MODIFIED MASTERING CHEMISTRY W/ ETEXT - 8th Edition - by Bruice - ISBN 9781323782507

MODIFIED MASTERING CHEMISTRY W/ ETEXT
8th Edition
Bruice
Publisher: PEARSON
ISBN: 9781323782507

Solutions for MODIFIED MASTERING CHEMISTRY W/ ETEXT

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Chapter 1.12 - The Bonds In WaterChapter 1.13 - The Bond In A Hydrogen HalideChapter 1.14 - Hybridization And Molecular GeometryChapter 1.15 - Summary: Hybridization, Bond Lengths, Bond Strengths, And Bond AnglesChapter 1.16 - Dipole Moments Of MoleculesChapter 2 - Acids And Bases: Central To Understanding Organic ChemistryChapter 2.1 - An Introduction To Acids And BasesChapter 2.2 - Pka And PhChapter 2.3 - Organic Acids And BasesChapter 2.4 - How To Predict The Outcome Of An Acid-base ReactionChapter 2.5 - How To Determine The Position Of EquilibriumChapter 2.6 - How The Structure Of An Acid Affects Its Pka ValueChapter 2.7 - How Substituents Affect The Strength Of An AcidChapter 2.8 - An Introduction To Delocalized ElectronsChapter 2.9 - A Summary Of The Factors That Determine Acid StrengthChapter 2.10 - How Ph Affects The Structure Of An Organic CompoundChapter 2.11 - Buffer SolutionsChapter 2.12 - Lewis Acids And BasesChapter 3 - An Introduction To Organic Compounds: Nomenclature, Physical Properties, And StructureChapter 3.1 - Alkyl GroupsChapter 3.2 - The Nomenclature Of AlkanesChapter 3.3 - The Nomenclature Of CycloalkanesChapter 3.4 - The Nomenclature Of Alkyl HalidesChapter 3.5 - The Nomenclature Of EthersChapter 3.6 - The Nomenclature Of AlcoholsChapter 3.7 - The Nomenclature Of AminesChapter 3.8 - The Structures Of Alkyl Halides, Alcohols, Ethers, And AminesChapter 3.9 - Noncovalent InteractionsChapter 3.10 - The Solubility Of Organic CompoundsChapter 3.11 - Rotation Occurs About Carbon-carbon Single BondsChapter 3.12 - Some Cycloalkanes Have Angle StrainChapter 3.13 - Conformers Of CyclohexaneChapter 3.14 - Conformers Of Monosubstituted CyclohexanesChapter 3.15 - Conformers Of Disubstituted CyclohexanesChapter 4 - Isomers: The Arrangement Of Atoms In SpaceChapter 4.1 - Cis-trans Isomers Result From Restricted RotationChapter 4.2 - Using The E,z System To Distinguish IsomersChapter 4.3 - A Chiral Object Has A Nonsuperimposable Mirror ImageChapter 4.4 - An Asymmetric Center Is A Cause Of Chirality In A MoleculeChapter 4.5 - Isomers With One Asymmetric CenterChapter 4.6 - Asymmetric Centers And StereocentersChapter 4.7 - How To Draw EnantiomersChapter 4.8 - Naming Enantiomers By The R,s SystemChapter 4.9 - Chiral Compounds Are Optically ActiveChapter 4.10 - How Specific Rotation Is MeasuredChapter 4.11 - Enantiomeric ExcessChapter 4.12 - Compounds With More Than One Asymmetric CenterChapter 4.13 - Stereoisomers Of Cyclic CompoundsChapter 4.14 - Meso Compounds Have Asymmetric Centers But Are Optically InactiveChapter 4.15 - How To Name Isomers With More Than One Asymmetric CenterChapter 4.16 - Nitrogen And Phosphorous Atoms Can Be Asymmetric CentersChapter 4.17 - ReceptorsChapter 5 - Alkenes: Structure, Nomenclature, And An Introduction To Reactivity - Thermodynamics And KineticsChapter 5.1 - Molecular Formulas And The Degree Of UnsaturationChapter 5.2 - The Nomenclature Of AlkenesChapter 5.3 - The Structure Of AlkenesChapter 5.5 - How Alkenes React • Curved Arrows Show The Flow Of ElectronsChapter 5.6 - Thermodynamics: How Much Product Is Formed?Chapter 5.8 - Calculating ??° ValuesChapter 5.9 - Using ??