Package: Loose Leaf For Organic Chemistry With Connect Access Card (1 Semester) - 6th Edition - by Janice Gorzynski Smith Dr. - ISBN 9781260699098

Package: Loose Leaf For Organic Chemist...
6th Edition
Janice Gorzynski Smith Dr.
Publisher: McGraw-Hill Education
ISBN: 9781260699098

Solutions for Package: Loose Leaf For Organic Chemistry With Connect Access Card (1 Semester)

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Chapter 2.2 - Reactions Of Brønsted–lowry Acids And BasesChapter 2.3 - Acid Strength And PkaChapter 2.4 - Predicting The Outcome Of Acid–base ReactionsChapter 2.5 - Factors That Determine Acid StrengthChapter 2.6 - Common Acids And BasesChapter 2.7 - AspirinChapter 2.8 - Lewis Acids And BasesChapter 3 - Introduction To Organic Molecules And Functional GroupsChapter 3.1 - Functional GroupsChapter 3.2 - An Overview Of Functional GroupsChapter 3.4 - Physical PropertiesChapter 3.5 - Application: VitaminsChapter 4 - AlkanesChapter 4.1 - Alkanes—an IntroductionChapter 4.2 - CycloalkanesChapter 4.4 - Naming AlkanesChapter 4.5 - Naming CycloalkanesChapter 4.8 - Properties Of AlkanesChapter 4.9 - Conformations Of Acyclic Alkanes—ethaneChapter 4.10 - Conformations Of ButaneChapter 4.12 - CyclohexaneChapter 4.13 - Substituted CycloalkanesChapter 4.14 - Oxidation Of AlkanesChapter 4.15 - Lipids—partChapter 5 - StereochemistryChapter 5.1 - Starch And CelluloseChapter 5.2 - The Two Major Classes Of IsomersChapter 5.3 - Looking Glass Chemistry—chiral And Achiral MoleculesChapter 5.6 - Labeling Stereogenic Centers With R Or SChapter 5.7 - DisastereomersChapter 5.8 - Meso CompoundsChapter 5.9 - R And S Assignments In Compounds With Two Or More Stereogenic CentersChapter 5.10 - Disubstituted CycloalkanesChapter 5.11 - Isomers—a SummaryChapter 5.12 - Physical Properties Of StereoisomersChapter 6 - Understanding Organic ReactionsChapter 6.2 - Kinds Of Organic ReactionsChapter 6.3 - Bond Breaking And Bond MakingChapter 6.4 - Bond Dissociation EnergyChapter 6.5 - ThermodynamicsChapter 6.6 - Enthalpy And EntropyChapter 6.7 - Energy DiagramsChapter 6.8 - Energy Diagram For A Two-step Reaction MechanismChapter 6.9 - KineticsChapter 6.10 - CatalystsChapter 7 - Alkyl Halides And Nucleophilic SubstitutionChapter 7.1 - Introduction To Alkyl HalidesChapter 7.2 - NomenclatureChapter 7.3 - Properties Of Alkyl HalidesChapter 7.4 - Interesting Alkyl HalidesChapter 7.6 - General Features Of Nucleophilic SubstitutionChapter 7.7 - The Leaving GroupChapter 7.8 - The NucleophileChapter 7.11 - The Sn2 MechanismChapter 7.12 - The Sn1 MechanismChapter 7.13 - Carbocation StabilityChapter 7.15 - When Is The Mechanism Sn1 Or Sn2?Chapter 8 - Alkyl Halides And Elimination ReactionsChapter 8.1 - General Features Of EliminationChapter 8.2 - Alkenes—the Products Of Elimination ReactionsChapter 8.4 - The E2 MechanismChapter 8.5 - The Zaitsev RuleChapter 8.6 - The E1 MechanismChapter 9 - Alcohols, Ethers, And Related CompoundsChapter 9.1 - IntroductionChapter 9.3 - NomenclatureChapter 9.6 - Preparation Of Alcohols, Ethers, And EpoxidesChapter 9.8 - Dehydration Of Alcohols To AlkenesChapter 9.11 - Conversion Of Alcohols To Alkyl Halides With HxChapter 9.12 - Conversion Of Alcohols To Alkyl Halides With Socl2 And Pbr3Chapter 9.13 - Tosylate—another Good Leaving GroupChapter 9.14 - Reaction Of Ethers With Strong AcidChapter 9.15 - Thiols And SulfidesChapter 9.16 - Reactions Of EpoxidesChapter 10 - Alkenes And Addition ReactionsChapter 10.1 - IntroductionChapter 10.2 - Calculating Degrees Of UnsaturationChapter 10.3 - NomenclatureChapter 10.6 - Lipids—partChapter 10.7 - Preparation Of AlkenesChapter 10.9 - Hydrohalogenation—electrophilic Addition Of HxChapter 10.10 - Markovnikov’s RuleChapter 10.11 - Stereochemistry Of Electrophilic Addition Of HxChapter 10.12 - Hydration—electrophilic Addition Of WaterChapter 10.13 - Halogenation—addition Of HalogenChapter 10.14 - Stereochemistry Of HalogenationChapter 10.15 - Halohydrin FormationChapter 10.16 - Hydroboration–oxidationChapter 10.17 - Keeping Track Of ReactionsChapter 10.18 - Alkenes In Organic SynthesisChapter 11 - Alkynes And SynthesisChapter 11.1 - IntroductionChapter 11.2 - NomenclatureChapter 11.3 - Properties Of AlkynesChapter 11.5 - Preparation Of AlkynesChapter 11.6 - Introduction To Alkyne ReactionsChapter 11.7 - Addition Of Hydrogen HalidesChapter 11.8 - Addition Of HalogenChapter 11.9 - Addition Of WaterChapter 11.10 - Hydroboration–oxidationChapter 11.11 - Reaction Of Acetylide AnionsChapter 12 - Oxidation And ReductionChapter 12.1 - IntroductionChapter 12.3 - Reduction Of AlkenesChapter 12.4 - Application: Hydrogenation Of OilsChapter 12.5 - Reduction Of AlkynesChapter 12.6 - The Reduction Of Polar C–x Σ BondsChapter 12.8 - EpoxidationChapter 12.9 - DihydroxylationChapter 12.10 - Oxidative Cleavage Of AlkenesChapter 12.11 - Oxidative Cleavage Of AlkynesChapter 12.12 - Oxidation Of AlcoholsChapter 12.13 - Green ChemistryChapter 12A - Mass SpectrometryChapter 12A.1 - Mass Spectrometry And The Molecular IonChapter 12A.2 - Alkyl Halides And The M + 2 PeakChapter 12A.3 - FragmentationChapter 12C - Nuclear Magnetic Resonance SpectroscopyChapter 12C.1 - An Introduction To Nmr SpectroscopyChapter 12C.2 - 1h Nmr: Number Of SignalsChapter 12C.3 - 1h Nmr: Position Of SignalsChapter 12C.4 - The Chemical Shifts Of Protons On Sp2 And Sp Hybridized CarbonsChapter 12C.5 - 1h Nmr: Intensity Of SignalsChapter 12C.6 - 1h Nmr: Spin–spin SplittingChapter 12C.7 - More-complex Examples Of SplittingChapter 12C.8 - Spin–spin Splitting In AlkenesChapter 12C.9 - Other Facts About 1h Nmr SpectroscopyChapter 12C.10 - Using 1h Nmr To Identify An UnknownChapter 13 - Radical ReactionsChapter 13.1 - IntroductionChapter 13.2 - General Features Of Radical ReactionsChapter 13.3 - Halogenation Of AlkanesChapter 13.4 - The Mechanism Of HalogenationChapter 13.5 - Chlorination Of Other AlkanesChapter 13.6 - Chlorination Versus BrominationChapter 13.7 - Halogenation As A Tool