Cover Image

Organic Chemistry.

Bibliographic Details
Main Author: McMurry, John E.
Format: eBook
Language:English
Published: Mason, OH : Cengage, 2016.
Edition:9th ed.
Subjects:
Chemistry, Organic-Textbooks.
Electronic books.
Online Access:View fulltext via EzAccess
LEADER 11159nam a22004813i 4500
001 EBC6351202
003 MiAaPQ
005 20210318061024.0
006 m o d |
007 cr cnu||||||||
008 210318s2015 xx o ||||0 eng d
020 |a 9781305686465  |q (electronic bk.) 
020 |z 9781305080485 
035 |a (MiAaPQ)EBC6351202 
035 |a (Au-PeEL)EBL6351202 
035 |a (OCoLC)970629261 
040 |a MiAaPQ  |b eng  |e rda  |e pn  |c MiAaPQ  |d MiAaPQ 
050 4 |a QD251.3 .M368 2016 
082 0 |a 547 
100 1 |a McMurry, John E. 
245 1 0 |a Organic Chemistry. 
250 |a 9th ed. 
264 1 |a Mason, OH :  |b Cengage,  |c 2016. 
264 4 |c ©2016. 
300 |a 1 online resource (1518 pages) 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
505 0 |a Intro -- Brief Contents -- Detailed Contents -- Preface -- Ch 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 -- Summary -- Ch 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 Bronsted-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 -- Summary -- Ch 3: Organic Compounds: Alkanes and Their Stereochemistry -- 3-1: Functional Groups -- 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 -- Summary -- Ch 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. 
505 8 |a 4-7: Conformations of Monosubstituted Cyclohexanes -- 4-8: Conformations of Disubstituted Cyclohexanes -- 4-9: Conformations of Polycyclic Molecules -- Summary -- Ch 5: Stereochemistry at Tetrahedral Centers -- 5-1: Enantiomers and the Tetrahedral Carbon -- 5-2: The 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: A Review of Isomerism -- 5-10: Chirality at Nitrogen, Phosphorus, and Sulfur -- 5-11: Prochirality -- 5-12: Chirality in Nature and Chiral Environments -- Summary -- Ch 6: An 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: An Example of a Polar Reaction: Addition of HBr 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: A Comparison between Biological Reactions and Laboratory Reactions -- Summary -- Practice Your Scientific Analysis and Reasoning I: The Chiral Drug Thalidomide -- Ch 7: Alkenes: Structure and Reactivity -- 7-1: Industrial Preparation and Use of Alkenes -- 7-2: Calculating Degree of Unsaturation -- 7-3: Naming Alkenes -- 7-4: Cis-Trans Isomerism in Alkenes -- 7-5: Alkene Stereochemistry and the E,Z Designation -- 7-6: Stability of Alkenes -- 7-7: Electrophilic Addition Reactions of Alkenes -- 7-8: Orientation of Electrophilic Additions: Markovnikov's Rule -- 7-9: Carbocation Structure and Stability. 
505 8 |a 7-10: The Hammond Postulate -- 7-11: Evidence for the Mechanism of Electrophilic Additions: Carbocation Rearrangements -- Summary -- Ch 8: Alkenes: Reactions and Synthesis -- 8-1: Preparing Alkenes: A Preview of Elimination Reactions -- 8-2: Halogenation of Alkenes: Addition of X2 -- 8-3: Halohydrins from Alkenes: Addition of HOX -- 8-4: Hydration of Alkenes: Addition of H2O by Oxymercuration -- 8-5: Hydration of Alkenes: Addition of H2O by Hydroboration -- 8-6: Reduction of Alkenes: Hydrogenation -- 8-7: Oxidation of Alkenes: Epoxidation and 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: Reaction Stereochemistry: Addition of H2O to an Achiral Alkene -- 8-13: Reaction Stereochemistry: Addition of H2O to a Chiral Alkene -- Summary -- Ch 9: Alkynes: An Introduction to Organic Synthesis -- 9-1: Naming Alkynes -- 9-2: Preparation of Alkynes: Elimination Reactions of Dihalides -- 9-3: Reactions of Alkynes: Addition of HX and X2 -- 9-4: Hydration of Alkynes -- 9-5: Reduction of Alkynes -- 9-6: Oxidative Cleavage of Alkynes -- 9-7: Alkyne Acidity: Formation of Acetylide Anions -- 9-8: Alkylation of Acetylide Anions -- 9-9: An Introduction to Organic Synthesis -- Summary -- Ch 10: Organohalides -- 10-1: Names and Structures of Alkyl Halides -- 10-2: Preparing Alkyl Halides from Alkanes: Radical Halogenation -- 10-3: Preparing Alkyl Halides from Alkenes: Allylic Bromination -- 10-4: Stability of the Allyl Radical: Resonance Revisited -- 10-5: Preparing Alkyl Halides from Alcohols -- 10-6: Reactions of Alkyl Halides: Grignard Reagents -- 10-7: Organometallic Coupling Reactions -- 10-8: Oxidation and Reduction in Organic Chemistry -- Summary. 
