How Organic Reactions Occur: Mechanisms -- 6-3. Radical Reactions -- 6-4. Polar Reactions -- 6-5. Example of a Polar Reaction: Addition of H2O to Ethylene -- 6-6. Using Curved Arrows in Polar Reaction Mechanisms -- 6-7. Describing a Reaction: Equilibria, Rates, and Energy Changes -- 6-8. Describing a Reaction: Bond Dissociation Energies -- 6-9. Describing a Reaction: Energy Diagrams and Transition States -- 6-10. Describing a Reaction: Intermediates -- 6-11. Comparison between Biological Reactions and Laboratory Reactions -- Something Extra Where Do Drugs Come From? -- 7. Alkenes and Alkynes -- 7-1. Calculating the Degree of Unsaturation -- 7-2. Naming Alkenes and Alkynes -- 7-3. Cis-Trans Isomerism in Alkenes -- 7-4. Alkene Stereochemistry and the E,Z Designation -- 7-5. Stability of Alkenes -- 7-6. Electrophilic Addition Reactions of Alkenes -- Writing Organic Reactions -- 7-7. Orientation of Electrophilic Addition: Markovnikov's Rule -- 7-8. Carbocation Structure and Stability -- 7-9. Hammond Postulate -- 7-10. Evidence for the Mechanism of Electrophilic Additions: Carbocation Rearrangements -- Something Extra Terpenes: Naturally Occurring Alkenes -- 8. Reactions of Alkenes and Alkynes j -- 8-1. Preparing Alkenes: A Preview of Elimination Reactions -- 8-2. Halogenation of Alkenes -- 8-3. Halohydrins from Alkenes -- 8-4. Hydration of Alkenes -- 8-5. Reduction of Alkenes: Hydrogenation -- 8-6. Oxidation of Alkenes: Epoxidation -- 8-7. Oxidation of Alkenes: Hydroxylation -- 8-8. Oxidation of Alkenes: Cleavage to Carbonyl Compounds -- 8-9. Addition of Carbenes to Alkenes: Cyclopropane Synthesis -- 8-10. Radical Additions to Alkenes: Chain-Growth Polymers -- 8-11. Biological Additions of Radicals to Alkenes -- 8-12. Conjugated Dienes -- 8-13. Reactions of Conjugated Dienes -- 8-14. Diels-Alder Cycloaddition Reaction -- 8-15. Reactions of Alkynes -- Something Extra--Natural Rubber -- Learning Reactions -- 9. Aromatic Compounds -- 9-1. Naming Aromatic Compounds -- 9-2. Structure and Stability of Benzene -- 9-3. Aromaticity and the Huckel 4n + 2 Rule -- 9-4. Aromatic Ions and Aromatic Heterocycles -- 9-5. Polycyclic Aromatic Compounds -- 9-6. Reactions of Aromatic Compounds: Electrophilic Substitution -- 9-7. Alkylation and Acylation of Aromatic Rings: The Friedel--Crafts Reaction -- 9-8. Substituent Effects in Electrophilic Substitutions -- 9-9. Nucleophilic Aromatic Substitution -- 9-10. Oxidation and Reduction of Aromatic Compounds -- 9-11. Introduction to Organic Synthesis: Polysubstituted Benzenes -- Something Extra Aspirin, NSAIDs, and COX-2 Inhibitors -- 10. Structure Determination: Mass Spectrometry, Infrared Spectroscopy, and Ultraviolet Spectroscopy -- 10-1. Mass Spectrometry of Small Molecules: Magnetic-Sector Instruments -- 10-2. Interpreting Mass Spectra -- 10-3. Mass Spectrometry of Some Common Functional Groups -- 10-4. Mass Spectrometry in Biological Chemistry: Time-of-Flight (TOF) Instruments -- 10-5. Spectroscopy and the Electromagnetic Spectrum -- 10-6. Infrared Spectroscopy -- 10-7. Interpreting Infrared Spectra -- 10-8. Infrared Spectra of Some Common Functional Groups -- 10-9. Ultraviolet Spectroscopy -- 10-10. Interpreting Ultraviolet Spectra: The Effect of Conjugation -- 10-11. Conjugation, Color, and the Chemistry of Vision -- Something Extra X-Ray Crystallography -- Structure Determination: Nuclear Magnetic Resonance Spectroscopy -- 11-1. Nuclear Magnetic Resonance Spectroscopy -- 11-2. Nature of NMR Absorptions -- 11-3. Chemical Shifts -- 11-4. 