ORGANIC CHEM.-PRINT COMP.(LL)W/2 ACCESS - 3rd Edition - by Klein - ISBN 9781119340607

ORGANIC CHEM.-PRINT COMP.(LL)W/2 ACCESS
3rd Edition
Klein
Publisher: WILEY
ISBN: 9781119340607

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Chapter 2 - Molecular RepresentationsChapter 2.1 - Molecular RepresentationsChapter 2.2 - Bond-line StructuresChapter 2.3 - Identifying Functional GroupsChapter 2.5 - Identifying Lone PairsChapter 2.8 - Curved ArrowsChapter 2.9 - Formal Charges In Resonance StructuresChapter 2.10 - Drawing Resonance Structures Via Pattern RecognitionChapter 2.11 - Assessing Relative Importance Of Resonance StructuresChapter 2.12 - The Resonance HybridChapter 2.13 - Delocalized And Localized Lone PairsChapter 3 - Acids And BasesChapter 3.2 - Flow Of Electron Density: Curved Arrow NotationChapter 3.3 - Bronsted-lowry Acidity: A Quantitative PerspectiveChapter 3.4 - Bronsted-lowry Acidity: Qualitative PerspectiveChapter 3.5 - Position Of Equilibrium And Choice Of ReagentsChapter 3.7 - Solvating EffectsChapter 3.9 - Lewis Acids And BasesChapter 4 - Alkanes And CycloalkanesChapter 4.2 - Nomenclature Of AlkanesChapter 4.3 - Constitutional Isomers Of AlkanesChapter 4.6 - Drawing Newman ProjectionsChapter 4.7 - Conformational Analysis Of Ethane And PropaneChapter 4.8 - Conformational Analysis Of ButaneChapter 4.11 - Drawing Chair ConformationsChapter 4.12 - Monusubstituted CyclohexaneChapter 4.13 - Disubstituted CyclohexaneChapter 4.14 - Cis-trans StereoisomerismChapter 5 - StereoisomerismChapter 5.1 - Overview Of IsomerismChapter 5.2 - Introduction To StereoisomerismChapter 5.3 - Designating Configuration Using The Cahn-ingold-prelog SystemChapter 5.4 - Optical ActivityChapter 5.5 - Stereoisomeric Relationships: Enantiomers And DiastereomersChapter 5.6 - Symmetry And ChiralityChapter 5.7 - Fischer ProjectionsChapter 5.9 - Chiral Compounds That Lack A Chiral CenterChapter 5.11 - E And Z Designations For Diastereomeric AlkenesChapter 6 - Chemical Reactivity And MechanismsChapter 6.1 - EnthalpyChapter 6.2 - EntropyChapter 6.3 - Gibbs Free EnergyChapter 6.4 - EquilibriaChapter 6.6 - Reading Energy DiagramsChapter 6.7 - Nucleophiles And ElectrophilesChapter 6.8 - Mechanisms And Arrow PushingChapter 6.9 - Combining The Patterns Of Arrow PushingChapter 6.10 - Drawing Curved ArrowsChapter 6.11 - Carbocation RearrangementsChapter 7 - Alkyl Halides: Nucleophilic Substitution And Elimination ReactionsChapter 7.2 - Nomenclature And Uses Of Alkyl HalidesChapter 7.3 - Sn2 ReactionsChapter 7.4 - Nucleophilic Strength And Solvent Effects In Sn2 ReactionsChapter 7.5 - Sn2 Reactions In Biological Systems-methylationChapter 7.6 - Introduction To E2 ReactionsChapter 7.7 - Nomenclature And Stability Of AlkenesChapter 7.8 - Regiochemical And Stereochemical Outcome For E2 ReactionsChapter 7.9 - Unimolecular Reactions: (sn1 And E1)Chapter 7.10 - Kinetic Isotope Effects In Elimination ReactionsChapter 7.11 - Predicting Products: Substitution Vs. EliminationChapter 7.12 - Substitution And Elimination Reactions With Other SubstratesChapter 7.13 - Synthesis StrategiesChapter 8 - Addition Reactions Of AlkenesChapter 8.4 - HydrohalogenationChapter 8.5 - Acid-catalyzed HydrationChapter 8.6 - Oxymercuration-demercurationChapter 8.7 - Hydroboration-oxidationChapter 8.8 - Catalytic HydrogenationChapter 8.9 - Halogenation And Halohydrin FormationChapter 8.10 - Anti DihydroxylationChapter 8.11 - Syn DihydroxylationChapter 8.12 - Oxidative OeavageChapter 8.13 - Predicting Products Of An Addition ReactionChapter 8.14 - Synthesis StrategiesChapter 