° Values To Determine The Relative Stabilities Of AlkenesChapter 5.10 - Kinetics: How Fast Is The Product Formed?Chapter 5.11 - The Rate Of A Chemical ReactionChapter 5.12 - A Reaction Coordinate Diagram Describes The Energy Changes That Take Place During A ReactionChapter 5.13 - CatalysisChapter 6 - The Reaction Of Alkenes • The Stereochemistry Of Addition ReactionsChapter 6.1 - The Addition Of A Hydrogen Halide To An AlkeneChapter 6.2 - Carbocation Stability Depends On The Number Of Alkyl Groups Attached To The Positively Charged CarbonChapter 6.3 - What Does The Structure Of The Transition State Look Like?Chapter 6.4 - Electrphilic Addition Reactions Are RegioselectiveChapter 6.5 - The Addition Of Water To An AlkeneChapter 6.6 - The Addition Of An Alcohol To An AlkeneChapter 6.7 - A Carbocation Will Rearrange If It Can Form A More Stable CarbocationChapter 6.8 - The Addition Of Borane To An Alkene: Hydroboration-oxidationChapter 6.9 - The Addition Of A Halogen To An AlkeneChapter 6.10 - The Addition Of A Peroxyacid To An AlkeneChapter 6.11 - The Addition Of Ozone To An Alkene: OzonolysisChapter 6.12 - Regioselective, Stereoselective, And Stereospecific ReactionsChapter 6.13 - The Stereochemistry Of Electrophilic Addition ReactionsChapter 6.14 - The Stereochemistry Of Enzyme-catalyzed ReactionsChapter 6.16 - Reactions And SynthesisChapter 7 - The Reaction Of Alkynes • An Introduction To Multistep SynthesisChapter 7.1 - The Nomenclature Of AlkynesChapter 7.2 - How To Name A Compound That Has More Than One Functional GroupChapter 7.3 - The Structure Of AlkynesChapter 7.4 - The Physical Properties Of Unsaturated HydrocarbonsChapter 7.6 - The Addition Of Hydrogen Halides And The Addition Of Halogens To An AlkyneChapter 7.7 - The Addition Of Water To An AlkyneChapter 7.8 - The Addition Of Borane To An Alkyne: Hydroboration-oxidationChapter 7.9 - The Addition Of Hydrogen To An AlkyneChapter 7.10 - A Hydrogen Bonded To An Sp Carbon Is "acidic"Chapter 7.12 - Designing A Synthesis I: An Introduction To Multistep SynthesisChapter 8 - Delocalized Electrons: Their Effect On Stability, Pka, And The Products Of A Reaction • Aromaticity And Electronic Effects: An Introduction To The Reactions Of BenzeneChapter 8.1 - Delocalized Electrons Explain Benzene's StructureChapter 8.4 - How To Draw Resonance ContributorsChapter 8.5 - The Predicted Stabilities Of Resonance ContributorsChapter 8.6 - Delocalization Energy Is The Additional Stability Delocalized Electrons Give To A CompoundChapter 8.7 - Delocalized Electrons Increase StabilityChapter 8.8 - A Molecular Orbital Description Of StabilityChapter 8.9 - Delocalized Electrons Affect Pka ValuesChapter 8.10 - Electronic EffectsChapter 8.11 - Delocalized Electrons Can Affect The Product Of A ReactionChapter 8.12 - Reactions Of DienesChapter 8.13 - Thermodynamic Versus Kinetic ControlChapter 8.14 - The Diels-alder Reaction Is A 1,4-addition ReactionChapter 8.15 - Retrosynthetic Analysis Of The Diels-alder ReactionChapter 8.17 - The Two Criteria For AromaticityChapter 8.18 - Applying The Criteria For AromaticityChapter 8.19 - A Molecular Orbital Description Of AromaticityChapter 8.20 - Aromatic Heterocyclic CompoundsChapter 9 - Substitution And Elimination Reactions Of Alkyl HalidesChapter 9.1 - The Sn2 ReactionChapter 9.2 - Factors That Affect Sn2 ReactionsChapter 9.3 - The Sn1 ReactionChapter 9.4 - Factors That Affect Sn1 ReactionsChapter 9.5 - Competition Between Sn2 And Sn1 ReactionsChapter 9.7 - The E2 ReactionChapter 9.8 - The E1 ReactionChapter 9.9 - Competition Between E2 And E1 ReactionsChapter 9.10 - E2 And E1 Reactions Are StereoselectiveChapter 9.11 - Elimination From Substituted CyclohexanesChapter 9.12 - Predicting The Products Of The Reaction Of An Alkyl Halide With A Nucleophile/baseChapter 9.13 - Benzylic Halides, Allylic Halides, Vinylic Halides, And Aryl HalidesChapter 9.14 - Solvent EffectsChapter 9.15 - Substitution And Elimination Reactions In SynthesisChapter 9.16 - Intermolecular Versus Intramolecular ReactionsChapter 9.17 - Designing A Synthesis Ii: Approaching The ProblemChapter 10 - Reactions Of Alcohols, Ethers, Epoxides, Amines, And Sulfur-containing CompoundsChapter 10.1 - Nucleophilic Substitution Reactions Of Alcohols: Forming Alkyl HalidesChapter 10.2 - Other Methods Used To Convert Alcohols Into Alkyl HalidesChapter 10.3 - Converting An Alcohol Into A Sulfonate EsterChapter 10.4 - Elimination Reactions Of Alcohols: DehydrationChapter 10.5 - Oxidation Of AlcoholsChapter 10.6 - Nucleophilic Substitution Reactions Of EthersChapter 10.7 - Nucleophilic Substitution Reactions Of EpoxidesChapter 10.8 - Arene OxidesChapter 10.9 - Amines Do Not Undergo Substitution Or Elimination ReactionsChapter 10.10 - Quaternary Ammonium Hydroxides Undergo Elimination ReactionsChapter 10.11 - Thiols, Sulfides, And Sulfonium IonsChapter 10.12 - Methylating Agents Used By Chemists Versus Those Used By CellsChapter 11 - Organometallic CompoundsChapter 11.1 - Organolithium And Organomagnesium CompoundsChapter 11.2 - TransmetallationChapter 11.3 - OrganocupratesChapter 11.4 - Palladium-catalyzed Coupling ReactionsChapter 11.5 - Alkene MetathesisChapter 12 - RadicalsChapter 12.2 - The Chlorination And Bromination Of AlkanesChapter 12.3 - Radical Stability Depends On The Number Of Alkyl Groups Attached To The Carbon With The Unpaired ElectronChapter 12.4 - The Distribution Of Products Depends On Probability And ReactivityChapter 12.5 - The Reactivity-selectivity PrincipleChapter 12.6 - Formation Of Explosive PeroxidesChapter 12.7 - The Addition Of Radicals To An AlkeneChapter 12.8 - The Stereochemistry Of Radical Substitution And Radical Addition ReactionsChapter 12.9 - Radical Substitution Of Allylic And Benzylic HydrogensChapter 12.10 - Designing A Synthesis Iii: More Practice With Multistep SynthesisChapter 12.11 - Radical Reactions In Biological SystemsChapter 13 - Mass Spectrometry; Infrared Spectroscopy; Uv/vis SpectroscopyChapter 13.1 - Mass SpectrometryChapter 13.2 - The Mass Spectrum • FragmentationChapter 13.3 - Using The M/z Value Of The Molecular Ion To Calculate The Molecular FormulaChapter 13.4 - Isotopes In Mass SpectrometryChapter 13.5 - High-resolution Mass Spectrometry Can Reveal Molecular FormulasChapter 13.6 - The Fragmentation Patterns Of Functional GroupsChapter 13.9 - Spectroscopy And The Electromagnetic SpectrumChapter 13.13 - The Position Of Absorption BandsChapter 13.14 - The Position And Shape Of An Absorption Band Is Affected By Electron Delocalization And Hydrogen BondingChapter 13.16 - The Absence Of Absorption BandsChapter 13.17 - Some Vibrations Are Infrared InactiveChapter 13.18 - How To Interpret An Infrared SpectrumChapter 13.20 - The Beer-lambert LawChapter 13.21 - The Effect Of Conjugation On ?maxChapter 13.23 - Some Uses Of Uv/vis SpectroscopyChapter 14 - Nmr SpectroscopyChapter 14.1 - An Introduction To Nmr SpectroscopyChapter 14.4 - The Number Of Signals In 1h Nmr SpectrumChapter 14.5 - The Chemical Shift Tells How Far The Signal Is From The Reference SignalChapter 14.6 - The Relative Positions Of 1h Nmr SignalsChapter 14.7 - The Characteristic Values Of Chemical ShiftsChapter 14.8 - Diamagnetic AnisotropyChapter 