13C NMR Spectroscopy: Signal Averaging and FT-NMR -- 11-5. Characteristics of 13C NMR Spectroscopy -- 11-6. DEPT13C NMR Spectroscopy -- 11-7. Uses of 13C NMR Spectroscopy -- 11-8. NMR Spectroscopy and Proton Equivalence -- 11-9. Chemical Shifts in 1H NMR Spectroscopy -- 11-10. Integration of 1H NMR Absorptions: Proton Counting -- 11-11. Spin-Spin Splitting in 1H NMR Spectra -- 11-12. More Complex Spin-Spin Splitting Patterns -- 11-13. Uses of 1H NMR Spectroscopy -- Something Extra Magnetic Resonance Imaging (MRI) -- 12. Organohalides: Nucleophilic Substitutions and Eliminations -- 12-1. Names and Structures of Alkyl Halides -- 12-2. Preparing Alkyl Halides from Alkenes: Allylic Bromination -- 12-3. Preparing Alkyl Halides from Alcohols -- 12-4. Reactions of Alkyl Halides: Crignard Reagents -- 12-5. Organometallic Coupling Reactions -- 12-6. Discovery of the Nucleophilic Substitution Reaction -- 12-7. SN2 Reaction -- 12-8. Characteristics of the SN2 Reaction -- 12-9. SN1 Reaction -- 12-10. Characteristics of the SN1 Reaction -- 12-11. Biological Substitution Reactions -- 12-12. Elimination Reactions: Zaitsev's Rule -- 12-13. E2 Reaction and the Deuterium Isotope Effect -- 12-14. E1 and E1cB Reactions -- 12-15. Biological Elimination Reactions -- 12-16. Summary of Reactivity: SN1, SN2, E1, E1cB, and E2 -- Something Extra Naturally Occurring Organohalides -- 13. Alcohols, Phenols, and Thiols; Ethers and Sulfides -- 13-1. Naming Alcohols, Phenols, and Thiols -- 13-2. Properties of Alcohols, Phenols, and Thiols -- 13-3. Preparing Alcohols from Carbonyl Compounds -- 13-4. Reactions of Alcohols -- 13-5. Oxidation of Alcohols and Phenols -- 13-6. Protection of Alcohols -- 13-7. Preparation and Reactions of Thiols -- 13-8. Ethers and Sulfides -- 13-9. Preparing Ethers -- 13-10. Reactions of Ethers -- 13-11. Crown Ethers and lonophores -- 13-12. Preparation and Reactions of Sulfides -- 13-13. Spectroscopy of Alcohols, Phenols, and Ethers -- Something Extra Ethanol: Chemical, Drug, Poison -- A. Preview of Carbonyl Chemistry -- I. Kinds of Carbonyl Compounds -- II. Nature of the Carbonyl Group -- III. General Reactions of Carbonyl Compounds -- IV. Summary -- 14. Aldehydes and Ketones: Nucleophilic Addition Reactions -- 14-1. Naming Aldehydes and Ketones -- 14-2. Preparing Aldehydes and Ketones -- 14-3. Oxidation of Aldehydes -- 14-4. Nucleophilic Addition Reactions of Aldehydes and Ketones -- 14-5. Nucleophilic Addition of H20: Hydration -- 14-6. Nucleophilic Addition of Hydride and Grignard Reagents: Alcohol Formation -- 14-7. Nucleophilic Addition of Amines: Imine and Enamine Formation -- 14-8. Nucleophilic Addition of Alcohols: Acetal Formation -- 14-9. Nucleophilic Addition of Phosphorus Ylides: The Wittig Reaction -- 14-10. Biological Reductions -- 14-11. Conjugate Nucleophilic Addition to α,β-Unsaturated Aldehydes and Ketones -- 14-12. Spectroscopy of Aldehydes and Ketones -- Something Extra Enantioselective Synthesis -- 15. Carboxylic Acids and Nitriles -- 15-1. Naming Carboxylic Acids and Nitriles -- 15-2. Structure and Properties of Carboxylic Acids --

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  • 1 of 1 copy available at University College of the North Libraries.

