Organic Chemistry (9th Edition) - 9th Edition - by Leroy G. Wade, Jan W. Simek - ISBN 9780321971371

Organic Chemistry (9th Edition)
9th Edition
Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
ISBN: 9780321971371

Solutions for Organic Chemistry (9th Edition)

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Chapter 1.16 - Drawing Three-dimensional MoleculesChapter 1.17 - General Rules Of Hybridization And GeometryChapter 1.18B - Rigidity Of Double BondsChapter 1.19B - StereoisomersChapter 2 - Acids And Bases; Functional GroupsChapter 2.1A - Bond Dipole MomentsChapter 2.1B - Molecular Dipole MomentsChapter 2.2C - Hydrogen BondingChapter 2.3 - Polarity Effects On SolubilitiesChapter 2.4 - Arrhenius Acids And BasesChapter 2.6A - Acids StrengthChapter 2.7 - Equilibrium Positions Of Acid-base ReactionsChapter 2.8 - Solvent Effects On Acidity And BasicityChapter 2.10 - Inductive Effects On AcidityChapter 2.11 - Hybridization Effects On AcidityChapter 2.12 - Resonance Effects On Acidity And BasicityChapter 2.14 - The Curved-arrow FormalismChapter 2.15D - Aromatic HydrocarbonsChapter 2.16D - Carboxylic AcidsChapter 2.17C - NitrilesChapter 3 - Structure And Stereochemistry Of AlkanesChapter 3.2 - Molecular Formulas Of AlkanesChapter 3.3B - Iupac Or Systematic NamesChapter 3.4C - Melting Points Of AlkanesChapter 3.7B - Conformations Of EthaneChapter 3.7C - Conformations Of PropaneChapter 3.8B - Steric StrainChapter 3.9 - Conformations Of Higher AlkanesChapter 3.10C - Nomenclature Of CycloalkanesChapter 3.11 - Cis-trans Isomerism In CycloalkanesChapter 3.12B - CyclopropaneChapter 3.12C - CyclobutaneChapter 3.13B - Axial And Equatorial PositionsChapter 3.14 - Conformations Of Monosubstituted CyclohexanesChapter 3.15 - Conformations Of Disubstituted CyclohexanesChapter 3.15A - Substituents Of Different SizesChapter 3.15B - Extremely Bulky GroupsChapter 3.16A - Nomenclature Of Bicyclic AlkanesChapter 3.16B - Cis- And Trans-decalinChapter 4 - The Study Of Chemical ReactionsChapter 4.3A - The Initiation Step: Generation Of RadicalsChapter 4.3B - Propagation StepsChapter 4.3C - Termination ReactionsChapter 4.4 - Equilibrium Constants And Free EnergyChapter 4.5B - EntropyChapter 4.7 - Enthalpy Changes In ChlorinationChapter 4.8 - Kinetics And The Rate EquationChapter 4.10 - Transition StatesChapter 4.12 - Temperature Dependence Of HalogenationChapter 4.13A - Chlorination Of Propane: Product RatiosChapter 4.13B - Free-radical StabilitiesChapter 4.14 - Hammond's PostulateChapter 4.15 - Radical InhibitorsChapter 4.16A - CarbocationsChapter 4.16B - Free RadicalsChapter 4.16C - CarbanionsChapter 4.16D - CarbenesChapter 5 - StereochemistryChapter 5.2 - ChiralityChapter 5.2A - Chirality And Enantiomers In Organic MoleculesChapter 5.2B - Asymmetric Carbon Atoms, Chiral Centers, And StereocentersChapter 5.2C - Mirror Planes Of SymmetryChapter 5.3 - (r) And (s) Nomenclature Of Asymmetric Carbon AtomsChapter 5.4D - Specific RotationChapter 5.5 - Biological Discrimination Of EnantiomersChapter 5.7 - Enantiomeric Excess And Optical PurityChapter 5.8 - Chirality Of Conformationally Mobile SystemsChapter 5.9B - AllenesChapter 5.10A - Drawing Fischer ProjectionsChapter 5.10B - Drawing Mirror Images Of Fischer ProjectionsChapter 5.10C - Assigning (r) And (s) Configurations From Fischer ProjectionsChapter 5.11C - Diastereomers Of Molecules With Two Or More Chiral CentersChapter 5.13 - Meso CompoundsChapter 5.15 - Physical Properties Of DiastereomersChapter 5.16A - Chemical Resolution Of EnantiomersChapter 6 - Alkyl Halides; Nucleophilic SubstitutionChapter 6.1 - IntroductionChapter 6.2 - Nomenclature Of Alkyl HalidesChapter 6.3E - PesticidesChapter 6.4 - Structure Of Alkyl HalidesChapter 6.5A - Boiling PointsChapter 6.5B - DensitiesChapter 6.6B - Allylic BrominationChapter 6.7 - Reactions Of Alkyl Halides: Substitution And EliminationChapter 6.8 - Biomolecular Nucleophilic Substitution: The Sn2 ReactionChapter 6.9 - Generality Of The Sn2 ReactionChapter 6.10A - Steric Effects Of NucleophilicityChapter 6.11A - Leaving-group Effects On The SubstrateChapter 6.11B - Steric Effects On The SubstrateChapter 6.12 - Stereochemistry Of The Sn2 ReactionChapter 6.13 - Unimolecular Nucleophilic Substitution: The Sn1 ReactionChapter 6.13B - Leaving-group EffectsChapter 6.15 - Rearrangements In Sn1 ReactionsChapter 6.16 - Comparison Of Sn1 And Sn2 ReactionsChapter 7 - Structure And Synthesis Of Alkenes; EliminationChapter 7.3A - Elements Of Unsaturation In HydrocarbonsChapter 7.3B - Elements Of Unsaturation With HeteroatomsChapter 7.4 - Nomenclature Of AlkenesChapter 7.5B - E-z NomenclatureChapter 7.6 - Commercial Importance Of AlkenesChapter 7.7B - PolarityChapter 7.8B - Substitution EffectsChapter 7.8C - Energy Difference In Cis-trans IsomersChapter 7.8E - Bredt's RuleChapter 7.8F - Enhanced Stability Of Conjugated Double BondsChapter 7.10 - Unimolecular Elimination: The E1 ReactionChapter 7.10A - Competition Between The E1 And Sn1Chapter 7.10C - Rearrangements In E1 ReactionsChapter 7.11 - Positional Orientation Of Elimination: Zaitsev's RuleChapter 7.12 - Bimolecular Elimination: The E2 ReactionChapter 7.13 - Bulky Bases In E2 Eliminations; Hofmann OrientationChapter 7.14B - Stereospecific E2 ReactionsChapter 7.15 - E2 Reactions In Cyclohexane SystemsChapter 7.16 - Comparison Of E1 And E2 Elimination MechanismsChapter 7.17B - Unimolecular Substitution Versus Elimination (weak Base Or Nucleophile)Chapter 7.18 - Alkene Synthesis By Dehydration Of AlcoholsChapter 7.19B - Dehydrogenation Of AlkanesChapter 8 - Reactions Of AlkenesChapter 8.3A - Orientation Of Addition: Markovnikov's RuleChapter 8.3B - Free-radical Addition Of Hbr: Anti-markovnikov AdditionChapter 8.4B - Orientation Of HydrationChapter 8.6 - Alkoxymercuration-demercurationChapter 8.7A - Mechanism Of HydroborationChapter 8.7C - Stereochemistry Of HydroborationChapter 8.8B - Stereochemistry Of Halogen AdditionChapter 8.9 - Formation Of HalohydrinsChapter 8.10 - Catalytic Hydrogenation Of AlkenesChapter 8.11A - The Simmons-smith ReactionChapter 8.11B - Formation Of Carbenes By Alpha EliminationChapter 8.12 - Epoxidation Of AlkenesChapter 