14.9 - The Integration Of Nmr Signals Reveals The Relative Number Of Protons Causing Each SignalChapter 14.10 - The Splitting Of Signals Is Described By The N+1 RuleChapter 14.11 - What Causes Splitting?Chapter 14.12 - More Examples Of 1h Nmr SpectraChapter 14.13 - Coupling Constants Identify Coupled ProtonsChapter 14.14 - Splitting Diagrams Explain The Multiplicity Of A SignalChapter 14.15 - Enantiotopic And Diastereotopic HydrogensChapter 14.17 - Protons Bonded To Oxygen And NitrogenChapter 14.20 - 13c Nmr SpectroscopyChapter 14.22 - Two-dimensional Nmr SpectroscopyChapter 15 - Reactions Of Carboxylic Acids And Carboxylic Acid DerivativesChapter 15.1 - The Nomenclature Of Carboxylic Acids And Carboxylic Acid DerivativesChapter 15.2 - The Structures Of Carboxylic Acids And Carboxylic Acid DerivativesChapter 15.4 - How Carboxylic Acids And Carboxylic Acid Derivatives ReactChapter 15.5 - The Relative Reactivities Of Carboxylic Acids And Carboxylic Acid DerivativesChapter 15.6 - Reactions Of Acyl ChloridesChapter 15.7 - Reactions Of EstersChapter 15.8 - Acid-catalyzed Ester Hydrolysis And TransesterificationChapter 15.9 - Hydroxide-ion-promoted Ester HydrolysisChapter 15.10 - Reactions Of Carboxylic AcidsChapter 15.11 - Reactions Of AmidesChapter 15.12 - Acid-catalyzed Amide Hydrolysis And AlcoholysisChapter 15.13 - Hydroxide-ion-promoted Hydrolysis Of AmidesChapter 15.14 - Hydrolysis Of An Imide: A Way To Synthesize A Primary AmineChapter 15.15 - NitrilesChapter 15.16 - Acid AnhydridesChapter 15.17 - Dicarboxylic AcidsChapter 15.18 - How Chemists Activate Carboxylic AcidsChapter 16 - Reactions Of Aldehydes And Ketones • More Reactions Of Carboxylic Acid DerivativesChapter 16.1 - The Nomenclature Of Aldehydes And KetonesChapter 16.2 - The Relative Reactivities Of Carbonyl CompoundsChapter 16.4 - Reactions Of Carbonyl Compounds With Carbon NucleophilesChapter 16.5 - Reactions Of Carbonyl Compounds With Hydride IonChapter 16.6 - More About Reduction ReactionsChapter 16.7 - Chemoselective ReactionsChapter 16.8 - Reactions Of Aldehydes And Ketones With Nitrogen NucleophilesChapter 16.9 - Reactions Of Aldehydes And Ketones With Oxygen NucleophilesChapter 16.10 - Protecting GroupsChapter 16.12 - Reaction Of Aldehydes And Ketones With A PeroxyacidChapter 16.13 - The Wittig Reaction Forms An AlkeneChapter 16.14 - Designing A Synthesis Iv: Disconnections, Synthons, And Synthetic EquivalentsChapter 16.15 - Nucleophilic Addition To ?,?-unsaturated Aldehydes And KetonesChapter 16.16 - Nucleophilic Addition To ?,?-unsaturated Carboxylic Acid DerivativesChapter 17 - Reactions At The ?-carbonChapter 17.1 - The Aciidity Of An ?-hydrogenChapter 17.2 - Keto-enol TautomersChapter 17.3 - Keto-enol InterconversionChapter 17.4 - Halogenation Of The ?-carbon Of Aldehydes And KetonesChapter 17.5 - Halogenation Of The ?-carbon Of Carboxylic AcidsChapter 17.6 - Forming An Enolate IonChapter 17.7 - Alkylating The ?-carbonChapter 17.8 - Alkylating And Acylating The ?-carbon Via An Enamine IntermediateChapter 17.9 - Alkylating The ?-carbonChapter 17.10 - An Aldol Addition Forms A ?-hydroxyaldehyde Or A ?-hydroxyketoneChapter 17.11 - The Dehydration Of Aldol Addition Products Forms ?,?-unsaturated Aldehydes And KetonesChapter 17.12 - A Crossed Aldol AdditionChapter 17.13 - A Claisen Condensation Forms A ?