Book
xii, 1161 pages : illustrations ; 29 cm
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD271 .L495 2016 Unavailable At bindery Request
Book
xvi, 355 pages : illustrations ; 25 cm
  • Preface to the Third Edition xi Preface to the Second Edition xiii Preface to the First Edition xv 1 Reading Nomenclature 1 1.1 Acyclic Polyfunctional Molecules 2 1.2 Monocyclic Aliphatic Compounds 3 1.3 Bridged Polycyclic Structures 4 1.4 Fused Polycyclic Compounds 6 1.5 Spiro Compounds 10 1.6 Monocyclic Heterocyclic Compounds 12 1.7 Fused ]Ring Heterocyclic Compounds 14 1.8 Bridged and Spiro Heterocyclic Compounds 19 Resources 20 Problems 21 References 22 2 Accessing Chemical Information 25 2.1 Databases 25 2.2 Chemical Literature 26 2.3 Synthetic Procedures 29 2.4 Health and Safety Information 30 Problems 32 References 33 3 Stereochemistry 35 3.1 Representations 35 3.2 Vocabulary 37 3.3 Property Differences Among Stereoisomers 40 3.4 Resolution of Enantiomers 44 3.5 Enantioselective Synthesis 47 3.6 Reactions at a Stereogenic Atom 49 3.6.1 Racemization 49 3.6.2 Epimerization 50 3.6.3 Inversion 51 3.6.4 Retention 51 3.6.5 Transfer 52 3.7 Relative and Absolute Configuration 53 3.8 Topism 56 Resources 59 Problems 60 References 65 4 Mechanisms and Predictions 69 4.1 Reaction Coordinate Diagrams and Mechanisms 69 4.2 The Hammond Postulate 71 4.3 Methods for Determining Mechanisms 72 4.3.1 Identification of Products and Intermediates 72 4.3.2 Isotope Tracing 73 4.3.3 Stereochemical Determination 74 4.3.4 Concentration Dependence of Kinetics 75 4.3.5 Isotope Effects in Kinetics 85 4.3.6 Temperature Effects on Kinetics 87 4.3.7 Substituent Effects on Kinetics 90 4.4 Representative Mechanisms 95 4.4.1 Reactions in Basic Solution 96 4.4.2 Reactions in Acidic Solution 100 4.4.3 Free ]Radical Reactions 103 4.4.4 Molecular Rearrangements 106 Resources 108 Problems 109 References 120 5 Electron Delocalization, Aromatic Character, and Pericyclic Reactions 123 5.1 Molecular Orbitals 124 5.2 Aromatic Character 130 5.3 Pericyclic Reactions 135 5.3.1 Cycloaddition Reactions 137 5.3.2 Electrocyclic Reactions 142 5.3.3 Sigmatropic Reactions 147 Resources 152 Problems 152 References 158 6 Functional Group Transformations 163 6.1 Carboxylic Acids and Related Derivatives 164 6.1.1 Carboxylic Acids 164 6.1.2 Carboxylic Esters 166 6.1.3 Carboxylic Amides 168 6.1.4 Carboxylic Acid Halides 168 6.1.5 Carboxylic Anhydrides 169 6.1.6 Nitriles 169 6.1.7 O rtho Esters 170 6.2 Aldehydes, Ketones, and Derivatives 171 6.2.1 Aldehydes 171 6.2.2 Ketones 174 6.2.3 Imines and Enamines 175 6.2.4 Acetals 175 6.2.5 Vinyl Ethers 177 6.3 Alcohols 179 6.4 Ethers 179 6.5 Alkyl Halides 181 6.5.1 Alkyl Chlorides and Alkyl Bromides 182 6.5.2 Alkyl Iodides 184 6.5.3 Alkyl Fluorides 184 6.6 Amines 185 6.7 Isocyanates 187 6.8 Alkenes 187 6.9 Reductive Removal of Functionality 190 Resources 191 Problems 191 References 198 7 Carbon Carbon Bond Formation 205 7.1 Carbon Carbon Single Bond Formation 206 7.1.1 Reactions in Basic Solution 206 7.1.2 Reactions in Acidic Solution 214 7.1.3 O rganometallic Coupling Reactions 217 7.2 Carbon Carbon Double ]Bond Formation 218 7.3 Multibond Processes 222 Resources 224 Problems 224 References 230 8 Planning Multistep Syntheses 235 8.1 Retrosynthetic Analysis 235 8.2 Disconnection at a Functional Group or Branch Point 236 8.3 Cooperation for Difunctionality 244 8.4 Ring Closure 250 8.5 Acetylide Alkylation and Addition 253 8.6 T he Diels Alder Reaction 255 8.7 T he Claisen Rearrangement 259 8.8 Synthetic Strategies 263 8.9 Final Note 265 Resources 266 Problems 266 References 271 9 Physical Influences on