Organic Chemistry - 8th Edition - by William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote - ISBN 9781305580350
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Organic Chemistry
8th Edition
William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher: Cengage Learning
ISBN: 9781305580350

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Chapter 2.2 - Constitutional Isomerism In AlkanesChapter 2.3 - Nomenclature Of Alkanes And The Iupac SystemChapter 2.4 - CycloalkanesChapter 2.5 - Conformations Of Alkanes And CycloalkanesChapter 2.6 - Cis,trans Isomerism In Cycloalkanes And BicycloalkanesChapter 2.7 - Physical Properties Of Alkanes And CycloalkanesChapter 3 - Stereoisomerism And ChiralityChapter 3.2 - StereoisomerismChapter 3.3 - Naming Chiral Centers—the R,s SystemChapter 3.4 - Acyclic Molecules With Two Or More StereocentersChapter 3.5 - Cyclic Molecules With Two Or More Chiral CentersChapter 3.7 - Optical Activity—how Chirality Is Detected In The LaboratoryChapter 3.8 - The Significance Of Chirality In The Biological WorldChapter 4 - Acids And BasesChapter 4.2 - Br?nsted-lowry Acids And BasesChapter 4.3 - Acid Dissociation Constants, Pka, And The Relative Strengths Of Acids And BasesChapter 4.4 - The Position Of Equilibrium In Acid-base ReactionsChapter 4.5 - Thermochemistry And Mechanisms Of Acid-base ReactionsChapter 4.6 - Molecular Structure And AcidityChapter 4.7 - Lewis Acids And BasesChapter 5 - Alkenes: Bonding, Nomenclature, And PropertiesChapter 5.1 - Structure Of AlkenesChapter 5.2 - Nomenclature Of AlkenesChapter 6 - Reactions Of AlkenesChapter 6.2 - Organic Reactions Involving Reactive IntermediatesChapter 6.3 - Electrophilic AdditionsChapter 6.4 - Hydroboration-oxidationChapter 6.5 - OxidationChapter 7 - AlkynesChapter 7.2 - Nomenclature Of AlkynesChapter 7.5 - Preparation Of AlkynesChapter 7.7 - Hydration Of Alkynes To Aldehydes And KetonesChapter 7.9 - Organic SynthesisChapter 8 - Haloalkanes, Halogenation, And Radical ReactionsChapter 8.2 - NomenclatureChapter 8.4 - Preparation Of Haloalkanes By Halogenation Of AlkanesChapter 8.5 - Mechanism Of Halogenation Of AlkanesChapter 8.6 - Allylic HalogenationChapter 8.7 - Radical AutoxidationChapter 8.8 - Radical Addition Of Hbr To AlkenesChapter 9 - Nucleophilic Substitution And Β-eliminationChapter 9.1 - Nucleophilic Substitution In HaloalkanesChapter 9.3 - Experimental Evidence For Sn1 And Sn2 MechanismsChapter 9.4 - Analysis Of Several Nucleophilic Substitution ReactionsChapter 9.5 - Β-eliminationChapter 9.7 - Experimental Evidence For E1 And E2 MechanismsChapter 9.9 - Analysis Of Several Competitions Between Substitutions And EliminationsChapter 9.10 - Neighboring Group ParticipationChapter 10 - AlcoholsChapter 10.1 - Structure And Nomenclature Of AlcoholsChapter 10.2 - Physical Properties Of AlcoholsChapter 10.4 - Reaction Of Alcohols With Active MetalsChapter 10.5 - Conversion Of Alcohols To Haloalkanes And SulfonatesChapter 10.6 - Acid-catalyzed Dehydration Of AlcoholsChapter 10.7 - The Pinacol RearrangementChapter 10.8 - Oxidation Of AlcoholsChapter 10.9 - ThiolsChapter 11 - Ethers, Epoxides, And SulfidesChapter 11.2 - Nomenclature Of EthersChapter 11.3 - Physical Properties Of EthersChapter 11.4 - Preparation Of EthersChapter 11.5 - Reactions Of EthersChapter 11.6 - Silyl Ethers As Protecting GroupsChapter 11.8 - Synthesis Of EpoxidesChapter 11.9 - Reactions Of EpoxidesChapter 12 - Infrared SpectroscopyChapter 12.3 - Infrared SpectroscopyChapter 13 - Nuclear Magnetic Resonance SpectroscopyChapter 13.2 - Orientation Of Nuclear Spins In An Applied Magnetic FieldChapter 13.5 - Equivalent HydrogensChapter 13.6 - Signal AreasChapter 13.7 - Chemical ShiftChapter 13.8 - Signal Splitting And The (n + 1) RuleChapter 13.10 - Stereochemistry And TopicityChapter 13.11 - 13c-nmrChapter 14 - Mass SpectrometryChapter 14.2 - Features Of A Mass SpectrumChapter 14.3 - Interpreting Mass SpectraChapter 15 - An Introduction To Organometallic CompoundsChapter 15.1 - Organomagnesium And Organolithium CompoundsChapter 15.2 - Lithium Diorganocopper (gilman) ReagentsChapter 16 - Aldehydes And KetonesChapter 16.1 - Structure And BondingChapter 16.5 - Addition Of Carbon NucleophilesChapter 16.6 - The Wittig ReactionChapter 16.7 - Addition Of Oxygen NucleophilesChapter 16.8 - Addition Of Nitrogen NucleophilesChapter 16.9 - Keto-enol TautomerismChapter 16.10 - OxidationChapter 16.11 - ReductionChapter 17 - Carboxylic AcidsChapter 17.2 - NomenclatureChapter 17.4 - AcidityChapter 17.7 - EsterificationChapter 17.8 - Conversion To Acid ChloridesChapter 17.9 - DecarboxylationChapter 18 - Functional Derivatives Of Carboxylic AcidsChapter 18.1 - Structure And NomenclatureChapter 18.2 - Acidity Of Amides, Imides, And SulfonamidesChapter 18.4 - Reaction With Water: HydrolysisChapter 18.5 - Reaction With AlcoholsChapter 18.6 - Reactions With Ammonia And AminesChapter 18.8 - Interconversion Of Functional DerivativesChapter 18.9 - Reactions With Organometallic CompoundsChapter 18.10 - ReductionChapter 19 - Enolate Anions And EnaminesChapter 19.2 - Aldol ReactionChapter 19.3 - Claisen And Dieckmann CondensationsChapter 19.5 - EnaminesChapter 19.6 - Acetoacetic Ester SynthesisChapter 19.7 - Malonic Ester SynthesisChapter 19.8 - Conjugate Addition To A,b-unsaturated Carbonyl CompoundsChapter 19.9 - Crossed Enolate Reactions Using LdaChapter 20 - Dienes, Conjugated Systems, And Pericyclic ReactionsChapter 20.1 - Stability Of Conjugated DienesChapter 20.2 - Electrophilic Addition To Conjugated DienesChapter 20.3 - Uv-visible SpectroscopyChapter 20.4 - Pericyclic Reaction TheoryChapter 20.5 - The Diels-alder ReactionChapter 20.6 - Sigmatropic ShiftsChapter 21 - Benzene And The Concept Of AromaticityChapter 21.2 - The Concept Of AromaticityChapter 21.3 - NomenclatureChapter 21.4 - PhenolsChapter 21.5 - Reactions At A Benzylic PositionChapter 22 - Reactions Of Benzene And Its DerivativesChapter 22.1 - Electrophilic Aromatic SubstitutionChapter 22.2 - Disubstitution And PolysubstitutionChapter 22.3 - Nucleophilic Aromatic SubstitutionChapter 23 - AminesChapter 23.1 - Structure And ClassificationChapter 23.2 - NomenclatureChapter 23.5 - BasicityChapter 23.6 - Reactions With AcidsChapter 23.7 - PreparationChapter 23.8 - Reaction With Nitrous AcidChapter 23.9 - Hofmann EliminationChapter 23.10 - Cope EliminationChapter 24 - Catalytic Carbon-carbon Bond FormationChapter 24.3 - The Heck ReactionChapter 24.4 - Catalytic Allylic AlkylationChapter 24.5 - Palladium-catalyzed Cross-coupling ReactionsChapter 24.6 - Alkene MetathesisChapter 25 - CarbohydratesChapter 25.1 - MonosaccharidesChapter 25.2 - The Cyclic Structure Of MonosaccharidesChapter 25.3 - Reactions Of MonosaccharidesChapter 25.4 - Disaccharides And OligosaccharidesChapter 26 - LipidsChapter 26.1 - TriglyceridesChapter 26.6 - Fat-soluble VitaminsChapter 27 - Amino Acids And ProteinsChapter 27.1 - Amino AcidsChapter 27.2 - Acid-base Properties Of Amino AcidsChapter 27.3 - Polypeptides And ProteinsChapter 27.4 - Primary Structure Of Polypeptides And ProteinsChapter 27.6 - Three-dimensional Shapes Of Polypeptides And ProteinsChapter 28 - Nucleic AcidsChapter 28.1 - Nucleosides And NucleotidesChapter 28.2 - The Structure Of DnaChapter 28.3 - Ribonucleic AcidsChapter 28.4 - The Genetic CodeChapter 28.5 - Sequencing Nucleic AcidsChapter 29 - Organic Polymer ChemistryChapter 29.2 - Polymer Notation And NomenclatureChapter 29.5 - Step-growth PolymerizationsChapter 29.6 - Chain-growth Polymerizations