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Location Call Number / Copy Notes Barcode Shelving Location Holdable? Status Due Date
The Pas Campus Library QD 251.3 .M365 2015 (Text) 58500000073320 Stacks Volume hold Available -
► Summaries & More
► Additional Content
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008131203t20152015ctua 001 0 eng d
010 . ‡a 2013956751
035 . ‡a(DLC) 2013956751
040 . ‡aRRR ‡beng ‡erda ‡cDLC ‡dRRR ‡dYDXCP ‡dOCL ‡dOCLCO ‡dOCL ‡dOCLCO ‡dZWZ ‡dOCLCQ ‡dYDX ‡dNGU ‡dUK7LJ ‡dNhCcYME ‡dMTPK
019 . ‡a911010022 ‡a1156188127
020 . ‡a9781285842912
020 . ‡a128584291X
020 . ‡a128586784X ‡q(paperback)
020 . ‡a9781285867847 ‡q(paperback)
042 . ‡alccopycat
05000. ‡aQD251.3 ‡b.M365 2015
08200. ‡a547 ‡223
1001 . ‡aMcMurry, John, ‡eauthor.
24510. ‡aOrganic chemistry with biological applications / ‡cJohn McMurry, Cornell University.
250 . ‡a3rd Edition.
264 1. ‡aStamford, CT : ‡bCengage Learning, ‡c[2015]
264 4. ‡c©2015
300 . ‡a1 volume (various pagings) : ‡bcolor illustrations ; ‡c25 cm
336 . ‡atext ‡btxt ‡2rdacontent
336 . ‡astill image ‡bsti ‡2rdacontent
337 . ‡aunmediated ‡bn ‡2rdamedia
338 . ‡avolume ‡bnc ‡2rdacarrier
500 . ‡aIncludes index.
520 . ‡a"Renowned for its student-friendly writing style and fresh perspective, John McMurry's ORGANIC CHEMISTRY WITH BIOLOGICAL APPLICATIONS provides full coverage of the foundations of organic chemistry -- enhanced by biological examples throughout. In addition, McMurry discusses the organic chemistry behind biological pathways. The third edition is updated with new problems, illustrations, and essays. Available digital options include the MindTap® Reader and OWLv2, the leading online homework and learning system for chemistry."--Publisher's website.
50500. ‡aMachine generated contents note: ‡g1. ‡tStructure and Bonding -- ‡g1-1. ‡tAtomic Structure: The Nucleus -- ‡g1-2. ‡tAtomic Structure: Orbitals -- ‡g1-3. ‡tAtomic Structure: Electron Configurations -- ‡g1-4. ‡tDevelopment of Chemical Bonding Theory -- ‡g1-5. ‡tDescribing Chemical Bonds: Valence Bond Theory -- ‡g1-6. ‡tSP3 Hybrid Orbitals and the Structure of Methane -- ‡g1-7. ‡tSP3 Hybrid Orbitals and the Structure of Ethane -- ‡g1-8. ‡tSP2 Hybrid Orbitals and the Structure of Ethylene -- ‡g1-9. ‡tSP Hybrid Orbitals and the Structure of Acetylene -- ‡g1-10. ‡tHybridization of Nitrogen, Oxygen, Phosphorus, and Sulfur -- ‡g1-11. ‡tDescribing Chemical Bonds: Molecular Orbital Theory -- ‡g1-12. ‡tDrawing Chemical Structures -- ‡tSomething Extra Organic Foods: Risk versus Benefit -- ‡g2. ‡tPolar Covalent Bonds; Acids and Bases -- ‡g2-1. ‡tPolar Covalent Bonds: Electronegativity -- ‡g2-2. ‡tPolar Covalent Bonds: Dipole Moments -- ‡g2-3. ‡tFormal Charges -- ‡g2-4. ‡tResonance -- ‡g2-5. ‡tRules for Resonance Forms -- ‡g2-6. ‡tDrawing Resonance Forms -- ‡g2-7. ‡tAcids and Bases: The Brønsted-Lowry Definition -- ‡g2-8. ‡tAcid and Base Strength -- ‡g2-9. ‡tPredicting Acid-Base Reactions from pKa Values -- ‡g2-10. ‡tOrganic Acids and Organic Bases -- ‡g2-11. ‡tAcids and Bases: The Lewis Definition -- ‡g2-12. ‡tNoncovalent Interactions