Reactions 277 9.1 Unimolecular Reactions 278 9.2 Homogenous Two ]Component Reactions 279 9.3 Temperature Effects 280 9.4 Pressure Effects 281 9.5 Solvent Effects 282 9.6 Biphasic Reactions 283 9.6.1 Phase Transfer Catalysis 283 9.6.2 Increasing Solubility 286 9.6.3 Increasing Surface Area 287 9.6.4 Ultrasound 287 9.7 Reactions on Chemical Supports 288 9.8 Using Unfavorable Equilibria 291 9.9 Green Chemistry 293 Resources 294 Problems 294 References 295 10 Survey of Organic Spectroscopy 299 10.1 Electromagnetic Radiation 299 10.2 Ultraviolet Spectroscopy 300 10.2.1 Origin of the Signals 300 10.2.2 Interpretation 302 10.2.3 Visible Spectroscopy 302 10.3 Infrared Spectroscopy 303 10.3.1 Origin of the Signals 304 10.3.2 Interpretation 304 10.4 Mass Spectrometry 305 10.4.1 Origin of the Signals 306 10.4.2 Interpretation 307 10.5 N MR Spectroscopy 309 10.5.1 Origin of the Signals 309 10.5.2 Interpretation of Proton NMR Spectra 311 10.6 Carbon NMR Spectra 323 10.6.1 General Characteristics 323 10.6.2 Interpretation of 13C NMR Spectra 325 10.7 Correlation of 1H and 13C NMR Spectra 327 Resources 329 Problems 329 References 333 Appendix A 337 Appendix B 341 Index 347.
  • (source: Nielsen Book Data)
This book presents key aspects of organic synthesis stereochemistry, functional group transformations, bond formation, synthesis planning, mechanisms, and spectroscopy and a guide to literature searching in a reader-friendly manner. Helps students understand the skills and basics they need to move from introductory to graduate organic chemistry classes Balances synthetic and physical organic chemistry in a way accessible to students Features extensive end-of-chapter problems Updates include new examples and discussion of online resources now common for literature searches Adds sections on protecting groups and green chemistry along with a rewritten chapter surveying organic spectroscopy.
(source: Nielsen Book Data)
  • Preface to the Third Edition xi Preface to the Second Edition xiii Preface to the First Edition xv 1 Reading Nomenclature 1 1.1 Acyclic Polyfunctional Molecules 2 1.2 Monocyclic Aliphatic Compounds 3 1.3 Bridged Polycyclic Structures 4 1.4 Fused Polycyclic Compounds 6 1.5 Spiro Compounds 10 1.6 Monocyclic Heterocyclic Compounds 12 1.7 Fused ]Ring Heterocyclic Compounds 14 1.8 Bridged and Spiro Heterocyclic Compounds 19 Resources 20 Problems 21 References 22 2 Accessing Chemical Information 25 2.1 Databases 25 2.2 Chemical Literature 26 2.3 Synthetic Procedures 29 2.4 Health and Safety Information 30 Problems 32 References 33 3 Stereochemistry 35 3.1 Representations 35 3.2 Vocabulary 37 3.3 Property Differences Among Stereoisomers 40 3.4 Resolution of Enantiomers 44 3.5 Enantioselective Synthesis 47 3.6 Reactions at a Stereogenic Atom 49 3.6.1 Racemization 49 3.6.2 Epimerization 50 3.6.3 Inversion 51 3.6.4 Retention 51 3.6.5 Transfer 52 3.7 Relative and Absolute Configuration 53 3.8 Topism 56 Resources 59 Problems 60 References 65 4 Mechanisms and Predictions 69 4.1 Reaction Coordinate Diagrams and Mechanisms 69 4.2 The Hammond Postulate 71 4.3 Methods for Determining Mechanisms 72 4.3.1 Identification of Products and Intermediates 72 4.3.2 Isotope Tracing 73 4.3.3 Stereochemical Determination 74 4.3.4 Concentration Dependence of Kinetics 75 4.3.5 Isotope Effects in Kinetics 85 4.3.6 Temperature Effects on Kinetics 87 4.3.7 Substituent Effects on Kinetics 90 4.4 Representative Mechanisms 95 4.4.1 Reactions in Basic Solution 96 4.4.2 Reactions in Acidic Solution 100 4.4.3 Free ]Radical Reactions 103 4.4.4 Molecular Rearrangements 106 Resources 108 Problems 109 References 120 5 Electron