ORGANIC CHEMISTRY GGC>CUSTOM<-TEXT2nd EditionKlein Publisher: WILEYISBN: 9781119288510
ORGANIC CHEMISTRY GGC>CUSTOM<-TEXT
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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 - Vsepr Theory: Predicting GeometryChapter 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 2.4 - Carbon Atoms With Formal ChargesChapter 2.5 - Identifying Lone PairsChapter 2.6 - Three-dimensional Bond-line StructuresChapter 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 - 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 And VropaneChapter 4.8 - Conformational Analysis Of ButaneChapter 4.11 - Drawing Chair ConformationsChapter 4.12 - Monusubstituted 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 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 - Substitution ReactionsChapter 7.2 - Alkyl HalidesChapter 7.3 - Possible Mechanisms For Substitution ReactionsChapter 7.4 - The Sn2 MechanismChapter 7.5 - The Sn1 MechanismChapter 7.6 - Drawing The Complete Mechanism Of An Sn1 ReactionChapter 7.7 - Drawing The Complete Mechanism Of An Sn2 ReactionChapter 7.8 - Determining Which Mechanism PredominatesChapter 7.9 - Selecting Reagents To Accomplish Functional Group TransformationChapter 8 - Alkenes: Structure And Preparation Via Elimination ReactionsChapter 8.3 - Nomenclature Of AlkenesChapter 8.4 - Stereoisomerism In AlkenesChapter 8.5 - Alkene StabilityChapter 8.6 - Possible Mechanisms For EliminatlonChapter 8.7 - The E2 MechanismChapter 8.8 - Drawing The Products Of An E2 ReactionChapter 8.9 - The E1 MechanismChapter 8.10 - Drawing The Complete Mechanism Of An E1 ProcessChapter 8.11 - Drawing The Complete Mechanism Of An E2 ProcessChapter 8.12 - Substitution Vs. Elimination: Identifying The ReagentChapter 8.13 - Substitution Vs. Elimination: Identifying The Mechanism(s)Chapter 8.14 - Substitution Vs. Elimination: Predicting The ProductsChapter 9 - Addition Reactions Of AlkenesChapter 9.3 - HydrohalogenationChapter 9.4 - Acid-catalyzed HydrationChapter 9.6 - Hydroboration-oxidationChapter 9.7 - Catalytic HydrogenationChapter 9.8 - Halogenation And Halohydrin FormationChapter 9.9 - Anti DihydroxylationChapter 9.10 - Syn DihydroxylationChapter 9.11 - Oxidative OeavageChapter 9.12 - Predicting Products Of An Addition ReactionChapter 9.13 - Synthesis StrategiesChapter 10 - AlkynesChapter 10.2 - Nomenclature Of AlkynesChapter 10.3 - Acidity Of Acetylene And Terminal AlkynesChapter 10.4 - Preparing AlkynesChapter 10.5 - Reduction Of AlkynesChapter 10.6 - Hydrohalogenation Of AlkynesChapter 10.7 - Hydration Of AlkynesChapter 10.9 - Ozonolysis Of AlkynesChapter 10.10 - Alkylation Of Terminal AlkynesChapter 10.11 - Synthesis StrategiesChapter 11 - Radical ReactionsChapter 11.1 - RadicalsChapter 11.2 - Common Patterns In Radical MechanismsChapter 11.3 - Chlorination Of MethaneChapter 11.5 - Selectivity Of HalogenationChapter 11.6 - Stereochemistry Of HalogenationChapter 11.7 - Allylic BrominationChapter 11.8 - Atmospheric Chemistry And The Ozone LayerChapter 11.9 - Autooxidation And AntioxidantsChapter 11.10 - Radical Addition Of Hbr: Anti-markovnikov AdditionChapter 12 - SynthesisChapter 12.1 - One-step SynthesesChapter 12.2 - Functional Group TransformationsChapter 12.3 - Reactions That Change The Carbon SkeletonChapter 12.4 - How To Approach A Synthesis ProblemChapter 12.5 - Retrosynthetic AnalysisChapter 13 - Alcohols And PhenolsChapter 13.1 - Structure And Properties Of AlcoholsChapter 13.2 - Acidity Of Alcohols And PhenolsChapter 