8.13 - Acid-catalyzed Opening Of EpoxidesChapter 8.14C - Choosing A ReagentChapter 8.15B - OzonolysisChapter 8.15C - Comparison Of Permanganate Cleavage And OzonolysisChapter 8.16A - Cationic PolymerizationChapter 8.16B - Free-radical PolymerizationChapter 8.16C - Anionic PolymerizationChapter 8.17B - Mechanism Of Olefin MetathesisChapter 9 - AlkynesChapter 9.1 - IntroductionChapter 9.2 - Nomenclature Of AlkynesChapter 9.4B - Manufacture Of AcetyleneChapter 9.6 - Acidity Of Alkynes; Formation Of Acetylide IonsChapter 9.7A - Alkylation Of Acetylide IonsChapter 9.7B - Addition Of Acetylide Ions To Carbonyl GroupsChapter 9.8 - Synthesis Of Alkynes By Elimination ReactionsChapter 9.9C - Metal-ammonia Reduction To Trans AlkenesChapter 9.9D - Addition Of HalogensChapter 9.9E - Addition Of Hydrogen HalidesChapter 9.9F - Hydration Of Alkynes To Ketones And AldehydesChapter 9.10A - Permanganate OxidationsChapter 9.10B - OzonolysisChapter 10 - Structure And Synthesis Of AlcoholsChapter 10.3A - Iupac Names ("alkanol" Names)Chapter 10.3B - Common Names Of AlcoholsChapter 10.3C - Names Of DiolsChapter 10.4B - Solubility Properties Of AlcoholsChapter 10.6A - Effects On AcidityChapter 10.6C - Acidity Of PhenolsChapter 10.8B - Organolithium ReagentsChapter 10.9A - Addition Of Formaldehdye: Formation Of Primary AlcoholsChapter 10.9B - Addition To Aldehydes: Formation Of Secondary AlcoholsChapter 10.9C - Addition To Ketones: Formation Of Tertiary AlcoholsChapter 10.9D - Addition To Acid Chlorides And EstersChapter 10.9E - Ring-opening With Ethylene OxideChapter 10.9F - Lithium DialkylcupratesChapter 10.10A - Reactions With Acidic CompoundsChapter 10.10B - Reactions With Electrophilic Multiple BondsChapter 10.11B - Uses Of Lithium Aluminium HydrideChapter 10.12 - Thiols (mercaptans)Chapter 11 - Reactions Of AlcoholsChapter 11.1 - Oxidation States Of Alcohols And Related Functional GroupsChapter 11.2C - Resistance Of Tertiary Alcohols To OxidationChapter 11.3 - Additional Methods For Oxidizing AlcoholsChapter 11.4 - Biological Oxidation Of AlcoholsChapter 11.5 - Alcohols As Nucleophiles And Electrophiles; Formation Of TosylatesChapter 11.6 - Reduction Of AlcoholsChapter 11.7A - Reactions With Hydrobromic AcidChapter 11.7B - Reactions With Hydrochloric AcidChapter 11.7C - Limitations On The Use Of Hydrohalic Acids With AlcoholsChapter 11.8 - Reactions Of Alcohols With Phosphorus HalidesChapter 11.9 - Reactions Of Alcohols With Thionyl ChlorideChapter 11.10A - Formation Of AlkenesChapter 11.10B - Bimolecular Condensation To Form Ethers (industrial)Chapter 11.11A - The Pinacol RearrangementChapter 11.11B - Periodic Acid Cleavage Of GlycolsChapter 11.12 - Esterification Of AlcoholsChapter 11.13A - Sulfate EstersChapter 11.14 - Reactions Of AlkoxidesChapter 12 - Infrared Spectroscopy And Mass SpectrometryChapter 12.3 - The Infrared RegionChapter 12.5 - Ir-active And Ir-inactive VibrationsChapter 12.7C - Interpreting The Ir Spectra Of HydrocarbonsChapter 12.9A - Simple Ketones, Aldehydes, And AcidsChapter 12.10 - Characteristic Absorptions Of Cn BondsChapter 