Delocalization, Aromatic Character, and Pericyclic Reactions 123 5.1 Molecular Orbitals 124 5.2 Aromatic Character 130 5.3 Pericyclic Reactions 135 5.3.1 Cycloaddition Reactions 137 5.3.2 Electrocyclic Reactions 142 5.3.3 Sigmatropic Reactions 147 Resources 152 Problems 152 References 158 6 Functional Group Transformations 163 6.1 Carboxylic Acids and Related Derivatives 164 6.1.1 Carboxylic Acids 164 6.1.2 Carboxylic Esters 166 6.1.3 Carboxylic Amides 168 6.1.4 Carboxylic Acid Halides 168 6.1.5 Carboxylic Anhydrides 169 6.1.6 Nitriles 169 6.1.7 O rtho Esters 170 6.2 Aldehydes, Ketones, and Derivatives 171 6.2.1 Aldehydes 171 6.2.2 Ketones 174 6.2.3 Imines and Enamines 175 6.2.4 Acetals 175 6.2.5 Vinyl Ethers 177 6.3 Alcohols 179 6.4 Ethers 179 6.5 Alkyl Halides 181 6.5.1 Alkyl Chlorides and Alkyl Bromides 182 6.5.2 Alkyl Iodides 184 6.5.3 Alkyl Fluorides 184 6.6 Amines 185 6.7 Isocyanates 187 6.8 Alkenes 187 6.9 Reductive Removal of Functionality 190 Resources 191 Problems 191 References 198 7 Carbon Carbon Bond Formation 205 7.1 Carbon Carbon Single Bond Formation 206 7.1.1 Reactions in Basic Solution 206 7.1.2 Reactions in Acidic Solution 214 7.1.3 O rganometallic Coupling Reactions 217 7.2 Carbon Carbon Double ]Bond Formation 218 7.3 Multibond Processes 222 Resources 224 Problems 224 References 230 8 Planning Multistep Syntheses 235 8.1 Retrosynthetic Analysis 235 8.2 Disconnection at a Functional Group or Branch Point 236 8.3 Cooperation for Difunctionality 244 8.4 Ring Closure 250 8.5 Acetylide Alkylation and Addition 253 8.6 T he Diels Alder Reaction 255 8.7 T he Claisen Rearrangement 259 8.8 Synthetic Strategies 263 8.9 Final Note 265 Resources 266 Problems 266 References 271 9 Physical Influences on Reactions 277 9.1 Unimolecular Reactions 278 9.2 Homogenous Two ]Component Reactions 279 9.3 Temperature Effects 280 9.4 Pressure Effects 281 9.5 Solvent Effects 282 9.6 Biphasic Reactions 283 9.6.1 Phase Transfer Catalysis 283 9.6.2 Increasing Solubility 286 9.6.3 Increasing Surface Area 287 9.6.4 Ultrasound 287 9.7 Reactions on Chemical Supports 288 9.8 Using Unfavorable Equilibria 291 9.9 Green Chemistry 293 Resources 294 Problems 294 References 295 10 Survey of Organic Spectroscopy 299 10.1 Electromagnetic Radiation 299 10.2 Ultraviolet Spectroscopy 300 10.2.1 Origin of the Signals 300 10.2.2 Interpretation 302 10.2.3 Visible Spectroscopy 302 10.3 Infrared Spectroscopy 303 10.3.1 Origin of the Signals 304 10.3.2 Interpretation 304 10.4 Mass Spectrometry 305 10.4.1 Origin of the Signals 306 10.4.2 Interpretation 307 10.5 N MR Spectroscopy 309 10.5.1 Origin of the Signals 309 10.5.2 Interpretation of Proton NMR Spectra 311 10.6 Carbon NMR Spectra 323 10.6.1 General Characteristics 323 10.6.2 Interpretation of 13C NMR Spectra 325 10.7 Correlation of 1H and 13C NMR Spectra 327 Resources 329 Problems 329 References 333 Appendix A 337 Appendix B 341 Index 347.
  • (source: Nielsen Book Data)
This book presents key aspects of organic synthesis stereochemistry, functional group transformations, bond formation, synthesis planning, mechanisms, and spectroscopy and a guide to literature searching in a reader-friendly manner. Helps students understand the skills and basics they need to move from introductory to graduate organic chemistry classes Balances synthetic and physical organic chemistry in a way accessible to students Features extensive end-of-chapter problems Updates include new examples and discussion of online resources now common for literature searches Adds sections on protecting groups and green chemistry along with a rewritten chapter surveying organic spectroscopy.