between Molecules -- ‡tSomething Extra Alkaloids: From Cocaine to Dental Anesthetics -- ‡g3. ‡tOrganic Compounds: Alkanes and Their Stereochemistry -- ‡g3-1. ‡tFunctional Croups -- ‡g3-2. ‡tAlkanes and Alkane Isomers -- ‡g3-3. ‡tAlkyl Groups -- ‡g3-4. ‡tNaming Alkanes -- ‡g3-5. ‡tProperties of Alkanes -- ‡g3-6. ‡tConformations of Ethane -- ‡g3-7. ‡tConformations of Other Alkanes -- ‡tSomething Extra Gasoline -- ‡g4. ‡tOrganic Compounds: Cycloalkanes and Their Stereochemistry -- ‡g4-1. ‡tNaming Cycloalkanes -- ‡g4-2. ‡tCis-Trans Isomerism in Cycloalkanes -- ‡g4-3. ‡tStability of Cycloalkanes: Ring Strain -- ‡g4-4. ‡tConformations of Cycloalkanes -- ‡g4-5. ‡tConformations of Cyclohexane -- ‡g4-6. ‡tAxial and Equatorial Bonds in Cyclohexane -- ‡g4-7. ‡tConformations of Monosubstituted Cyclohexanes -- ‡g4-8. ‡tConformations of Disubstituted Cyclohexanes -- ‡g4-9. ‡tConformations of Polycyclic Molecules -- ‡tSomething Extra Molecular Mechanics -- ‡g5. ‡tStereochemistry at Tetrahedral Centers -- ‡g5-1. ‡tEnantiomers and the Tetrahedral Carbon -- ‡g5-2. ‡tReason for Handedness in Molecules: Chirality -- ‡g5-3. ‡tOptical Activity -- ‡g5-4. ‡tPasteur's Discovery of Enantiomers -- ‡g5-5. ‡tSequence Rules for Specifying Configuration -- ‡g5-6. ‡tDiastereomers -- ‡g5-7. ‡tMeso Compounds -- ‡g5-8. ‡tRacemic Mixtures and the Resolution of Enantiomers -- ‡g5-9. ‡tReview of Isomerism -- ‡g5-10. ‡tChirality at Nitrogen, Phosphorus, and Sulfur -- ‡g5-11. ‡tProchirality -- ‡g5-12. ‡tChirality in Nature and Chiral Environments -- ‡tSomething Extra Chiral Drugs -- ‡g6. ‡tOverview of Organic Reactions -- ‡g6-1. ‡tKinds of Organic Reactions -- ‡g6-2. ‡tHow Organic Reactions Occur: Mechanisms -- ‡g6-3. ‡tRadical Reactions -- ‡g6-4. ‡tPolar Reactions -- ‡g6-5. ‡tExample of a Polar Reaction: Addition of H2O to Ethylene -- ‡g6-6. ‡tUsing Curved Arrows in Polar Reaction Mechanisms -- ‡g6-7. ‡tDescribing a Reaction: Equilibria, Rates, and Energy Changes -- ‡g6-8. ‡tDescribing a Reaction: Bond Dissociation Energies -- ‡g6-9. ‡tDescribing a Reaction: Energy Diagrams and Transition States -- ‡g6-10. ‡tDescribing a Reaction: Intermediates -- ‡g6-11. ‡tComparison between Biological Reactions and Laboratory Reactions -- ‡tSomething Extra Where Do Drugs Come From? -- ‡g7. ‡tAlkenes and Alkynes -- ‡g7-1. ‡tCalculating the Degree of Unsaturation -- ‡g7-2. ‡tNaming Alkenes and Alkynes -- ‡g7-3. ‡tCis-Trans Isomerism in Alkenes -- ‡g7-4. ‡tAlkene Stereochemistry and the E,Z Designation -- ‡g7-5. ‡tStability of Alkenes -- ‡g7-6. ‡tElectrophilic Addition Reactions of Alkenes -- ‡tWriting Organic Reactions -- ‡g7-7. ‡tOrientation of Electrophilic Addition: Markovnikov's Rule -- ‡g7-8. ‡tCarbocation Structure and Stability -- ‡g7-9. ‡tHammond Postulate -- ‡g7-10. ‡tEvidence for the Mechanism of Electrophilic Additions: Carbocation Rearrangements -- ‡tSomething Extra Terpenes: Naturally Occurring Alkenes -- ‡g8. ‡tReactions of Alkenes and Alkynes j -- ‡g8-1. ‡tPreparing Alkenes: A Preview of Elimination Reactions -- ‡g8-2. ‡tHalogenation of Alkenes -- ‡g8-3. ‡tHalohydrins from Alkenes -- ‡g8-4. ‡tHydration of Alkenes -- ‡g8-5. ‡tReduction of Alkenes: Hydrogenation -- ‡g8-6. ‡tOxidation of Alkenes: Epoxidation -- ‡g8-7. ‡tOxidation of Alkenes: Hydroxylation -- ‡g8-8. ‡tOxidation of Alkenes: Cleavage to Carbonyl Compounds -- ‡g8-9. ‡tAddition of Carbenes to Alkenes: Cyclopropane Synthesis -- ‡g8-10. ‡tRadical Additions to Alkenes: Chain-Growth Polymers -- ‡g8-11. ‡tBiological Additions of Radicals to Alkenes -- ‡g8-12. ‡tConjugated Dienes -- ‡g8-13. ‡tReactions of Conjugated Dienes -- ‡g8-14. ‡tDiels-Alder Cycloaddition Reaction -- ‡g8-15. ‡tReactions of Alkynes -- ‡tSomething Extra--Natural Rubber -- ‡tLearning Reactions -- ‡g9. ‡tAromatic Compounds -- ‡g9-1. ‡tNaming Aromatic Compounds -- ‡g9-2. ‡tStructure and Stability of Benzene -- ‡g9-3. ‡tAromaticity and the Huckel 4n + 2 Rule -- ‡g9-4. ‡tAromatic Ions and Aromatic Heterocycles -- ‡g9-5. ‡tPolycyclic Aromatic Compounds -- ‡g9-6. ‡tReactions of Aromatic Compounds: Electrophilic Substitution -- ‡g9-7. ‡tAlkylation and Acylation of Aromatic Rings: The Friedel--Crafts Reaction -- ‡g9-8. ‡tSubstituent Effects in Electrophilic Substitutions -- ‡g9-9. ‡tNucleophilic Aromatic Substitution -- ‡g9-10. ‡tOxidation and Reduction of Aromatic Compounds -- ‡g9-11. ‡tIntroduction to Organic Synthesis: Polysubstituted Benzenes -- ‡tSomething Extra Aspirin, NSAIDs, and COX-2 Inhibitors -- ‡g10. ‡tStructure Determination: Mass Spectrometry, Infrared Spectroscopy, and Ultraviolet Spectroscopy -- ‡g10-1. ‡tMass Spectrometry of Small Molecules: Magnetic-Sector Instruments -- ‡g10-2. ‡tInterpreting Mass Spectra -- ‡g10-3. ‡tMass Spectrometry of Some Common Functional Groups -- ‡g10-4. ‡tMass Spectrometry in Biological Chemistry: Time-of-Flight (TOF) Instruments -- ‡g10-5. ‡tSpectroscopy and the Electromagnetic Spectrum -- ‡g10-6. ‡tInfrared Spectroscopy -- ‡g10-7. ‡tInterpreting Infrared Spectra -- ‡g10-8. ‡tInfrared Spectra of Some Common Functional Groups -- ‡g10-9. ‡tUltraviolet Spectroscopy -- ‡g10-10. ‡tInterpreting Ultraviolet Spectra: The Effect of Conjugation -- ‡g10-11. ‡tConjugation, Color, and the Chemistry of Vision -- ‡tSomething Extra X-Ray Crystallography -- ‡tStructure Determination: Nuclear Magnetic Resonance Spectroscopy -- ‡g11-1. ‡tNuclear Magnetic Resonance Spectroscopy -- ‡g11-2. ‡tNature of NMR Absorptions -- ‡g11-3. ‡tChemical Shifts -- ‡g11-4. ‡t13C NMR Spectroscopy: Signal Averaging and FT-NMR -- ‡g11-5. ‡tCharacteristics of 13C NMR Spectroscopy -- ‡g11-6. ‡tDEPT13C NMR Spectroscopy -- ‡g11-7. ‡tUses of 13C NMR Spectroscopy -- ‡g11-8. ‡tNMR Spectroscopy and Proton Equivalence -- ‡g11-9. ‡tChemical Shifts in 1H NMR Spectroscopy -- ‡g11-10. ‡tIntegration of 1H NMR Absorptions: Proton Counting -- ‡g11-11. ‡tSpin-Spin Splitting in 1H NMR Spectra -- ‡g11-12. ‡tMore Complex Spin-Spin Splitting Patterns -- ‡g11-13. ‡tUses of 1H NMR Spectroscopy -- ‡tSomething Extra Magnetic Resonance Imaging (MRI) -- ‡g12. ‡tOrganohalides: Nucleophilic Substitutions and Eliminations -- ‡g12-1. ‡tNames and Structures of Alkyl Halides -- ‡g12-2. ‡tPreparing Alkyl Halides from Alkenes: Allylic