In Organic SynthesisChapter 13.8 - The Stereochemistry Of Halogenation ReactionsChapter 14 - Conjugation, Resonance, And DienesChapter 14.1 - ConjugationChapter 14.2 - Resonance And Allylic CarbocationsChapter 14.3 - Common Examples Of ResonanceChapter 14.4 - The Resonance HybridChapter 14.8 - The Carbon–carbon Σ Bond Length In Buta-1,3-dieneChapter 14.9 - Stability Of Conjugated DienesChapter 14.10 - Electrophilic Addition: 1,2- Versus 1,4-additionChapter 14.11 - Kinetic Versus Thermodynamic ProductsChapter 14.12 - The Diels–alder ReactionChapter 15 - Benzene And Aromatic CompoundsChapter 15.2 - The Structure Of BenzeneChapter 15.3 - Nomenclature Of Benzene DerivativesChapter 15.6 - Benzene’s Unusual StabilityChapter 15.8 - Examples Of Aromatic CompoundsChapter 16 - Reactions Of Aromatic CompoundsChapter 16.1 - Electrophilic Aromatic SubstitutionChapter 16.2 - The General MechanismChapter 16.3 - HalogenationChapter 16.4 - Nitration And SulfonationChapter 16.5 - Friedel–crafts Alkylation And Friedel–crafts AcylationChapter 16.6 - Substituted BenzenesChapter 16.7 - Electrophilic Aromatic Substitution Of Substituted BenzenesChapter 16.9 - Orientation Effects In Substituted BenzenesChapter 16.10 - Limitations On Electrophilic Substitution Reactions With Substituted BenzenesChapter 16.11 - Disubstituted BenzenesChapter 16.12 - Synthesis Of Benzene DerivativesChapter 16.13 - Nucleophilic Aromatic SubstitutionChapter 17 - Introduction To Carbonyl Chemistry; Organometallic Reagents; Oxidation And ReductionChapter 17.1 - IntroductionChapter 17.2 - General Reactions Of Carbonyl CompoundsChapter 17.4 - Reduction Of Aldehydes And KetonesChapter 17.5 - The Stereochemistry Of Carbonyl ReductionChapter 17.7 - Reduction Of Carboxylic Acids And Their DerivativesChapter 17.8 - Oxidation Of AldehydesChapter 17.9 - Organometallic ReagentsChapter 17.10 - Reaction Of Organometallic Reagents With Aldehydes And KetonesChapter 17.11 - Retrosynthetic Analysis Of Grignard ProductsChapter 17.12 - Protecting GroupsChapter 17.13 - Reaction Of Organometallic Reagents With Carboxylic Acid DerivativesChapter 17.14 - Reaction Of Organometallic Reagents With Other CompoundsChapter 18 - Aldehydes And Ketones—nucleophilic AdditionChapter 18.1 - IntroductionChapter 18.2 - NomenclatureChapter 18.5 - Preparation Of Aldehydes And KetonesChapter 18.9 - The Wittig ReactionChapter 18.10 - Addition Of 1° AminesChapter 18.11 - Addition Of 2° AminesChapter 18.12 - Addition Of H2o—hydrationChapter 18.13 - Addition Of Alcohols—acetal FormationChapter 20 - Carboxylic Acids And Their Derivatives—nucleophilic Acyl SubstitutionChapter 20.1 - IntroductionChapter 20.2 - Structure And BondingChapter 20.3 - NomenclatureChapter 20.4 - Physical And Spectroscopic PropertiesChapter 20.7 - Reactions Of Acid ChloridesChapter 20.8 - Reactions Of AnhydridesChapter 20.9 - Reactions Of Carboxylic AcidsChapter 20.10 - Reactions Of EstersChapter 21 - Substitution Reactions Of Carbonyl Compounds At The α