(source: Nielsen Book Data)
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD251.2 .S75 2016 Unknown
Book
xiii, 300 pages : illustrations ; 23 cm
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD261 .Z83 2016 Unavailable On order Request

4. Organic chemistry [2016]

Book
xxx, 1054, 59, 34 pages : illustrations ; 26 cm
  • 1. Structure and Bonding. 2. Polar Covalent Bonds-- Acids and Bases. 3. Organic Compounds: Alkanes and Their Stereochemistry. 4. Organic Compounds: Cycloalkanes and Their Stereochemistry 5. Stereochemistry at Tetrahedral Centers. 6. An Overview of Organic Reactions. 7. Alkenes: Structure and Reactivity. Practice Your Scientific Analysis and Reasoning I: The Chiral Drug Thalidomide 8. Alkenes: Reactions and Synthesis. 9. Alkynes: An Introduction to Organic Synthesis. 10. Organohalides. 11. Reactions of Alkyl Halides: Nucleophilic Substitutions and Eliminations. Practice Your Scientific Analysis and Reasoning II: From Mustard Gas to Alkylating Anticancer Drugs 12. Structure Determination: Mass Spectrometry and Infrared Spectroscopy. 13. Structure Determination: Nuclear Magnetic Resonance Spectroscopy. 14. Conjugated Compounds and Ultraviolet Spectroscopy. 15. Benzene and Aromaticity. Practice Your Scientific Analysis and Reasoning III: Photodynamic Therapy (PDT) 16. Chemistry of Benzene: Electrophilic Aromatic Substitution. 17. Alcohols and Phenols. 18. Ethers and Epoxides-- Thiols and Sulfides. Preview of Carbonyl Chemistry. 19. Aldehydes and Ketones: Nucleophilic Addition Reactions. Practice Your Scientific Analysis and Reasoning IV: SSRIs 20. Carboxylic Acids and Nitriles. 21. Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions. 22. Carbonyl Alpha-Substitution Reactions. 23. Carbonyl Condensation Reactions. Practice Your Scientific Analysis and Reasoning V: Thymine in DNA 24. Amines and Heterocycles. 25. Biomolecules: Carbohydrates. 26. Biomolecules: Amino Acids, Peptides, and Proteins. Practice Your Scientific Analysis and Reasoning VI: Melatonin and Serotonin 27. Biomolecules: Lipids. 28. Biomolecules: Nucleic Acids. 29. The Organic Chemistry of Metabolic Pathways. 30. Orbitals and Organic Chemistry: Pericyclic Reactions. 31. Synthetic Polymers. Practice Your Scientific Analysis and Reasoning VII: The Potent Antibiotic of Endiandric Acid C.
  • (source: Nielsen Book Data)
Master organic chemistry with the help of this proven best-seller! John McMurry's Organic Chemistry is consistently praised as the most clearly written book available for the course. In John McMurry's words: "I wrote this book because I love writing. I get great pleasure and satisfaction from taking a complicated subject, turning it around until I see it clearly from a new angle, and then explaining it in simple words." Through his lucid writing and ability to show the beauty and logic of organic chemistry, McMurry makes learning enjoyable. The highest compliment that can be given to a chemistry book applies to McMurry: It works!.
(source: Nielsen Book Data)
  • 1. Structure and Bonding. 2. Polar Covalent Bonds-- Acids and Bases. 3. Organic Compounds: Alkanes and Their Stereochemistry. 4. Organic Compounds: Cycloalkanes and Their Stereochemistry 5. Stereochemistry at Tetrahedral Centers. 6. An Overview of Organic Reactions. 7. Alkenes: Structure and Reactivity. Practice Your Scientific Analysis and Reasoning I: The Chiral Drug Thalidomide 8. Alkenes: Reactions and Synthesis. 9. Alkynes: An Introduction to Organic Synthesis. 10. Organohalides. 11. Reactions of Alkyl Halides: Nucleophilic Substitutions and Eliminations. Practice Your Scientific Analysis and Reasoning II: From Mustard Gas to Alkylating Anticancer Drugs 12. Structure Determination: Mass Spectrometry and Infrared Spectroscopy. 13. Structure Determination: Nuclear Magnetic Resonance Spectroscopy. 14. Conjugated Compounds and Ultraviolet Spectroscopy. 15. Benzene and Aromaticity. Practice Your Scientific Analysis and Reasoning III: Photodynamic Therapy (PDT) 16. Chemistry of Benzene: Electrophilic Aromatic Substitution. 17. Alcohols and Phenols. 18. Ethers and Epoxides-- Thiols and Sulfides. Preview of Carbonyl Chemistry. 19. Aldehydes and Ketones: Nucleophilic Addition Reactions. Practice Your Scientific Analysis and Reasoning IV: SSRIs 20. Carboxylic Acids and Nitriles. 21. Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions. 22. Carbonyl Alpha-Substitution Reactions. 23. Carbonyl Condensation Reactions. Practice Your Scientific Analysis and Reasoning V: Thymine in DNA 24. Amines and Heterocycles. 25. Biomolecules: Carbohydrates. 26. Biomolecules: Amino Acids, Peptides, and Proteins. Practice Your Scientific Analysis and Reasoning VI: Melatonin and Serotonin 27. Biomolecules: Lipids. 28. Biomolecules: Nucleic Acids. 29. The Organic Chemistry of Metabolic Pathways. 30. Orbitals and Organic Chemistry: Pericyclic Reactions. 31. Synthetic Polymers. Practice Your Scientific Analysis and Reasoning VII: The Potent Antibiotic of Endiandric Acid C.