12.12 - Reading And Interpreting Ir Spectra (solved Problems)Chapter 12.14B - Use Of Heavier Isotope PeaksChapter 12.15A - Mass Spectra Of AlkanesChapter 12.15B - Fragmentation Giving Resonance-stabilized CationsChapter 12.15C - Fragmentation Splitting Out A Small Molecule; Mass Spectra Of AlcoholsChapter 13 - Nuclear Magnetic Resonance SpectroscopyChapter 13.5A - Measurement Of Chemical ShiftsChapter 13.5B - Characteristic Values Of Chemical ShiftsChapter 13.6 - The Number Of SignalsChapter 13.7 - Areas Of The PeaksChapter 13.8C - The Range Of Magnetic CouplingChapter 13.8D - Coupling ConstantsChapter 13.9 - Complex SplittingChapter 13.10 - Stereochemical Nonequivalence Of ProtonsChapter 13.11B - Fast Proton TransfersChapter 13.12E - Spin-spin SplittingChapter 13.12F - Dept 13c NmrChapter 13.13 - Interpreting Carbon Nmr SpectraChapter 13.14 - Nuclear Magnetic Resonance ImagingChapter 14 - Ethers, Epoxides, And ThioethersChapter 14.2C - Ethers As Polar SolventsChapter 14.2D - Stable Complexes Of Ethers With ReagentsChapter 14.3B - Iupac Names (alkoxy Alkane Names)Chapter 14.3C - Nomenclature Of Cyclic EthersChapter 14.4 - Spectroscopy Of EthersChapter 14.5 - The Williamson Ether SynthesisChapter 14.6 - Synthesis Of Ethers By Alkoxymercuration-demercurationChapter 14.7 - Industrial Synthesis: Bimolecular Condensation Of AlcoholsChapter 14.8 - Cleavage Of Ethers By Hbr And HiChapter 14.10A - Thioethers (sulfides)Chapter 14.10B - Silyl Ethers As Alcohol-protecting GroupsChapter 14.11B - Base-promoted Cyclization Of HalohydrinsChapter 14.12 - Acid-catalyzed Ring Opening Of EpoxidesChapter 14.13 - Base-catalyzed Ring Opening Of EpoxidesChapter 14.14 - Orientation Of Epoxide Ring OpeningChapter 14.15 - Reactions Of Epoxides With Grignard And Organolithium ReagentsChapter 15 - Conjugated Systems, Orbital Symmetry, And Ultraviolet SpectroscopyChapter 15.2 - Stabilities Of DienesChapter 15.4 - Allylic CationsChapter 15.5 - 1,2- And 1,4-addition Of Conjugated DienesChapter 15.6 - Kinetic Versus Thermodynamic Control In The Addition Of Hbr To Buta-1,3-dieneChapter 15.7 - Allylic RadicalsChapter 15.9 - Electronic Configurations Of The Allyl Radical, Cation, And AnionChapter 15.10 - Sn2 Displacement Reactions Of Allylic Halides And TosylatesChapter 15.11 - The Diels-alder ReactionChapter 15.11A - Stereochemical Requirements Of The Diels-alder Transition StateChapter 15.11B - Diels-alder Reactions Using Unsymmetrical ReagentsChapter 15.12C - Photochemical Induction Of CycloadditionsChapter 15.13C - Obtaining An Ultraviolet SpectrumChapter 15.13D - Interpreting Uv-visible SpectraChapter 15.14 - Colored Organic CompoundsChapter 16 - Aromatic CompoundsChapter 16.2 - The Structure And Properties Of BenzeneChapter 16.4 - The Molecular Orbital Picture Of CyclobutadieneChapter 16.6 - Huckel's RuleChapter 16.7 - Molecular Orbital Derivation Of Huckel's RuleChapter 16.8A - The Cyclopentadienyl IonsChapter 16.8C - The Cyclooctatetraene DianionChapter 16.9B - PyrroleChapter 16.9C - Pyrimidine And ImidazoleChapter 16.9D - Furan And ThiopheneChapter 16.10 - Polynuclear Aromatic HydrocarbonsChapter 16.12 - Fused Heterocyclic CompoundsChapter 16.13 - Nomenclature Of Benzene DerivativesChapter 16.15 - Spectroscopy Of Aromatic CompoundsChapter 17 - Reactions Of Aromatic CompoundsChapter 17.1 - Electrophilic Aromatic SubstitutionChapter 17.2 - Halogenation Of BenzeneChapter 17.3 - Nitration Of BenzeneChapter 17.4 - Sulfonation Of BenzeneChapter 17.6A - Alkyl GroupsChapter 17.6B - Substituents With Nonbonding ElectronsChapter 17.7 - Deactivating, Meta-directing SubstituentsChapter 17.8 - Halogen Substituents: Deactivating, But Ortho, Para-directingChapter 17.9 - Effects Of Multiple Substituents On Electrophilic Aromatic SubstitutionChapter 17.10 - The Friedel-crafts AlkylationChapter 17.11C - The Gatterman-koch Formylation: Synthesis Of BenzaldehydesChapter 17.12A - The Addition-elimination MechanismChapter 17.12B - The Benzyne Mechanism: Elimination-additionChapter 17.13A - Couplings Using Organocuprate ReagentsChapter 17.13B - The Heck ReactionChapter 17.13C - The Suzuki Reaction (suzuki Coupling)Chapter 17.14C - Birch ReductionChapter 17.15A - Permanganate OxidationChapter 17.15B - Side-chain HalogenationChapter 17.15C - Nucleophilic Substitution At The Benzylic PositionChapter 17.16A - Oxidation Of Phenols To QuinonesChapter 17.16B - Electrophilic Aromatic Substitution Of PhenolsChapter 18 - Ketones And AldehydesChapter 18.3 - Nomenclature Of Ketones And AldehydesChapter 18.5D - Mass Spectra Of Ketones And AldehydesChapter 18.5E - Ultraviolet Spectra Of Ketones And AldehydesChapter 18.7D - Ketones And Aldehydes From Hydration Of AlkynesChapter 18.8 - Synthesis Of Ketones From Carboxylic AcidsChapter 18.9 - Synthesis Of Ketones And Aldehydes From NitrilesChapter 18.10 - Synthesis Of Aldehydes And Ketones From Acid Chlorides And EstersChapter 18.11 - Reactions Of Ketones And Aldehydes: Introduction To Nucleophilic AdditionChapter 18.12 - Hydration Of Ketones And AldehydesChapter 18.13 - Formation Of CyanohydrinsChapter 18.14 - Formation Of IminesChapter 18.15 - Condensations With Hydroxylamine And HydrazinesChapter 18.16 - Formation Of AcetalsChapter 18.17 - Use Of Acetals As Protecting GroupsChapter 18.18 - The Wittig ReactionChapter 18.19 - Oxidation Of AldehydesChapter 18.20C - Deoxygenation Of Ketones And AldehydesChapter 19 - AminesChapter 19.2A - Common NamesChapter 19.2B - Iupac NamesChapter 19.3 - Structure Of AminesChapter 19.4 - Physical Properties Of AminesChapter 19.6 - Factors That Affect Amine BasicityChapter 19.8A - Infrared SpectroscopyChapter 19.8C - Carbon Nmr SpectroscopyChapter 19.8D - Mass SpectrometryChapter 19.10B - Electrophilic Aromatic Substitution Of PyridineChapter 19.10C - Nucleophilic Aromatic Substitution Of PyridineChapter 19.11 - Alkylation Of Amines By Alkyl HalidesChapter 19.12 - Acylation Of Amines By Acid ChloridesChapter 19.13 - Formation Of SulfonamidesChapter 19.14 - Amines Are Leaving Groups: The Hofmann EliminationChapter 19.15 - Oxidation Of Amines; The Cope EliminationChapter 19.16 - Reactions Of Amines With Nitrous AcidChapter 19.17 - Reactions Of