CarbonChapter 21.2 - EnolsChapter 21.3 - EnolatesChapter 21.4 - Enolates Of Unsymmmetrical Carbonyl CompoundsChapter 21.5 - Racemization At The α CarbonChapter 21.7 - Halogenation At The α CarbonChapter 21.8 - Direct Enolate AlkylationChapter 21.9 - Malonic Ester SynthesisChapter 21.10 - Acetoacetic Ester SynthesisChapter 22 - Carbonyl Condensation ReactionsChapter 22.1 - The Aldol ReactionChapter 22.2 - Crossed Aldol ReactionsChapter 22.4 - Intramolecular Aldol ReactionsChapter 22.5 - The Claisen ReactionChapter 22.6 - The Crossed Claisen And Related ReactionsChapter 22.7 - The Dieckmann ReactionChapter 22.8 - The Michael ReactionChapter 23 - AminesChapter 23.2 - Structure And BondingChapter 23.3 - NomenclatureChapter 23.4 - Physical And Spectroscopic PropertiesChapter 23.6 - Preparation Of AminesChapter 23.8 - Amines As BasesChapter 23.9 - Relative Basicity Of Amines And Other CompoundsChapter 23.10 - Amines As NucleophilesChapter 23.11 - Hofmann EliminationChapter 23.12 - Reactions Of Amines With Nitrous AcidChapter 23.13 - Substitution Reactions Of Aryl Diazonium SaltsChapter 24 - Carbon–carbon Bond-forming Reactions In Organic SynthesisChapter 24.1 - Coupling Reactions Of Organocuprate ReagentsChapter 24.2 - Suzuki ReactionChapter 24.4 - Carbenes And Cyclopropane SynthesisChapter 24.5 - Simmons–smith ReactionChapter 24.6 - MetathesisChapter 25 - Pericyclic ReactionsChapter 25.1 - Types Of Pericyclic ReactionsChapter 25.2 - Molecular OrbitalsChapter 25.3 - Electrocyclic ReactionsChapter 25.4 - Cycloaddition ReactionsChapter 25.5 - Sigmatropic RearrangementsChapter 25.6 - Summary Of Rules For Pericyclic ReactionsChapter 26 - CarbohydratesChapter 26.2 - MonosaccharidesChapter 26.3 - The Family Of D-aldosesChapter 26.4 - The Family Of D-ketosesChapter 26.6 - The Cyclic Forms Of MonosaccharidesChapter 26.7 - GlycosidesChapter 26.8 - Reactions Of Monosaccharides At The Oh GroupsChapter 26.9 - Reactions At The Carbonyl Group—oxidation And ReductionChapter 26.10 - Reactions At The Carbonyl Group—adding Or Removing One Carbon AtomChapter 26.11 - DisaccharidesChapter 26.12 - PolysaccharidesChapter 26.13 - Other Important Sugars And Their DerivativesChapter 27 - Amino Acids And ProteinsChapter 27.1 - Amino AcidsChapter 27.2 - Synthesis Of Amino AcidsChapter 27.3 - Separation Of Amino AcidsChapter 27.4 - Enantioselective Synthesis Of Amino AcidsChapter 27.5 - PeptidesChapter 28 - Synthetic PolymersChapter 28.1 - IntroductionChapter 28.2 - Chain-growth Polymers—addition PolymersChapter 28.3 - Anionic Polymerization Of EpoxidesChapter 28.5 - Natural And Synthetic RubbersChapter 28.6 - Step-growth Polymers—condensation PolymersChapter 28.7 - Polymer Structure And PropertiesChapter 28.8 - Green Polymer SynthesisChapter 28.9 - Polymer Recycling And DisposalChapter 29 - Lipids 1292 (available Online)Chapter 29.2 - WaxesChapter 29.3 - TriacylglycerolsChapter 29.7 - TerpenesChapter 29.8 - Steroids

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