Bromination -- ‡g12-3. ‡tPreparing Alkyl Halides from Alcohols -- ‡g12-4. ‡tReactions of Alkyl Halides: Crignard Reagents -- ‡g12-5. ‡tOrganometallic Coupling Reactions -- ‡g12-6. ‡tDiscovery of the Nucleophilic Substitution Reaction -- ‡g12-7. ‡tSN2 Reaction -- ‡g12-8. ‡tCharacteristics of the SN2 Reaction -- ‡g12-9. ‡tSN1 Reaction -- ‡g12-10. ‡tCharacteristics of the SN1 Reaction -- ‡g12-11. ‡tBiological Substitution Reactions -- ‡g12-12. ‡tElimination Reactions: Zaitsev's Rule -- ‡g12-13. ‡tE2 Reaction and the Deuterium Isotope Effect -- ‡g12-14. ‡tE1 and E1cB Reactions -- ‡g12-15. ‡tBiological Elimination Reactions -- ‡g12-16. ‡tSummary of Reactivity: SN1, SN2, E1, E1cB, and E2 -- ‡tSomething Extra Naturally Occurring Organohalides -- ‡g13. ‡tAlcohols, Phenols, and Thiols; Ethers and Sulfides -- ‡g13-1. ‡tNaming Alcohols, Phenols, and Thiols -- ‡g13-2. ‡tProperties of Alcohols, Phenols, and Thiols -- ‡g13-3. ‡tPreparing Alcohols from Carbonyl Compounds -- ‡g13-4. ‡tReactions of Alcohols -- ‡g13-5. ‡tOxidation of Alcohols and Phenols -- ‡g13-6. ‡tProtection of Alcohols -- ‡g13-7. ‡tPreparation and Reactions of Thiols -- ‡g13-8. ‡tEthers and Sulfides -- ‡g13-9. ‡tPreparing Ethers -- ‡g13-10. ‡tReactions of Ethers -- ‡g13-11. ‡tCrown Ethers and lonophores -- ‡g13-12. ‡tPreparation and Reactions of Sulfides -- ‡g13-13. ‡tSpectroscopy of Alcohols, Phenols, and Ethers -- ‡tSomething Extra Ethanol: Chemical, Drug, Poison -- ‡gA. ‡tPreview of Carbonyl Chemistry -- ‡gI. ‡tKinds of Carbonyl Compounds -- ‡gII. ‡tNature of the Carbonyl Group -- ‡gIII. ‡tGeneral Reactions of Carbonyl Compounds -- ‡gIV. ‡tSummary -- ‡g14. ‡tAldehydes and Ketones: Nucleophilic Addition Reactions -- ‡g14-1. ‡tNaming Aldehydes and Ketones -- ‡g14-2. ‡tPreparing Aldehydes and Ketones -- ‡g14-3. ‡tOxidation of Aldehydes -- ‡g14-4. ‡tNucleophilic Addition Reactions of Aldehydes and Ketones -- ‡g14-5. ‡tNucleophilic Addition of H20: Hydration -- ‡g14-6. ‡tNucleophilic Addition of Hydride and Grignard Reagents: Alcohol Formation -- ‡g14-7. ‡tNucleophilic Addition of Amines: Imine and Enamine Formation -- ‡g14-8. ‡tNucleophilic Addition of Alcohols: Acetal Formation -- ‡g14-9. ‡tNucleophilic Addition of Phosphorus Ylides: The Wittig Reaction -- ‡g14-10. ‡tBiological Reductions -- ‡g14-11. ‡tConjugate Nucleophilic Addition to α,β-Unsaturated Aldehydes and Ketones -- ‡g14-12. ‡tSpectroscopy of Aldehydes and Ketones -- ‡tSomething Extra Enantioselective Synthesis -- ‡g15. ‡tCarboxylic Acids and Nitriles -- ‡g15-1. ‡tNaming Carboxylic Acids and Nitriles -- ‡g15-2. ‡tStructure and Properties of Carboxylic Acids --
50500. ‡aContents note continued: ‡g15-3. ‡tBiological Acids and the Henderson-Hasselbalch Equation -- ‡g15-4. ‡tSubstituent Effects on Acidity -- ‡g15-5. ‡tPreparing Carboxylic Acids -- ‡g15-6. ‡tReactions of Carboxylic Acids: An Overview -- ‡g15-7. ‡tChemistry of Nitriles -- ‡g15-8. ‡tSpectroscopy of Carboxylic Acids and Nitriles -- ‡tSomething Extra Vitamin C -- ‡g16. ‡tCarboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions -- ‡g16-1. ‡tNaming Carboxylic Acid