-keto EsterChapter 17.14 - Other Crossed CondensationsChapter 17.15 - Intramolecular Condensations And Intramolecular Aldol AdditionsChapter 17.16 - The Robinson AnnulationChapter 17.17 - Co2 Can Be Removed From A Carboxylic Acid That Has A Carbonyl Group At The 3-positionChapter 17.18 - The Malonic Ester Synthesis: A Way To Synthesize A Carboxylic AcidChapter 17.19 - The Acetoacetic Ester Synthesis: A Way To Synthesize A Methyl KetoneChapter 17.20 - Designing A Synthesis V: Making New Carbon-carbon BondsChapter 17.21 - Reactions At The ?-carbon In Living SystemsChapter 18 - Reactions Of Benzene And Substituted BenzenesChapter 18.1 - The Nomenclature Of Monosubstituted BenzenesChapter 18.3 - Halogenation Of BenzeneChapter 18.6 - Friedel-crafts Acylation Of BenzeneChapter 18.7 - Friedel-crafts Alkylation Of BenzeneChapter 18.9 - Using Coupling Reactions To Alkylate BenzeneChapter 18.10 - How Some Substituents On A Benzene Ring Can Be Chemically ChangedChapter 18.11 - The Nomenclature Of Disubstituted And Polysubstituted BenzenesChapter 18.12 - The Effect Of Substituents On ReactivityChapter 18.13 - The Effect Of Substituents On OrientationChapter 18.15 - Additional Considerations Regarding Substituent EffectsChapter 18.16 - Designing A Synthesis Vi: The Synthesis Of Monosubstituted And Disubstituted BenzenesChapter 18.17 - The Synthesis Of Trisubstituted BenzenesChapter 18.18 - Synthesizing Substituted Benzenes Using Arenediazonium SaltsChapter 18.19 - AzobenzenesChapter 18.20 - The Mechanism For The Formation Of A Diazonium IonChapter 18.21 - Nucleophilic Aromatic SubstitutionChapter 18.22 - Designing A Synthesis Vii: The Synthesis Of Cyclic CompoundsChapter 19 - More About Amines • Reactions Of Heterocyclic CompoundsChapter 19.1 - More About NomenclatureChapter 19.2 - More About The Acid-base Properties Of AminesChapter 19.3 - Amines React As Bases And As NucleophilesChapter 19.5 - Aromatic Five-membered-ring HeterocyclesChapter 19.6 - Aromatic Six-membered-ring HeterocyclesChapter 19.7 - Some Heterocyclic Amines Have Important Roles In NatureChapter 20 - The Organic Chemistry Of CarbohydratesChapter 20.1 - Classifying CarbohydratesChapter 20.2 - The D And L NotationChapter 20.3 - The Configurations Of AldosesChapter 20.4 - The Configurations Of KetosesChapter 20.5 - The Reactions Of Monosaccharides In Basic SolutionsChapter 20.6 - Oxidation-reduction Reactions Of MonosaccharidesChapter 20.7 - Lengthening The Chain: The Kiliani-fischer SynthesisChapter 20.8 - Shortening The Chain: The Wohl DegradationChapter 20.9 - The Stereochemistry Of Glucose: The Fischer ProofChapter 20.10 - Monosaccharides Form Cyclic HemiacetalsChapter 20.11 - Glucose Is The Most Stable AldohexoseChapter 20.12 - Formation Of GlycosidesChapter 20.14 - Reducing And Nonreducing SugarsChapter 20.15 - DisaccharidesChapter 20.16 - PolysaccharidesChapter 20.17 - Some Naturally Occuring Compounds Derived From CarbohydratesChapter 20.18 - Carbohydrates On Cell SurfacesChapter 21 - Amino Acids, Peptides, And ProteinsChapter 21.1 - The Nomenclature Of Amino AcidsChapter 21.2 - The Configuration Of Amino AcidsChapter 21.3 - Acid-base Properties Of Amino AcidsChapter 21.4 - The Isoelectric PointChapter 21.5 - Separating Amino AcidsChapter 21.6 - Synthesis Of Amiino AcidsChapter 21.7 - Resolution Of Racemic Mixtures Of Amino AcidsChapter 21.8 - Peptide Bonds And Disulfide BondsChapter 21.9 - Some Interesting PeptidesChapter 21.10 - The Strategy Of Peptide Bond Synthesis: N-protection And C-activationChapter 21.11 - Automated Peptide SynthesisChapter 21.13 - How To Determine The Primary Structure Of A Polypeptide Or A ProteinChapter 21.14 - Secondary StructureChapter 21.15 - Tertiary StructureChapter 21.16 - Quaternary StructureChapter 21.17 - Protein