  • (source: Nielsen Book Data)
Master organic chemistry with the help of this proven best-seller! John McMurry's Organic Chemistry is consistently praised as the most clearly written book available for the course. In John McMurry's words: "I wrote this book because I love writing. I get great pleasure and satisfaction from taking a complicated subject, turning it around until I see it clearly from a new angle, and then explaining it in simple words." Through his lucid writing and ability to show the beauty and logic of organic chemistry, McMurry makes learning enjoyable. The highest compliment that can be given to a chemistry book applies to McMurry: It works!.
(source: Nielsen Book Data)
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
On reserve: Ask at circulation desk
QD251.3 .M364 2016 Unknown On Reserve 2-hour loan
QD251.3 .M364 2016 Unknown On Reserve 2-hour loan
CHEM-131-01, CHEM-131-01
Course
CHEM-131-01 -- Organic Polyfunctional Compounds
Instructor(s)
Kool, Eric Todd
Course
CHEM-131-01 -- Organic Polyfunctional Compounds
Instructor(s)
Xia, Yan
Book
vii, 387 pages : illustrations ; 24 cm
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
On reserve: Ask at circulation desk
QD256 .K54 2016 Unknown On Reserve 2-hour loan
CHEM-33-01, CHEM-33-01, CHEM-33-01
Course
CHEM-33-01 -- Structure and Reactivity
Instructor(s)
Kanan, Matthew W.
Course
CHEM-33-01 -- Structure and Reactivity
Instructor(s)
McClory, Megan Kathleen
Course
CHEM-33-01 -- Structure and Reactivity
Instructor(s)
Wender, Paul A
Book
xxiv, 763, I-13 : illustrations ; 24 cm
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD411 .S65 2016 Unknown
Book
xxii, 1012 pages : illustrations ; 29 cm.
  • Introduction. WELCOME TO ORGANIC CHEMISTRY. Laboratory Safety. Organization of the Textbook. Advance Preparation. Budgeting Time. Purpose. PART I: INTRODUCTION TO BASIC LABORATORY TECHNIQUES. Experiment 1. Solubility. Experiment 2. Crystallization. Experiment 3. Extraction. Experiment 4. A Separation and Purification Scheme. Experiment 4A. Extractions with a Separatory Funnel. Experiment 4B. Extractions with a Screw-Cap Centrifuge Tube Experiment 5. Chromatography. Experiment 5A. Thin-Layer Chromatography. Experiment 5B. Selecting the Correct Solvent for Thin-Layer Chromatography. Experiment 5C. Monitoring a Reaction with Thin Layer Chromatography. Experiment 5D. Column Chromatography. Experiment 6. Simple and Fractional Distillation Experiment 7. Infrared Spectroscopy and Boiling-Point Determination Essay. Aspirin. Experiment 8. Acetylsalicylic Acid. Essay. Analgesics. Experiment 9. Acetaminophen. Essay. Identification of Drugs. Experiment 10.TLC Analysis of Analgesic Drugs. Essay. Caffeine. Experiment 11. Isolation of Caffeine. Experiment 11A. Extraction of Caffeine from Tea. Experiment 11B. Isolation of Caffeine from a Tea Bag. Essay. Esters--Flavors and Fragrances. Experiment 12: Isopentyl Acetate (Banana Oil). Essay, Terpenes and Phenylpropanoids. Experiment 13. Isolation of Eugenol from Cloves. Essay. Stereochemical Theory of Odor. Experiment 14. Spearmint and Caraway Oil: (+)- and (-)- Carvones. Essay.The Chemistry of Vision. Experiment 15. Isolation of Chlorophyll and Carotenoid Pigments from Spinach. Essay: Ethanol and Fermentation Chemistry. Experiment 16. Ethanol from Sucrose. PART II: INTRODUCTION TO MOLECULAR MODELING. Essay: Molecular Modeling and Molecular Mechanics. Experiment 17. An Introduction to Molecular Modeling. Experiment 17A. The Conformations of n-Butane: Local Minima. Experiment 17B. Cyclohexane Chair and Boat Conformations. Experiment 17C. Substituted Cyclohexane Rings (Critical Thinking Exercise). Experiment 17D. cis- and trans-2-Butene. Essay: Computational Chemistry - Ab initio and Semiempirical Methods. Experiment 18. Computational Chemistry. Experiment 18A. Heats of Formation: Isomerism, Tautomerism, and Regioselectivity. Experiment 18B. Heats of Reactions: SN1 Reaction Rates. Experiment 18C. Density-Electrostatic Potential. Maps: Acidities of Carboxylic Acids. Experiment 18D. Density -Electrostatic Potential Maps: Carbocations. Experiment 18E. Density -LUMO Maps: Reactivities of Carbonyl Groups. PART III: PREPARATIONS AND REACTIONS OF ORGANIC COMPOUNDS. Experiment 19. Reactivities of Some Alkyl Halides. Experiment 20. Nucleophilic Substitution Reactions: Competing Nucleophiles Experiment 20A. Competing Nucleophiles with 1-Butanol or 2-Butanol. Experiment 20B. Competing Nucleophiles with 2-Methyl-2-Propanol. Experiment 20C. Analysis. Experiment 21. Synthesis of n-Butyl Bromide and t-Pentyl Chloride. Experiment 21A. n-Butyl Bromide. Experiment 21B. t-Pentyl Chloride. Experiment 22. 4-Methylcyclohexen Essay. Fats and Oils. Experiment 23. Methyl Stearate from Methyl Oleate. Essay: Soap Experiment 24. Preparation of Soap. Essay: Petroleum and Fossil Fuels. Experiment 25. Gas Chromatographic Analysis of Gasolines. Essay: Biofuels. Experiment 26. Biodiesel. Experiment 26A. Biodiesel from Coconut Oil. Experiment 26B. Biodiesel from Other Oils. Experiment 26C. Analysis of Biodiesel. Essay: Green Chemistry. Experiment 27. Chiral Reduction of Ethyl Acetoacetate-- Optical Purity Determination. Experiment 27A. Chiral Reduction of Ethyl Acetoacetate. Experiment 27B. NMR Determination of the Optical Purity of Ethyl (S)-3-Hydroxybutanoate. Experiment 28. Nitration of Aromatic Compounds Using a Recyclable Catalyst. Experiment 29. Reduction of Ketones Using Carrots as Biological Reducing Agents Experiment 30. Resolution of (+/-)-alpha-Phenylethylamine and Determination of Optical Purity. Experiment 30A. Resolution of (+/-)-alpha-Phenylethylamine. Experiment 30B. Determination of Optical Purity Using NMR and a Chiral Resolving Agent. Experiment 31. An Oxidation-Reduction Scheme: Borneol, Camphor, Isoborneol. Experiment 32. Multistep Reaction Sequences: The Conversion of Benzaldehyde to Benzilic Acid. Experiment 32A. Preparation of Benzoin by Thiamine Catalysis. Experiment 32B. Preparation of Benzil. Experiment 32C. Preparation of Benzilic Acid. Experiment 33. Triphenylmethanol and Benzoic Acid. Experiment 33A. Triphenylmethanol. Experiment 33B. Benzoic Acid. Experiment 34. Aqueous-Based Organozinc Reactions. Experiment 35. Sonogashira Coupling of Iodosubstituted Aromatic Compounds with Alkynes Using a Palladium Catalyst. Experiment 36. Grubbs Catalyzed Metathesis of Eugenol with 1,4-Butenediol to Prepare a Natural Product. Experiment 37. The Aldol Condensation Reaction: Preparation of Benzalacetophenones (Chalcones). Experiment 38. A Green Enantioselective Aldol Condensation Reaction. Experiment 39. Preparation of an ?, ?-Unsaturated Ketone via Michael and Aldol Condensation Reactions. Experiment 40. Preparation of Triphenylpyridine. Experiment 41. 1,4-Diphenyl-1,3-Butadiene. Experiment 42. Relative Reactivities of Several Aromatic Compounds. Experiment 43. Nitration of Methyl Benzoate. Essay: Synthetic Dyes. Experiment 44. Preparation of Methyl Orange. Experiment 45. Preparation of Indigo. Experiment 46. Formulation of a Paint and Art Project. Essay. Local Anesthetics. Experiment 47. Benzocaine. Essay. Pheromones: Insect Attractants and Repellants. Experiment 48. N, N-Diethyl-m-toluamide: The Insect Repellent "OFF." Essay: Sulfa Drugs. Experiment 49. Sulfa Drugs: Preparation of Sulfanilamide. Essay: Polymers and Plastics. Experiment 50. Preparation and Properties of Polymers: Polyester, Nylon, and