13.3 - Preparation Of Alcohols Via Substitution Or AdditionChapter 13.4 - Preparation Of Alcohols Via ReductionChapter 13.6 - Preparation Of Alcohols Via Grignard ReagentsChapter 13.7 - Protection Of AlcoholsChapter 13.9 - Reactions Of Alcohols: Substitution And EliminationChapter 13.10 - Reactions Of Alcohols: OxidationChapter 13.13 - Synthesis StrategiesChapter 14 - Ethers And Epoxides; Thiols And SulfidesChapter 14.2 - Nomenclature Of EthersChapter 14.4 - Crown EthersChapter 14.5 - Preparation Of EthersChapter 14.6 - Reactions Of EthersChapter 14.7 - Nomenclature Of EpoxidesChapter 14.8 - Preparation Of EpoxidesChapter 14.9 - Enantioselective EpoxidationChapter 14.10 - Ring-opening Reactions Of EpoxidesChapter 14.11 - Thiols And SulfidesChapter 14.12 - Synthesis Strategies Involving EpoxidesChapter 15 - Infrared Spectroscopy And Mass SpectrometryChapter 15.3 - Signal Characteristics: WavenumberChapter 15.4 - Signal Characteristics: IntensityChapter 15.5 - Signal Characteristics: ShapeChapter 15.6 - Analyzing An Ir SpectrumChapter 15.7 - Using Ir Spectroscopy To Distinguish Between Two CompoundsChapter 15.9 - Analyzing The (m)+· PeakChapter 15.10 - Analyzing The (m+1)+· PeakChapter 15.11 - Analyzing The (m+2)+· PeakChapter 15.12 - Analyzing The FragmentsChapter 15.13 - High Resolution Mass SpectrometryChapter 15.16 - Hydrogen Deficiency Index: Degrees Of UnsaturationChapter 16 - Nuclear Magnetic Resonance SpectroscopyChapter 16.4 - Number Of SignalsChapter 16.5 - Chemical ShiftChapter 16.6 - IntegrationChapter 16.7 - MultiplicityChapter 16.8 - Drawing The Expected 1h Nmr Spectrum Of A CompoundChapter 16.9 - Using 1h Nmr Spectroscopy To Distinguish Between CompoundsChapter 16.10 - Analyzing A 1h Nmr SpectrumChapter 16.12 - Chemical Shifts In 13c Nmr SpectroscopyChapter 16.13 - Dept 13c Nmr SpectroscopyChapter 17 - Conjugated Pi Systems And Pericyclic ReactionsChapter 17.1 - Classes Of DienesChapter 17.2 - Conjugated DienesChapter 17.3 - Molecular Orbital TheoryChapter 17.4 - Electrophilic AdditionChapter 17.5 - Thermodynamic Control Vs. Kinetic ControlChapter 17.7 - Diels-alder ReactionsChapter 17.8 - Mo Description Of CycloadditionsChapter 17.9 - Electrocyclic ReactionsChapter 17.10 - Sigmatropic RearrangementsChapter 17.11 - Uv-vis SpectroscopyChapter 17.12 - ColorChapter 18 - Aromatic CompoundsChapter 18.2 - Nomenclature Of Benzene DerivativesChapter 18.4 - Stability Of BenzeneChapter 18.5 - Aromatic Compounds Other Than BenzeneChapter 18.6 - Reactions At The Benzylic PositionChapter 18.7 - Reduction Of The Aromatic MoietyChapter 18.8 - Spectroscopy Of Aromatic CompoundsChapter 19 - Aromatic Substitution ReactionsChapter 19.2 - HalogenationChapter 19.3 - SulfonationChapter 19.4 - NitrationChapter 19.5 - Friedel-crafts AlkylationChapter 19.6 - Friedel-crafts AcylationChapter 19.7 - Activating GroupsChapter 19.8 - Deactivating GroupsChapter 19.9 - Halogens: The ExceptionChapter 19.10 - Determining The Directing Effects Of A SubstituentChapter 19.11 - Multiple SubstituentsChapter 19.12 - Synthesis StrategiesChapter 19.13 - Nucleophilic Aromatic SubstitutionChapter 19.14 - Elimination-additionChapter 19.15 - Identifying The Mechanism Of An Aromatic Substitution ReactionChapter 20 - Aldehydes And KetonesChapter 20.2 - NomenclatureChapter 20.3 - Preparing Aldehydes And Ketones: A ReviewChapter 20.4 - Introduction To Nucleophilic Addition ReactionsChapter 20.5 - Oxygen NucleophilesChapter 20.6 - Nitrogen NucleophilesChapter 20.7 - Hydrolysis Of Acetals, Lmines, And EnaminesChapter 