9 - AlkynesChapter 9.2 - Nomenclature Of AlkynesChapter 9.3 - Acidity Of Acetylene And Terminal AlkynesChapter 9.4 - Preparation Of AlkynesChapter 9.5 - Reduction Of AlkynesChapter 9.6 - Hydrohalogenation Of AlkynesChapter 9.7 - Hydration Of AlkynesChapter 9.9 - Ozonolysis Of AlkynesChapter 9.10 - Alkylation Of Terminal AlkynesChapter 9.11 - Synthesis StrategiesChapter 10 - Radical ReactionsChapter 10.1 - RadicalsChapter 10.2 - Common Patterns In Radical MechanismsChapter 10.3 - Chlorination Of MethaneChapter 10.5 - Selectivity Of HalogenationChapter 10.6 - Stereochemistry Of HalogenationChapter 10.7 - Allylic BrominationChapter 10.8 - Atmospheric Chemistry And The Ozone LayerChapter 10.9 - Autooxidation And AntioxidantsChapter 10.10 - Radical Addition Of Hbr: Anti-markovnikov AdditionChapter 11 - SynthesisChapter 11.1 - One-step SynthesesChapter 11.2 - Functional Group TransformationsChapter 11.3 - Reactions That Change The Carbon SkeletonChapter 11.4 - How To Approach A Synthesis ProblemChapter 11.5 - Retrosynthetic AnalysisChapter 12 - Alcohols And PhenolsChapter 12.1 - Structure And Properties Of AlcoholsChapter 12.2 - Acidity Of Alcohols And PhenolsChapter 12.3 - Preparation Of Alcohols Via Substitution Or AdditionChapter 12.4 - Preparation Of Alcohols Via ReductionChapter 12.6 - Preparation Of Alcohols Via Grignard ReagentsChapter 12.7 - Protection Of AlcoholsChapter 12.9 - Reactions Of Alcohols: Substitution And EliminationChapter 12.10 - Reactions Of Alcohols: OxidationChapter 12.13 - Synthesis StrategiesChapter 13 - Ethers And Epoxides; Thiols And SulfidesChapter 13.2 - Nomenclature Of EthersChapter 13.4 - Crown EthersChapter 13.5 - Preparation Of EthersChapter 13.6 - Reactions Of EthersChapter 13.7 - Nomenclature Of EpoxidesChapter 13.8 - Preparation Of EpoxidesChapter 13.9 - Enantioselective EpoxidationChapter 13.10 - Ring-opening Reactions Of EpoxidesChapter 13.11 - Thiols And SulfidesChapter 13.12 - Synthesis Strategies Involving EpoxidesChapter 14 - Infrared Spectroscopy And Mass SpectrometryChapter 14.3 - Signal Characteristics: WavenumberChapter 14.4 - Signal Characteristics: IntensityChapter 14.5 - Signal Characteristics: ShapeChapter 14.6 - Analyzing An Ir SpectrumChapter 14.7 - Using Ir Spectroscopy To Distinguish Between Two CompoundsChapter 14.9 - Analyzing The (m)+" PeakChapter 14.10 - Analyzing The (m+1)+" PeakChapter 14.11 - Analyzing The (m+2)+"· PeakChapter 14.12 - Analyzing The FragmentsChapter 14.13 - High-resolution Mass SpectrometryChapter 14.16 - Hydrogen Deficiency Index: Degrees Of UnsaturationChapter 15 - Nuclear Magnetic Resonance SpectroscopyChapter 15.4 - Number Of SignalsChapter 15.5 - Chemical ShiftChapter 15.6 - IntegrationChapter 15.7 - MultiplicityChapter 15.8 - Drawing The Expected 1h Nmr Spectrum Of A CompoundChapter 15.9 - Using 1h Nmr Spectroscopy To Distinguish Between CompoundsChapter 15.10 - Analyzing A1h Nmr SpectrumChapter 15.12 - Chemical Shifts In 13c Nmr SpectroscopyChapter 15.13 - Dept 13c Nmr SpectroscopyChapter 16 - Conjugated Pi Systems And Pericyclic ReactionsChapter 16.1 - Classes Of DienesChapter 16.2 - Conjugated DienesChapter 16.3 - Molecular Orbital TheoryChapter 16.4 - Electrophilic AdditionChapter 16.5 - Thermodynamic Control Vs. Kinetic ControlChapter 16.7 - Diels-alder ReactionsChapter 16.8 - Mo Description Of CycloadditionsChapter 16.9 - Electrocyclic ReactionsChapter 16.10 - Sigmatropic RearrangementsChapter 16.11 - Uv-vis SpectroscopyChapter 16.12 - ColorChapter 17 - Aromatic CompoundsChapter 17.2 - Nomenclature Of Benzene DerivativesChapter 