DenaturationChapter 22 - Catalysis In Organic Reactions And In Enzymatic ReactionsChapter 22.2 - Acid CatalysisChapter 22.3 - Base CatalysisChapter 22.5 - Metal-ion CatalysisChapter 22.6 - Intramolecular ReactionsChapter 22.7 - Intramolecular CatalysisChapter 22.9 - An Enzyme-catalyzed Reaction That Is Reminiscent Of Acid-catalyzed Amide HydrolysisChapter 22.10 - Another Enzyme-catalyzed Reaction That Is Reminiscent Of Acid-catalyzed Amide HydrolysisChapter 22.11 - An Enzyme-catalyzed Reaction That Involves Two Sequential Sn2 ReactionsChapter 22.12 - An Enzyme-catalyzed Reaction That Is Reminiscent Of The Base-catalyzed Enediol RearrangementChapter 22.13 - Another Enzyme-catalyzed Reaction That Is Reminiscent Of A Retro-aldol AdditionChapter 23 - The Organic Chemistry Of The Coenzymes, Compounds Derived From VitaminsChapter 23.1 - Niacin: The Vitamin Needed For Many Redox ReactionsChapter 23.2 - Riboflavin: Another Vitamin Used In Redox ReactionsChapter 23.3 - Vitamin B1: The Vitamin Needed For Acyl Group TransferChapter 23.5 - Vitamin B6: The Vitamin Needed For Amino Acid TransformationsChapter 23.6 - Vitamin B12: The Vitamin Needed For Certain IsomerizationsChapter 23.7 - Folic Acid: The Vitamin Needed For One-carbon TransferChapter 23.8 - Vitamin K: The Vitamin Needed For Carboxylation Of GlutamateChapter 24 - The Organic Chemistry Of The Metabolic PathwaysChapter 24.3 - The "high-energy" Character Of Phosphoanhydride BondsChapter 24.5 - The Catabolixm Of Fats: Stages 1 And 2Chapter 24.6 - The Catabolixm Of Carbohydrates: Stages 1 And 2Chapter 24.7 - The Fats Of PyruvateChapter 24.8 - The Catabolism Of Proteins: Stages 1 And 2Chapter 24.9 - The Citric Acid Cycle: Stage 3Chapter 24.10 - Oxidative Phosphorylation: Stage 4Chapter 24.12 - GluconeogenesisChapter 24.14 - Amino Acid BiosynthesisChapter 25 - The Organic Chemistry Of LipidsChapter 25.1 - Fatty Acids Are Long-chain Carboxylic AcidsChapter 25.3 - Fats And Oils Are TriglyveridesChapter 25.5 - Phospholipids Are Components Of Cell MembranesChapter 25.6 - Prostaglandins Regulate Physiological ResponsesChapter 25.7 - Terpenes Contain Carbon Atoms In Multiples Of FiveChapter 25.8 - How Terpenes Are BiosynthesizedChapter 25.9 - How Nature Synthesizes CholesterolChapter 25.10 - SteroidsChapter 26 - The Chemistry Of The Nucleic AcidsChapter 26.1 - Nucleosides And NucleotidesChapter 26.3 - The Secondary Structure Of DnaChapter 26.4 - Why Dna Does Not Have A 2'-oh GroupChapter 26.5 - The Biosynthesis Of Dna Is Called ReplicationChapter 26.7 - The Biosynthesis Of Rna Is Called TranscriptionChapter 26.9 - The Biosynthesis Of Proteins Is Called TranslationChapter 26.10 - Why Dna Contains Thymine Instead Of UracilChapter 26.12 - How The Base Sequence Of Dna Is DeterminedChapter 27 - Synthetic PolymersChapter 27.3 - Radical PolymerizationChapter 27.4 - Cationic PolymerizationChapter 27.5 - Anionic PolymerizationChapter 27.6 - Ring-opening PolymerizationChapter 27.8 - Polymerization Of DienesChapter 27.11 - Classes Of Step-growth PolymersChapter 27.12 - Physical Properties Of PolymersChapter 27.13 - Recycling PolymersChapter 28 - Pericyclic ReactionsChapter 28.1 - There Are Three Kinds Of Pericyclic ReactionsChapter 28.2 - Molecular Orbitals And Orbital SymmetryChapter 28.3 - Electrocyclic ReactionsChapter 28.4 - Cycloaddition ReactionsChapter 28.5 - Sigmatropic RearrangementsChapter 28.6 - Pericyclic Reactions In Biological SystemsChapter 28.7 - Summary Of The Selection Rules For Pericyclic Reactions

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