Arenediazonium SaltsChapter 19.18 - Synthesis Of Amines By Reductive AminationChapter 19.19 - Synthesis Of Amines By Acylation-reductionChapter 19.20A - Direct Alkylation And Gabriel SynthesisChapter 19.20B - Reduction Of Azides And NitrilesChapter 19.20C - Reduction Of Nitro CompoundsChapter 20 - Carboxylic AcidsChapter 20.2C - Nomenclature Of Dicarboxylic AcidsChapter 20.4B - Substituent Effects On AcidityChapter 20.5 - Salts Of Carboxylic AcidsChapter 20.7A - Infrared SpectroscopyChapter 20.7B - Nmr SpectroscopyChapter 20.7D - Mass SpectrometryChapter 20.10 - Condensation Of Acids And Alcohols: The Fischer EsterificationChapter 20.12 - Condensation Of Acids With Amines: Direct Synthesis Of AmidesChapter 20.13 - Reduction Of Carboxylic AcidsChapter 20.14 - Alkylation Of Carboxylic Acids To Form KetonesChapter 20.15 - Synthesis And Use Of Acid ChloridesChapter 21 - Carboxylic Acid DerivativesChapter 21.2F - Nomenclature Of Multifunctional CompoundsChapter 21.4A - Infrared SpectroscopyChapter 21.5C - Leaving Groups In Nucleophilic Acyl SubstitutionsChapter 21.6 - TransesterificationChapter 21.7B - Hydrolysis Of EstersChapter 21.7C - Hydrolysis Of AmidesChapter 21.7D - Hydrolysis Of NitrilesChapter 21.8A - Reduction To AlcoholsChapter 21.8C - Reduction To AminesChapter 21.9 - Reactions Of Acid Derivatives With Organometallic ReagentsChapter 21.10 - Summary Of The Chemistry Of Acid ChloridesChapter 21.11 - Summary Of The Chemistry Of AnhydridesChapter 21.12 - Summary Of The Chemistry Of EstersChapter 21.13 - Summary Of The Chemistry Of AmidesChapter 21.14 - Summary Of The Chemistry Of NitrilesChapter 21.16 - Esters And Amides Of Carbonic AcidChapter 22 - Condensations And Alpha Substitutions Of Carbonyl CompoundsChapter 22.2A - Keto-enol TautomerismChapter 22.4 - Formation And Alkylation Of EnaminesChapter 22.5A - Base-promoted Α-halogenationChapter 22.5B - The Haloform ReactionChapter 22.5C - Acid-catalyzed Alpha HalogenationChapter 22.6 - Alpha Bromination Of Acids: The Hvz ReactionChapter 22.7A - Base-catalyzed Aldon CondensationsChapter 22.7B - Acid-catalyzed Aldol CondensationsChapter 22.8 - Dehydration Of Aldol ProductsChapter 22.9 - Crossed Aldol CondensationsChapter 22.10 - Aldol CyclizationsChapter 22.11 - Planning Syntheses Using Aldol CondensationsChapter 22.12 - The Claisen Ester CondensationChapter 22.13 - The Dieckmann Condesnation: A Claisen CyclizationChapter 22.14 - Crossed Claisen CondensationChapter 22.15 - Syntheses Using Β-dicarbonyl CompoundsChapter 22.16 - The Malonic Ester SynthesisChapter 22.17 - The Acetoacetic Ester SynthesisChapter 22.18 - Conjugate Additions: The Michael ReactionChapter 22.19 - The Robinson AnnulationChapter 23 - Carbohydrates And Nucleic AcidsChapter 23.2 - Classification Of CarbohydratesChapter 23.3A - Classification Of MonosaccharidesChapter 23.3B - The D And L Configuration Of SugarsChapter 23.3C - EpimersChapter 23.4 - Cyclic Structures Of MonosaccharidesChapter 23.5 - Anomers Of Monosaccharides; MutarotationChapter 23.6 - Reactions Of Monosaccharides: ReductionChapter 23.7 - Oxidation