Derivatives -- ‡g16-2. ‡tNucleophilic Acyl Substitution Reactions -- ‡g16-3. ‡tReactions of Carboxylic Acids -- ‡g16-4. ‡tReactions of Acid Halides -- ‡g16-5. ‡tReactions of Acid Anhydrides -- ‡g16-6. ‡tReactions of Esters -- ‡g16-7. ‡tReactions of Amides -- ‡g16-8. ‡tReactions ofThioesters and Acyl Phosphates: Biological Carboxylic Acid Derivatives -- ‡g16-9. ‡tPolyamides and Polyesters: Step-Growth Polymers -- ‡g16-10. ‡tSpectroscopy of Carboxylic Acid Derivatives -- ‡tSomething Extra Lactam Antibiotics -- ‡g17. ‡tCarbonyl Alpha-Substitution and Condensation Reactions -- ‡g17-1. ‡tKeto-Enol Tautomerism -- ‡g17-2. ‡tReactivity of Enols: a-Substitution Reactions -- ‡g17-3. ‡tAlpha Bromination of Carboxylic Acids -- ‡g17-4. ‡tAcidity of a Hydrogen Atoms: Enolate Ion Formation -- ‡g17-5. ‡tAlkylation of Enolate Ions -- ‡g17-6. ‡tCarbonyl Condensations: The Aldol Reaction -- ‡g17-7. ‡tDehydration of Aldol Products -- ‡g17-8. ‡tIntramolecular Aldol Reactions -- ‡g17-9. ‡tClaisen Condensation Reaction -- ‡g17-10. ‡tIntramolecular Claisen Condensations: The Dieckmann Cyclization -- ‡g17-11. ‡tConjugate Carbonyl Additions: The Michael Reaction -- ‡g17-12. ‡tCarbonyl Condensations with Enamines: The Stork Reaction -- ‡g17-13. ‡tBiological Carbonyl Condensation Reactions -- ‡tSomething Extra Barbiturates -- ‡g18. ‡tAmines and Heterocycles -- ‡g18-1. ‡tNaming Amines -- ‡g18-2. ‡tProperties of Amines -- ‡g18-3. ‡tBasicity of Amines -- ‡g18-4. ‡tBasicity of Arylamines -- ‡g18-5. ‡tBiological Amines and the Henderson-Hasselbalch Equation -- ‡g18-6. ‡tSynthesis of Amines -- ‡g18-7. ‡tReactions of Amines -- ‡g18-8. ‡tHeterocyclic Amines -- ‡g18-9. ‡tFused-Ring Heterocycles -- ‡g18-10. ‡tSpectroscopy of Amines -- ‡tSomething Extra Green Chemistry -- ‡g19. ‡tBiomolecules: Amino Acids. Peptides, and Proteins -- ‡g19-1. ‡tStructures of Amino Acids -- ‡g19-2. ‡tAmino Acids and the Henderson-Hasselbalch Equation: Isoelectric Points -- ‡g19-3. ‡tSynthesis of Amino Acids -- ‡g19-4. ‡tPeptides and Proteins -- ‡g19-5. ‡tAmino Acid Analysis of Peptides -- ‡g19-6. ‡tPeptide Sequencing: The Edman Degradation -- ‡g19-7. ‡tPeptide Synthesis -- ‡g19-8. ‡tProtein Structure -- ‡g19-9. ‡tEnzymes and Coenzymes -- ‡g19-10. ‡tHow Do Enzymes Work? Citrate Synthase -- ‡tSomething Extra The Protein Data Bank -- ‡g20. ‡tAmino Acid Metabolism -- ‡g20-1. ‡tOverview of Metabolism and Biochemical Energy -- ‡g20-2. ‡tCatabolism of Amino Acids: Deamination -- ‡g20-3. ‡tUrea Cycle -- ‡g20-4. ‡tCatabolism of Amino Acids: The Carbon Chains -- ‡g20-5. ‡tBiosynthesis of Amino Acids -- ‡tSomething Extra Visualizing Enzyme Structures -- ‡g21. ‡tBiomolecules: Carbohydrates -- ‡g21-1. ‡tClassifying Carbohydrates -- ‡g21-2. ‡tRepresenting Carbohydrate Stereochemistry: Fischer Projections -- ‡g21-3. ‡tD, L Sugars -- ‡g21-4. ‡tConfigurations of the Aldoses -- ‡g21-5. ‡tCyclic Structures of Monosaccharides: Anomers -- ‡g21-6. ‡tReactions of Monosaccharides -- ‡g21-7. ‡tEight Essential Monosaccharides -- ‡g21-8. ‡tDisaccharides -- ‡g21-9. ‡tPolysaccharides and Their Synthesis -- ‡g21-10. ‡tSome Other