Organic Chemistry As a Second Language: First Semester Topics - 4th Edition - by David R. Klein - ISBN 9781119110668

Organic Chemistry As a Second Language:...
4th Edition
David R. Klein
Publisher: WILEY
ISBN: 9781119110668

Solutions for Organic Chemistry As a Second Language: First Semester Topics

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Chapter 2.8 - Assessing The Relative Importance Of Resonance StructuresChapter 3.1 - Factor 1 - What Atom Is The Charge On?Chapter 3.2 - Factor 2 - ResonanceChapter 3.3 - Factor 3 - InductionChapter 3.5 - Ranking The Four FactorsChapter 3.8 - Predicting The Position Of EquilibriumChapter 3.9 - Showing A MechanismChapter 4.1 - Orbitals And Hybridization StatesChapter 4.2 - GeometryChapter 4.3 - Lone PairsChapter 5.1 - Functional GroupChapter 5.2 - UnsaturationChapter 5.3 - Naming The Parent ChainChapter 5.4 - Naming SubstituentsChapter 5.5 - StereoisomerismChapter 5.6 - NumberingChapter 6.1 - How To Draw A Newman ProjectionChapter 6.2 - Ranking The Stability Of Newman ProjectionChapter 6.4 - Placing Groups On The ChairChapter 6.5 - Ring FlippingChapter 6.6 - Comparing The Stability Of ChairsChapter 7.1 - Locating StereocentersChapter 7.2 - Determining The Configuration Of A StereocenterChapter 7.3 - NomenclatureChapter 7.4 - Drawing EnantiomersChapter 7.5 - DiastereomersChapter 7.6 - Meso CompoundsChapter 7.7 - Drawing Fischer ProjectionsChapter 8.2 - Nucleophiles And ElectrophilesChapter 8.3 - Basicity Vs, NucleophilicityChapter 8.4 - Arrow-pushing Patterns For Ionic MechanismsChapter 8.5 - Carbocation RearrangementsChapter 9.2 - Factor 1-the Electrophile(substrate)Chapter 9.3 - Factor 2-the NucleophileChapter 9.4 - Factor 3-the Leaving GroupChapter 9.5 - Factor 4-the SolventChapter 9.6 - Using All Four FactorsChapter 10.2 - The Regiochemical Outcome Of An E2 ReactionChapter 10.3 - The Stereochemical Outcome Of An E2 ReactionChapter 10.5 - The Regiochemical Outcome Of An E1 ReactionChapter 10.8 - Determining The Function Of The ReagentChapter 10.9 - Identifying The Mechanism(s)Chapter 10.10 - Predicting The ProductsChapter 11.1 - Terminology Describing RegiochemistryChapter 11.2 - Terminology Describing StereochemistryChapter 11.3 - Adding H And HChapter 11.4 - Adding H And X, MarkovnikovChapter 11.5 - Adding H And Br, Anti-markovnikovChapter 11.6 - Adding H And Oh, MarkovnikovChapter 11.7 - Adding H And Oh, Anti-markovnikovChapter 11.8A - One-step SynthesesChapter 11.8B - Changing The Position Of A Leaving GroupChapter 11.8C - Changing The Position Of A π BondChapter 11.8D - Introducing FunctionalityChapter 11.9 - Adding Br And Br; Adding Br And OhChapter 11.10 - Adding Oh And Oh, AntiChapter 11.11 - Adding Oh And Oh, SynChapter 11.12 - Oxidative Cleavage Of An AlkeneChapter 12.1 - Structure And Properties Of AlkynesChapter 12.2 - Preparation Of AlkynesChapter 12.3 - Alkylation Of Terminal AlkynesChapter 12.4 - Reduction Of AlkynesChapter 12.5 - Hydration Of AlkynesChapter 12.6 - Keto-enol TautomerizationChapter 12.7 - Ozonolysis Of AlkynesChapter 13.1 - Naming And Designating AlcoholsChapter 13.2 - Predicting Solubility Of AlcoholsChapter 13.3 - Predicting Relative Acidity Of AlcoholsChapter 13.4 - Preparing Alcohols: A ReviewChapter 13.5 - Preparing Alcohols Via ReductionChapter 13.6 - Preparing Alcohols Via Grignard ReactionChapter 13.7 - Summary Of Methods For Preparing AlcoholsChapter 13.8 - Reaction Of Alcohols: Substitution And EliminationChapter 13.9 - Reaction Of Alcohols: OxidationChapter 13.10 - Converting An Alcohol Into An EtherChapter 14.1 - Introduction To EthersChapter 14.2 - Preparation Of EthersChapter 14.3 - Reactions Of EthersChapter 14.4 - Preparation Of EpoxidesChapter 14.5 - Ring-opening Reactions Of Epoxides

Book Details

Readers continue to turn to Klein's Organic Chemistry as a Second Language: First Semester Topics, 4th Edition because it enables them to better understand fundamental principles, solve problems, and focus on what they need to know to succeed. This edition explores the major principles in the field and explains why they are relevant. It is written in a way that clearly shows the patterns in organic chemistry so that readers can gain a deeper conceptual understanding of the material. Topics are presented clearly in an accessible writing style along with numerous hands-on problem solving exercises.

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