505 8 |a Ch 11: Reactions of Alkyl Halides: Nucleophilic Substitutions and Eliminations -- 11-1: The Discovery of Nucleophilic Substitution Reactions -- 11-2: The SN2 Reaction -- 11-3: Characteristics of the SN2 Reaction -- 11-4: The SN1 Reaction -- 11-5: Characteristics of the SN1 Reaction -- 11-6: Biological Substitution Reactions -- 11-7: Elimination Reactions: Zaitsev's Rule -- 11-8: The E2 Reaction and the Deuterium Isotope Effect -- 11-9: The E2 Reaction and Cyclohexane Conformation -- 11-10: The E1 and E1cB Reactions -- 11-11: Biological Elimination Reactions -- 11-12: A Summary of Reactivity: SN1, SN2, E1, E1cB, and E2 -- Summary -- Practice Your Scientific Analysis and Reasoning II: From Mustard Gas to Alkylating Anticancer Drugs -- Ch 12: Structure Determination: Mass Spectrometry and Infrared Spectroscopy -- 12-1: Mass Spectrometry of Small Molecules: Magnetic-Sector Instruments -- 12-2: Interpreting Mass Spectra -- 12-3: Mass Spectrometry of Some Common Functional Groups -- 12-4: Mass Spectrometry in Biological Chemistry: Time-of-Flight (TOF) Instruments -- 12-5: Spectroscopy and the Electromagnetic Spectrum -- 12-6: Infrared Spectroscopy -- 12-7: Interpreting Infrared Spectra -- 12-8: Infrared Spectra of Some Common Functional Groups -- Summary -- Ch 13: Structure Determination: Nuclear Magnetic Resonance Spectroscopy -- 13-1: Nuclear Magnetic Resonance Spectroscopy -- 13-2: The Nature of NMR Absorptions -- 13-3: The Chemical Shift -- 13-4: Chemical Shifts in 1H NMR Spectroscopy -- 13-5: Integration of 1H NMR Absorptions: Proton Counting -- 13-6: Spin-Spin Splitting in 1H NMR Spectra -- 13-7: 1H NMR Spectroscopy and Proton Equivalence -- 13-8: More Complex Spin-Spin Splitting Patterns -- 13-9: Uses of 1H NMR Spectroscopy -- 13-10: 13C NMR Spectroscopy: Signal Averaging and FT-NMR -- 13-11: Characteristics of 13C NMR Spectroscopy. 
505 8 |a 13-12: DEPT 13C NMR Spectroscopy -- 13-13: Uses of 13C NMR Spectroscopy -- Summary -- Ch 14: Conjugated Compounds and Ultraviolet Spectroscopy -- 14-1: Stability of Conjugated Dienes: Molecular Orbital Theory -- 14-2: Electrophilic Additions to Conjugated Dienes: Allylic Carbocations -- 14-3: Kinetic versus Thermodynamic Control of Reactions -- 14-4: The Diels-Alder Cycloaddition Reaction -- 14-5: Characteristics of the Diels-Alder Reaction -- 14-6: Diene Polymers: Natural and Synthetic Rubbers -- 14-7: Ultraviolet Spectroscopy -- 14-8: Interpreting Ultraviolet Spectra: The Effect of Conjugation -- 14-9: Conjugation, Color, and the Chemistry of Vision -- Summary -- Practice Your Scientific Analysis and Reasoning III: Photodynamic Therapy (PDT) -- Ch 15: Benzene and Aromaticity -- 15-1: Naming Aromatic Compounds -- 15-2: Structure and Stability of Benzene -- 15-3: Aromaticity and the Huckel 4n + 2 Rule -- 15-4: Aromatic Ions -- 15-5: Aromatic Heterocycles: Pyridine and Pyrrole -- 15-6: Polycyclic Aromatic Compounds -- 15-7: Spectroscopy of Aromatic Compounds -- Summary -- Ch 16: Chemistry of Benzene: Electrophilic Aromatic Substitution -- 16-1: Electrophilic Aromatic Substitution Reactions: Bromination -- 16-2: Other Aromatic Substitutions -- 16-3: Alkylation and Acylation of Aromatic Rings: The Friedel-Crafts Reaction -- 16-4: Substituent Effects in Electrophilic Substitutions -- 16-5: Trisubstituted Benzenes: Additivity of Effects -- 16-6: Nucleophilic Aromatic Substitution -- 16-7: Benzyne -- 16-8: Oxidation of Aromatic Compounds -- 16-9: Reduction of Aromatic Compounds -- 16-10: Synthesis of Polysubstituted Benzenes -- Summary -- Ch 17: Alcohols and Phenols -- 17-1: Naming Alcohols and Phenols -- 17-2: Properties of Alcohols and Phenols -- 17-3: Preparation of Alcohols: A Review -- 17-4: Alcohols from Carbonyl Compounds: Reduction. 
505 8 |a 17-5: Alcohols from Carbonyl Compounds: Grignard Reaction. 
526 0 |a AS120 - Diploma in Science  |z Syllabus Programme 
588 |a Description based on publisher supplied metadata and other sources. 
590 |a Electronic reproduction. Ann Arbor, Michigan : ProQuest Ebook Central, 2021. Available via World Wide Web. Access may be limited to ProQuest Ebook Central affiliated libraries.  
650 0 |a Chemistry, Organic-Textbooks. 
655 4 |a Electronic books. 
776 0 8 |i Print version:  |a McMurry, John E.  |t Organic Chemistry  |d Mason, OH : Cengage,c2015  |z 9781305080485 
797 2 |a ProQuest (Firm) 
856 4 0 |u https://ezaccess.library.uitm.edu.my/login?url=https://ebookcentral.proquest.com/lib/uitm-ebooks/detail.action?docID=6351202  |z View fulltext via EzAccess 
966 0 |a 2021  |b ProQuest Ebook Central  |c UiTM Library  |d Mohd Fadhli Samsudin  |e Faculty of Applied Sciences  |f ProQuest 

Similar Items