Important Carbohydrates -- ‡tSomething Extra Sweetness -- ‡g22. ‡tCarbohydrate Metabolism -- ‡g22-1. ‡tHydrolysis of Complex Carbohydrates -- ‡g22-2. ‡tCatabolism of Glucose: Glycolysis -- ‡g22-3. ‡tConversion of Pyruvate to Acetyl CoA -- ‡g22-4. ‡tCitric Acid Cycle -- ‡g22-5. ‡tBiosynthesis of Glucose: Gluconeogenesis -- ‡tSomething Extra Influenza Pandemics -- ‡g23. ‡tBiomolecules: Lipids and Their Metabolism -- ‡g23-1. ‡tWaxes, Fats, and Oils -- ‡g23-2. ‡tSoap -- ‡g23-3. ‡tPhospholipids -- ‡g23-4. ‡tCatabolism of Triacylglycerols: The Fate of Glycerol -- ‡g23-5. ‡tCatabolism of Triacylglycerols: β-Oxidation -- ‡g23-6. ‡tBiosynthesis of Fatty Acids -- ‡g23-7. ‡tProstaglandins and Other Eicosanoids -- ‡g23-8. ‡tTerpenoids -- ‡g23-9. ‡tSteroids -- ‡g23-10. ‡tBiosynthesis of Steroids -- ‡g23-11. ‡tSome Final Comments on Metabolism -- ‡tSomething Extra Statin Drugs -- ‡g24. ‡tBiomolecules: Nucleic Acids and Their Metabolism j -- ‡g24-1. ‡tNucleotides and Nucleic Acids -- ‡g24-2. ‡tBase Pairing in DNA: The Watson-Crick Model -- ‡g24-3. ‡tReplication of DNA -- ‡g24-4. ‡tTranscription of DNA -- ‡g24-5. ‡tTranslation of RNA: Protein Biosynthesis -- ‡g24-6. ‡tDNA Sequencing -- ‡g24-7. ‡tDNA Synthesis -- ‡g24-8. ‡tPolymerase Chain Reaction -- ‡g24-9. ‡tCatabolism of Nucleotides -- ‡g24-10. ‡tBiosynthesis of Nucleotides -- ‡tSomething Extra DNA Fingerprinting -- ‡ge25. ‡tSecondary Metabolites: An Introduction to Natural Products Chemistry -- ‡g25-1. ‡tClassifying Natural Products -- ‡g25-2. ‡tBiosynthesis of Pyridoxal Phosphate -- ‡g25-3. ‡tBiosynthesis of Morphine -- ‡g25-4. ‡tBiosynthesis of Erythromycin -- ‡tSomething Extra Bioprospecting: Hunting for Natural Products -- ‡ge26. ‡tOrbitals and Organic Chemistry: Pericyclic Reactions -- ‡g26-1. ‡tMolecular Orbitals of Conjugated Pi Systems -- ‡g26-2. ‡tElectrocyclic Reactions -- ‡g26-3. ‡tStereochemistry of Thermal Electrocyclic Reactions -- ‡g26-4. ‡tPhotochemical Electrocyclic Reactions -- ‡g26-5. ‡tCycloaddition Reactions -- ‡g26-6. ‡tStereochemistry of Cycloadditions -- ‡g26-7. ‡tSigmatropic Rearrangements -- ‡g26-8. ‡tSome Examples of Sigmatropic Rearrangements -- ‡g26-9. ‡tSummary of Rules for Pericyclic Reactions -- ‡tSomething Extra Vitamin P. the Sunshine Vitamin -- ‡ge27. ‡tSynthetic Polymers -- ‡g27-1. ‡tChain-Growth Polymers -- ‡g27-2. ‡tStereochemistry of Polymerization: Ziegler-Natta Catalysts -- ‡g27-3. ‡tCopolymers -- ‡g27-4. ‡tStep-Growth Polymers -- ‡g27-5. ‡tOlefin Metathesis Polymerization -- ‡g27-6. ‡tPolymer Structure and Physical Properties -- ‡tBiodegradable Polymers -- ‡tAppendices -- ‡gA. ‡tNomenclature of Polyfunctional Organic Compounds -- ‡gB. ‡tAcidity Constants for Some Organic Compounds -- ‡gC. ‡tGlossary -- ‡gD. ‡tAnswers to In-Text Problems.
650 0. ‡aChemistry, Organic ‡vTextbooks.
650 0. ‡aBiochemistry ‡vTextbooks.
852 . ‡b58500000073320 ‡cQD251.3 .M365 2015 ‡e465.43 ‡f30100 ‡lStacks ‡mbook ‡nordered for Selvin Peter GOBI ‡oMTPK ‡q1 ‡sIn process
905 . ‡uNA978233
901 . ‡a128236489 ‡bAUTOGEN ‡c128236489 ‡tbiblio ‡sYPB
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