Of Monosaccharides; Reducing SugarsChapter 23.8 - Nonreducing Sugars: Formation Of GlycosidesChapter 23.9 - Ether And Ester FormationChapter 23.10 - Chain Shortening: The Ruff DegradationChapter 23.11 - Chain Lengthening: The Kiliani-fischer SynthesisChapter 23.12A - The 1,4' Linkage: Cellobiose, Maltose, And LactoseChapter 23.12B - The 1,6' Linkage: GentiobioseChapter 23.12C - Linkage Of Two Anomeric Carbons: SucroseChapter 23.13A - CelluloseChapter 23.15 - Ribonucleosides And RibonucleotidesChapter 23.16C - Base PairingChapter 24 - Amino Acids, Peptides, And ProteinsChapter 24.2A - The Standard Amino Acids Of ProteinsChapter 24.2B - Essential Amino AcidsChapter 24.4 - Isoelectric Points And ElectrophoresisChapter 24.5A - Reductive AminationChapter 24.5B - Amination Of An Α-halo AcidChapter 24.5C - The Strecker SynthesisChapter 24.6 - Resolution Of Amino AcidsChapter 24.7A - Esterification Of The Carboxyl GroupChapter 24.7B - Acylation Of The Amino Group: Formation Of AmidesChapter 24.7C - Reaction With NinhydrinChapter 24.8B - Peptide NomenclatureChapter 24.9C - Sequencing From The N-terminus: The Edman DegradationChapter 24.9E - Breaking The Peptide Into Shorter Chains: Partial HydrolysisChapter 24.10A - The Individual ReactionsChapter 24.10B - An Example Of Solid-phase Peptide SynthesisChapter 25 - LipidsChapter 25.3 - TriglyceridesChapter 25.3A - Hydrogenation Of Triglycerides; Trans FatsChapter 25.3B - Transesterification Of Fats And Oils To BiodieselChapter 25.4 - Saponification Of Fats And Oils: Soaps And DetergentsChapter 25.5 - PhospholipidsChapter 25.6 - SteroidsChapter 25.8A - Characteristics And Nomenclature Of TerpenesChapter 25.8B - Classification Of TerpenesChapter 26 - Synthetic PolymersChapter 26.2A - Free-radical PolymerizationChapter 26.2B - Cationic PolymerizationChapter 26.2C - Anionic PolymerizationChapter 26.3 - Stereochemistry Of PolymersChapter 26.5 - Natural And Synthetic RubbersChapter 26.6 - Copolymers Of Two Or More MonomersChapter 26.7A - Polyamides: NylonChapter 26.7B - PolyestersChapter 26.7C - PolycarbonatesChapter 26.7D - Polyurethanes

Book Details

A Student-Centered Approach to Learning and Studying Organic Chemistry. Wade & Simek's Ninth edition of Organic Chemistry presents key principles of organic chemistry in the context of fundamental reasoning and problem solving. Authored to complement how students use a textbook today, new Problem Solving Strategies, Partially Solved Problems, Visual Reaction Guides and Reaction Starbursts encourage students to use the text before class as a primary introduction to organic chemistry as well as a comprehensive study tool for working problems and/or preparing for exams. With unparalleled and highly refined pedagogy, this Ninth edition gives students a contemporary overview of organic principles and the tools for organizing and understanding reaction mechanisms and synthetic organic chemistry.

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Organic Chemistry and CW+ GradeTracker Access Card Package
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