ORGANIC CHEM F/UT (LOOSELEAF)8th EditionVOLLHARDT Publisher: Macmillan Higher EducationISBN: 9781319242619
ORGANIC CHEM F/UT (LOOSELEAF)
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Chapter 1 - Structure And Bonding In Organic MoleculesChapter 1.3 - Ionic And Covalent Bonds: The Octet RuleChapter 1.4 - Electron-dot Model Of Bonding: Lewis StructuresChapter 1.5 - Resonance FormsChapter 1.6 - Atomic Orbitals: A Quantum Mechanical Description Of Electrons Around The NucleusChapter 1.7 - Molecular Orbitals And Covalent BondingChapter 1.8 - Hybrid Orbitals: Bonding In Complex MoleculesChapter 1.9 - Structures And Formulas Of Organic MoleculesChapter 2 - Structure And ReactivityChapter 2.1 - Kinetics And Thermodynamics Of Simple Chemical Processes
Chapter 2.2 - Keys To Success: Using Curved “electron-pushing” Arrows To Describe Chemical ReactionsChapter 2.3 - Acids And BasesChapter 2.5 - Straight-chain And Branched AlkanesChapter 2.6 - Naming The AlkanesChapter 2.7 - Structural And Physical Properties Of AlkanesChapter 2.9 - Rotation In Substituted EthanesChapter 3 - Reactions Of AlkanesChapter 3.1 - Strength Of Alkane Bonds: RadicalsChapter 3.4 - Chlorination Of Methane: The Radical Chain MechanismChapter 3.5 - Other Radical Halogenations Of MethaneChapter 3.7 - Chlorination Of Higher Alkanes: Relative Reactivity And SelectivityChapter 3.9 - Synthetic Radical HalogenationChapter 3.11 - Combustion And The Relative Stabilities Of AlkanesChapter 4 - CycloalkanesChapter 4.1 - Names And Physical Properties Of CycloalkanesChapter 4.2 - Ring Strain And The Structure Of CycloalkanesChapter 4.3 - Cyclohexane: A Strain-free CycloalkaneChapter 4.4 - Substituted CyclohexanesChapter 4.6 - Polycyclic AlkanesChapter 4.7 - Carbocyclic Products In NatureChapter 5 - StereoisomersChapter 5.1 - Chiral MoleculesChapter 5.2 - Optical ActivityChapter 5.3 - Absolute Configuration: R,s Sequence RulesChapter 5.4 - Fischer ProjectionsChapter 5.5 - Molecules Incorporating Several Stereocenters: DiastereomersChapter 5.6 - Meso CompoundsChapter 5.7 - Stereochemistry In Chemical ReactionsChapter 6 - Properties And Reactions Of HaloalkanesChapter 6.2 - Nucleophilic SubstitutionChapter 6.3 - Reaction Mechanisms Involving Polar Functional Groups: Using “electron-pushing” ArrowsChapter 6.4 - A Closer Look At The Nucleophilic Substitution Mechanism: KineticsChapter 6.5 - Frontside Or Backside Attack? Stereochemistry Of The Sn2 ReactionChapter 6.6 - Consequences Of Inversion In Sn2 ReactionsChapter 6.7 - Structure And Sn2 Reactivity: The Leaving GroupChapter 6.8 - Structure And Sn2 Reactivity: The NucleophileChapter 6.9 - Keys To Success: Choosing Among Multiple Mechanistic PathwaysChapter 6.10 - Structure And Sn2 Reactivity: The SubstrateChapter 7 - Further Reactions Of HaloalkanesChapter 7.1 - Solvolysis Of Tertiary And Secondary HaloalkanesChapter 7.2 - Unimolecular Nucleophilic SubstitutionChapter 7.3 - Stereochemical Consequences Of Sn1 ReactionsChapter 7.4 - Effects Of Solvent, Leaving Group, And Nucleophile On Unimolecular SubstitutionChapter 7.5 - Effect Of The Alkyl Group On The Sn1 Reaction: Carbocation StabilityChapter 7.6 - Unimolecular Elimination: E1Chapter 7.7 - Bimolecular Elimination: E2Chapter 7.8 - Keys To Success: Substitution Versus Elimination—structure Determines FunctionChapter 7.9 - Summary Of Reactivity Of HaloalkanesChapter 8 - Hydroxy Functional Group: AlcoholsChapter 8.1 - Naming The AlcoholsChapter 8.3 - Alcohols As Acids And BasesChapter 8.4 - Synthesis Of Alcohols By Nucleophilic SubstitutionChapter 8.5 - Synthesis Of Alcohols: Oxidation–reduction Relation Between Alcohols And Carbonyl CompoundsChapter 8.6 - Organometallic Reagents: Sources Of Nucleophilic Carbon For Alcohol SynthesisChapter 8.7 - Organometallic Reagents In The Synthesis Of AlcoholsChapter 8.8 - Keys To Success: An Introduction To Synthetic StrategyChapter 9 - Further Reactions Of Alcohols And The Chemistry Of EthersChapter 15 - Benzene And Aromaticity
Sample Solutions for this Textbook
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To draw the Lewis structure, calculate total number of valence electrons. Draw these valence...Total enthalpy of “oven and room” remains unchanged because as pizza is brought out system (oven)...The carbon linked to one alkyl/carbon while other two H are termed primary carbon. Thus hydrogen...Considering the structural formula C5H10 with a ring, the maximum number of carbon in that ring can...Structures of cyclopropylcyclopentane and cyclobutylcyclobutane are illustrated as follows: The...CH3CH2Cl has only two carbons. Therefore, parent carbon chain is named as ethane. A chlorine atom is...The given reaction is an example of solvolysis reaction. In the solvolysis reaction, the solvent...The given organic compound is as follows: The name of the compound is 2-butanol. Here, hydroxyl...In the given structure, there is an aromatic ring with –COOH and -Cl group. Since –COOH group is...
More Editions of This Book
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EBK ORGANIC CHEMISTRY
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EBK STUDY GUIDE/SOLUTIONS MANUAL FOR OR
8th Edition
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Organic Chemistry: Structure and Function
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