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Which are secondary alcohols?Write names for these compounds. Where possible, write both IUPAC names and common names.Following are infrared spectra of methylenecyclopentane and 2,3-dimethyl-2-butene. Assign each...Calculate the index of hydrogen deficiency of these compounds. (a) Aspirin, C9H8O4 (b) Ascorbic acid...Draw acceptable Lewis structures for the molecular ion (radical cation) formed from the following...Complete these reactions involving lithium diorganocopper (Gilman) reagents. (a) (b) (c) (d)Name each compound, showing stereochemistry where relevant.Write the IUPAC name of each compound, showing stereochemistry where relevant.Draw a structural formula for each compound. (a) Dimethyl carbonate (b) Benzonitrile (c) Isopropyl...Draw a structural formula for the product of the aldol reaction of each compound and for the...If an electron is added to 1,3-butadiene, into which molecular orbital does it go? If an electron is...Name the following compounds and ions.Pyridine undergoes electrophilic aromatic substitution preferentially at the 3 position as...Draw a structural formula for each amine and amine derivative. (a) N,N-Dimethylaniline (b)...As has been demonstrated in the text, when the starting alkene has CH2 as its terminal group, the...Explain the meaning of the designations D and L used to specify the configuration of...Define the term hydrophobic.What amino acid does each abbreviation stand for? (a) Phe (b) Ser (c) Asp (d) Gln (e) His (f) Gly...A pioneer in designing and synthesizing antimetabolites that could destroy cancer cells was George...Name the following polymers.

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