17.4 - Stability Of BenzeneChapter 17.5 - Aromatic Compounds Other Than BenzeneChapter 17.6 - Reactions At The Benzylic PositionChapter 17.7 - Reduction Of Benzene And Its DerivativesChapter 17.8 - Spectroscopy Of Aromatic CompoundsChapter 18 - Aromatic Substitution ReactionsChapter 18.2 - HalogenationChapter 18.3 - SulfonationChapter 18.4 - NitrationChapter 18.5 - Friedel-crafts AlkylationChapter 18.6 - Friedel-crafts AcylationChapter 18.7 - Activating GroupsChapter 18.8 - Deactivating GroupsChapter 18.9 - Halogens: The ExceptionChapter 18.10 - Determining The Directing Effects Of A SubstituentChapter 18.11 - Multiple SubstituentsChapter 18.12 - Synthesis StrategiesChapter 18.13 - Nucleophilic Aromatic SubstitutionChapter 18.14 - Elimination-additionChapter 18.15 - Identifying The Mechanism Of An Aromatic Substitution ReactionChapter 19 - Aldehydes And KetonesChapter 19.2 - NomenclatureChapter 19.3 - Preparing Aldehydes And Ketones: A ReviewChapter 19.4 - Introduction To Nucleophilic Addition ReactionsChapter 19.5 - Oxygen NucleophilesChapter 19.6 - Nitrogen NucleophilesChapter 19.7 - Hydrolysis Of Acetals, Lmines, And EnaminesChapter 19.8 - Sulfur NucleophilesChapter 19.9 - Hydrogen NucleophilesChapter 19.10 - Carbon NucleophilesChapter 19.11 - Baeyer-villiger Oxidation Of Aldehydes And KetonesChapter 19.12 - Synthesis StrategiesChapter 19.13 - Spectroscopic Analysis Of Aldehydes And KetonesChapter 20 - Carboxylic Acids And Their DerivativesChapter 20.2 - Nomenclature Of Carboxylic AcidsChapter 20.3 - Structure And Properties Of Carboxylic AcidsChapter 20.4 - Preparation Of Carboxylic AcidsChapter 20.5 - Reactions Of Carboxylic AcidsChapter 20.6 - Introduction To Carboxylic Acid DerivativesChapter 20.7 - Reactivity Of Carboxylic Acid DerivativesChapter 20.8 - Preparation And Reactions Of Acid ChloridesChapter 20.9 - Preparation And Reactions Of Acid AnhydridesChapter 20.10 - Preparation Of EstersChapter 20.11 - Reactions Of EstersChapter 20.12 - Preparation And Reactions Of AmidesChapter 20.13 - Preparation And Reactions Of NitrilesChapter 20.14 - Synthesis StrategiesChapter 20.15 - Spectroscopy Of Carboxylic Acids And Their DerivativesChapter 21 - Alpha Carbon Chemistry: Enols And EnolatesChapter 21.1 - Introduction To Alpha Carbon Chemistry: Enols And EnolatesChapter 21.2 - Alpha Halogenation Of Enols And EnolatesChapter 21.3 - Aldol ReactionsChapter 21.4 - Claisen CondensationsChapter 21.5 - Alkylation Of The Alpha PositionChapter 21.6 - Conjugate Addition ReactionsChapter 21.7 - Synthesis StrategiesChapter 22 - AminesChapter 22.2 - Nomenclature Of AminesChapter 22.3 - Properties Of AminesChapter 22.4 - Preparation Of Amines: A ReviewChapter 22.5 - Preparation Of Amines Via Substitution ReactionsChapter 22.6 - Preparation Of Amines Via Reductive AminationChapter 22.7 - Synthesis StrategiesChapter 22.8 - Acylation Of AminesChapter 22.9 - Hofmann EliminationChapter 22.10 - Reactions Of Amines With Nitrous AcidChapter 22.11 - Reactions Of Aryl Diazonium IonsChapter 22.12 - Nitrogen HeterocyclesChapter 22.13 - Spectroscopy Of AminesChapter 23 - Introduction To Organometallic CompoundsChapter 23.1 - General Properties Of Organometallic CompoundsChapter 23.2 - Organolithium And Organomagnesium CompoundsChapter 23.3 - Lithium Dialkyl Cuprates (gilman Reagents)Chapter 23.4 - The Simmons-smith Reactions And CarbenoidsChapter 23.5 - Stille CouplingChapter 23.6 - Suzuki CouplingChapter 23.7 - Negishi CouplingChapter 23.8 - The Heck ReactionChapter 23.9 - Alkene MetathesisChapter 24 - CarbohydratesChapter 24.2 - Classifying MonosaccharidesChapter 24.4 - Configuration Of KetosesChapter 24.5 - Cyclic Structures Of MonosaccharidesChapter 24.6 - Reactions Of MonosaccharidesChapter 24.7 - DisaccharideChapter 25 - Amino Acids, Peptides, And ProteinsChapter 25.2 - Structure And Properties Of Amino AcidsChapter 25.3 - Amino Acid SynthesisChapter 25.4 - Structure Of PeptidesChapter 25.5 - Sequencing A PeptideChapter 25.6 - Peptide SynthesisChapter 25.7 - Protein StructureChapter 26 - LipidsChapter 26.2 - WaxesChapter 26.3 - TriglyceridesChapter 26.4 - Reactions OftriglyceridesChapter 26.5 - PhospholipidsChapter 26.6 - SteroidsChapter 26.7 - ProstaglandinsChapter 26.8 - TerpenesChapter 27 - Synthetic PolymersChapter 27.2 - Nomenclature Of Synthetic PolymersChapter 27.3 - CopolymersChapter 27.4 - Polymer Classification By Reaction TypeChapter 27.5 - Polymer Classification By Mode Of AssemblyChapter 27.6 - Polymer Classification By StructureChapter 27.8 - Polymer Recycling

Book Details

Organic Chemistry with Student Solutions Manual & Study Guide, Enhanced eText, 3rd Edition is not merely a compilation of principles, but rather, it is a disciplined method of thought and analysis. Success in organic chemistry requires mastery in two core aspects: fundamental concepts and the skills needed to apply those concepts and solve problems. Readers must learn to become proficient at approaching new situations methodically, based on a repertoire of skills. These skills are vital for successful problem solving in organic chemistry. Existing textbooks provide extensive coverage of the principles but there is far less emphasis on the skills needed to actually solve problems.

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Explanation: The radical resonance structure of the given molecule The radical resonance structure...Explanation: Identify the reagents used in formation of products 1,2 and 3 from given substrate....Explanation: To find: IUPAC name of the compound The IUPAC name of the given organic compound is...Explanation: Predict the IUPAC nomenclature. The IUPAC name must contain all the information...The structure shows that the molecule contains one carbonyl group and one carbon-carbon double bond....Explanation: To predict: the structure for the given molecular formula. C5H10 Calculate HDI Value...Explanation To analyze the presence of prefix suffix and root name in the given IUPAC name and draw...Explanation: 4-ethylbenzoic acid From the structure of the compound it is clear that the parent...Explanation: Chlorination of benzene. Benzene reacts with Chlorine in an electrophilic substitution...Explanation (-C=O, -C-C-) in carbon chain or carbon skeleton, the substituents for naming the...Explanation: (a) To find: The increasing acidity order for the given set of compounds. Determine the...Explanation: Deprotonation of the highlighted hydrogen and resonance stabilization From the above...Explanation: The given compound, spermine contains totally four nitrogen atoms. Among them, two of...Analyzing both the given reactant clearly shows that the carbon atom present in C-Br bond in...Explanation: The OH group connected to C3 is pointing to the right side, so it is called as D-sugar....Explanation: Linear formula for L-valine The linear formula for L-valine is (CH3)2CHCH(NH2)CO2H ....Explanation: Structure of tripalmitolein The structure of tripalmitolein is drawn as above. In...Explanation: To draw and name the polymer when vinyl acetate undergoes polymerization Draw the...

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