20.8 - Sulfur NucleophilesChapter 20.9 - Hydrogen NucleophilesChapter 20.10 - Carbon NucleophilesChapter 20.11 - Baeyer-villiger Oxidation Of Aldehydes And KetonesChapter 20.12 - Synthesis StrategiesChapter 20.13 - Spectroscopic Analysis Of Aldehydes And KetonesChapter 21 - Carboxylic Acids And Their DerivativesChapter 21.2 - Nomenclature Of Carboxylic AcidsChapter 21.3 - Structure And Properties Of Carboxylic AcidsChapter 21.4 - Preparation Of Carboxylic AcidsChapter 21.5 - Reactions Of Carboxylic AcidsChapter 21.6 - Introduction To Carboxylic Acid DerivativesChapter 21.7 - Reactivity Of Carboxylic Acid DerivativesChapter 21.8 - Preparation And Reactions Of Acid ChloridesChapter 21.9 - Preparation And Reactions Of Acid AnhydridesChapter 21.10 - Preparation Of EstersChapter 21.11 - Reactions Of EstersChapter 21.12 - Preparation And Reactions Of AmidesChapter 21.13 - Preparation And Reactions Of NitrilesChapter 21.14 - Synthesis StrategiesChapter 21.15 - Spectroscopy Of Carboxylic Acids And Their DerivativesChapter 22 - Alpha Carbon Chemistry: Enols And EnolatesChapter 22.1 - Introduction To Alpha Carbon Chemistry: Enols And EnolatesChapter 22.2 - Alpha Halogenation Of Enols And EnolatesChapter 22.3 - Aldol ReactionsChapter 22.4 - Claisen CondensationsChapter 22.5 - Alkylation Of The Alpha PositionChapter 22.6 - Conjugate Addition ReactionsChapter 22.7 - Synthesis StrategiesChapter 23 - AminesChapter 23.2 - Nomenclature Of AminesChapter 23.3 - Properties Of AminesChapter 23.4 - Preparation Of Amines: A ReviewChapter 23.5 - Preparation Of Amines Via Substitution ReactionsChapter 23.6 - Preparation Of Amines Via Reductive AminationChapter 23.7 - Synthesis StrategiesChapter 23.8 - Acylation Of AminesChapter 23.9 - The Hofmann EliminationChapter 23.10 - Reactions Of Amines With Nitrous AcidChapter 23.11 - Reactions Of Aryldiazonium IonsChapter 23.12 - Nitrogen HeterocyclesChapter 23.13 - Spectroscopy Of AminesChapter 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 GGC>CUSTOM<-TEXT homework problems. See examples below:
Carbon (C), hydrogen (H) valency in C4H10 Carbon is tetravalent whereas hydrogen is monovalent...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...The longest chain of the given compounds is identified by counting the number of carbon atoms...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...To identify: The systematic name for the given structure (a). Draw the given molecule (a) and find...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...For the given compound A the responsible bonds are, Conjugated carbonyl and conjugated C=C bonds....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...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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ISBN: 9781118795675
Organic Chemistry: WileyPLUS Student Package (Wiley Plus Products)
2nd Edition
ISBN: 9781118452301
Student Study Guide and Solutions Manual to accompany Organic Chemistry, Binder Ready Version
2nd Edition
ISBN: 9781118700815
Organic Chemistry 2E Binder Ready Version with SSM/SG BRV and WileyPLUS Card Set (Wiley Plus Products)
2nd Edition
ISBN: 9781118941645
Organic Chemistry, Binder Ready Version
2nd Edition
ISBN: 9781118454312
Wileyplus Access Code W/ Online Text Included
2nd Edition
ISBN: 9781118863053
Organic Chemistry 2E All Access Pack
2nd Edition
ISBN: 9781118872840
Student Study Guide and Solutions Manual T/A Organic Chemistry
2nd Edition
ISBN: 9781118647950
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