ORGANIC CHEMISTRY-PRINT COMPANION (LL)3rd EditionKlein Publisher: WILEYISBN: 9781119444251
ORGANIC CHEMISTRY-PRINT COMPANION (LL)
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Chapter 1 - A Review Of General Chemistry: Electrons, Bonds, And Molecular PropertiesChapter 1.2 - The Structural Theory Of MatterChapter 1.3 - Electrons, Bonds, And Lewis StructuresChapter 1.4 - Identifying Formal ChargesChapter 1.5 - Induction And Polar Covalent BondsChapter 1.6 - Atomic OrbitalsChapter 1.9 - Hybridized Atomic OrbitalsChapter 1.10 - Predicting Molecular Geometry: Vsepr TheoryChapter 1.11 - Dipole Moments And Molecular PolarityChapter 1.12 - Intermolecular Forces And Physical Properties
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
Sample Solutions for this Textbook
We offer sample solutions for ORGANIC CHEMISTRY-PRINT COMPANION (LL) homework problems. See examples below:
Given molecular formula C6H14 is, Carbon is tetravalent and hydrogen is monovalent. Since Carbon is...Explanation: To draw all carbon atoms for given bond-line structures of compounds. Put a carbon atom...Explanation: The most acidic proton of the given acid (a) is O-H proton, because deprotonation at...In the given compound, the longest carbon chain (highlighted with bold lines) contains EIGHT carbons...Explanation: Draw the structure of the given molecule and find the chiral centers. Chiral centers of...Explanation: To find: Bond-dissociation energy of the given compounds. Draw the given molecule and...Explanation: To identify: The systematic name and the common name for the given molecules. Find the...Explanation: To explain: the conditions for the given reaction. Given reaction is shown below. Clear...Explanation: The systematic name for the given molecule (a). Draw the given molecule (a) and find...
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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