Polystyrene. Experiment 50A. Polyesters. Experiment 50B. Polyamide (Nylon). Experiment 50C. Polystyrene. Experiment 50D. Infrared Spectra of Polymer Samples. Experiment 51. Ring-Opening Metathesis Polymerization (ROMP) Using a Grubbs Catalyst: A Three Step Synthesis of a Polymer. Experiment 51A. Diels-Adler Reaction. Experiment 51B. Conversion of the Diels-Adler Adduct to the Diester. Experiment 51C. Synthesizing the Polymer by Ring-Opening Metathesis Polymerization ROMP) Essay. Diels-Alder Reaction and Insecticides. Experiment 52. The Diels-Alder Reaction of Cyclopentadiene with Maleic Anhydride. Experiment 53. Diels-Adler Reaction with Anthracine-9-Methanol. Experiment 54. Photoreduction of Benzophenone and Rearrangement of Benzpinacol to Benzopinacolone. Experiment 54A. Photoreduction of Benzophenone. Experiment 54B. Synthesis of ?-Benzopinacolone: The Acid-Catalyzed Rearrangement of Benzpinacol. Essay. Fireflies and Photochemistry. Experiment 55. Luminol. Essay. The Chemistry of Sweeteners. Experiment 56. Carbohydrates. Experiment 57. Analysis of a Diet Soft Drink by HPLC. Part IV: IDENTIFICATION OF ORGANIC SUBSTANCES. Experiment 58. Identification of Unknowns. Experiment 58A. Solubility Tests. Experiment 58B. Tests for the Elements (N, S, X). Experiment 58C. Tests for Unsaturation. Experiment 58D. Aldehydes and Ketones. Experiment 58E. Carboxylic Acids. Experiment 58F. Phenols. Experiment 58G. Amines. Experiment 58H. Alcohols. Experiment 58I. Esters. PART V: PROJECT-BASED EXPERIMENTS. Experiment 59. Preparation of a C-4 or C-5 Acetate Ester. Experiment 60. Competing Nucleophiles in SN1 and SN2 Reactions: Investigations Using 2-Pentanol and 3-Pentanol. Experiment 61. Friedel-Crafts Acylation. Experiment 62. The Analysis of Antihistamine Drugs by Gas Chromatography-Mass Spectrometry. Experiment 63. Carbonation of an Unknown Aromatic Halide. Experiment 64. The Aldehyde Enigma. Experiment 65. Synthesis of Substituted Chalcones: A Guided-Inquiry Experience. Experiment 66. Green Epoxidation of Chalcones. Experiment 67. Cyclopropanation Reactions of Chalcones. Experiment 68. Michael and Aldol Condensation Reactions. Experiment 69. Esterification Reactions of Vanillin: The Use of NMR to Determine a Structure. PART VI: THE TECHNIQUES. Technique 1. Laboratory Safety. Technique 2. The Laboratory Notebook, Calculations, and Laboratory Records. Technique 3. Laboratory Glassware: Care and Cleaning. Technique 4. How to Find Data for Compounds: Handbooks and Catalogues. Technique 5. Measurement of Volume and Weight. Technique 6. Heating and Cooling Methods. Technique 7. Reaction Methods. Technique 8. Filtration. Technique 9. Physical Constants of Solids: The Melting Point. Technique 10. Solubility. Technique 11. Crystallization: Purification of Solids. Technique 12. Extractions, Separations, and Drying Agents. Technique 13. Physical Constants of Liquids: The Boiling Point and Density. Technique 14. Simple Distillation. Technique 15. Fractional Distillation, Azeotropes. Technique 16. Vacuum Distillation, Manometers. Technique 17. Sublimation. Technique 18. Steam Distillation. Technique 19. Column Chromatography. Technique 20. Thin-Layer Chromatography. Technique 21. High-Performance Liquid Chromatography (HPLC). Technique 22. Gas Chromatography. Technique 23. Polarimetry. Technique 24. Refractometry. Technique 25. Infrared Spectroscopy. Technique 26. Nuclear Magnetic Resonance Spectroscopy (Proton NMR). Technique 27. Carbon-13 Nuclear Magnetic Resonance Spectroscopy. Technique 28. Mass Spectrometry. Technique 29. Guide to the Chemical Literature Appendix 1: Tables of Unknowns and Derivatives. Appendix 2: Procedure for Preparing Derivatives. Appendix 3: Index of Spectra.
  • (source: Nielsen Book Data)
Featuring new experiments, a new essay, and new coverage of nanotechnology, this organic chemistry laboratory textbook offers a comprehensive treatment of laboratory techniques including small scale and some microscale methods that use standard-scale ("macroscale") glassware and equipment. The book is organized based on essays and topics of current interest and covers a large number of traditional organic reactions and syntheses, as well as experiments with a biological or health science focus. Seven introductory technique-based experiments, thirteen project-based experiments, and sections on green chemistry and biofuels spark students' interest and engage them in the learning process. Instructors may choose to offer Cengage Learning's optional Premium Website, which contains videos on basic organic laboratory techniques.
(source: Nielsen Book Data)
  • Introduction. WELCOME TO ORGANIC CHEMISTRY. Laboratory Safety. Organization of the Textbook. Advance Preparation. Budgeting Time. Purpose. PART I: INTRODUCTION TO BASIC LABORATORY TECHNIQUES. Experiment 1. Solubility. Experiment 2. Crystallization. Experiment 3. Extraction. Experiment 4. A Separation and Purification Scheme. Experiment 4A. Extractions with a Separatory Funnel. Experiment 4B. Extractions with a Screw-Cap Centrifuge Tube Experiment 5. Chromatography. Experiment 5A. Thin-Layer Chromatography. Experiment 5B. Selecting the Correct Solvent for Thin-Layer Chromatography. Experiment 5C. Monitoring a Reaction with Thin Layer Chromatography. Experiment 5D. Column Chromatography. Experiment 6. Simple and Fractional Distillation Experiment 7. Infrared Spectroscopy and Boiling-Point Determination Essay. Aspirin. Experiment 8. Acetylsalicylic Acid. Essay. Analgesics. Experiment 9. Acetaminophen. Essay. Identification of Drugs. Experiment 10.TLC Analysis of Analgesic Drugs. Essay. Caffeine. Experiment 11. Isolation of Caffeine. Experiment 11A. Extraction of Caffeine from Tea. Experiment 11B. Isolation of Caffeine from a Tea Bag. Essay. Esters--Flavors and Fragrances. Experiment 12: Isopentyl Acetate (Banana Oil). Essay, Terpenes and Phenylpropanoids. Experiment 13. Isolation of Eugenol from Cloves. Essay. Stereochemical Theory of Odor. Experiment 14. Spearmint and Caraway Oil: (+)- and (-)- Carvones. Essay.The Chemistry of Vision. Experiment 15. Isolation of Chlorophyll and Carotenoid Pigments from Spinach. Essay: Ethanol and Fermentation Chemistry. Experiment 16. Ethanol from Sucrose. PART II: INTRODUCTION TO MOLECULAR MODELING. Essay: Molecular Modeling and Molecular Mechanics. Experiment 17. An Introduction to Molecular Modeling. Experiment 17A. The Conformations of n-Butane: Local Minima. Experiment 17B. Cyclohexane Chair and Boat Conformations. Experiment 17C. Substituted Cyclohexane Rings (Critical Thinking Exercise). Experiment 17D. cis- and trans-2-Butene. Essay: Computational Chemistry - Ab initio and Semiempirical Methods. Experiment 18. Computational Chemistry. Experiment 18A. Heats of Formation: Isomerism, Tautomerism, and Regioselectivity. Experiment 18B. Heats of Reactions: SN1 Reaction Rates. Experiment 18C. Density-Electrostatic Potential. Maps: Acidities of Carboxylic Acids. Experiment 18D. Density -Electrostatic Potential Maps: Carbocations. Experiment 18E. Density -LUMO Maps: Reactivities of Carbonyl Groups. PART III: PREPARATIONS AND REACTIONS OF ORGANIC COMPOUNDS. Experiment 19. Reactivities of Some Alkyl Halides. Experiment 20. Nucleophilic Substitution Reactions: Competing Nucleophiles Experiment 20A. Competing Nucleophiles with 1-Butanol or 2-Butanol. Experiment 20B. Competing Nucleophiles with 2-Methyl-2-Propanol. Experiment 20C. Analysis. Experiment 21. Synthesis of n-Butyl Bromide and t-Pentyl Chloride. Experiment 21A. n-Butyl Bromide. Experiment 21B. t-Pentyl Chloride. Experiment 22. 4-Methylcyclohexen Essay. Fats and Oils. Experiment 23. Methyl Stearate from Methyl Oleate. Essay: Soap Experiment 24. Preparation of Soap. Essay: Petroleum and Fossil Fuels. Experiment 25. Gas Chromatographic Analysis of Gasolines. Essay: Biofuels. Experiment 26. Biodiesel. Experiment 26A. Biodiesel from Coconut Oil. Experiment 26B. Biodiesel from Other Oils. Experiment 26C. Analysis of Biodiesel. Essay: Green Chemistry. Experiment 27. Chiral Reduction of Ethyl Acetoacetate-- Optical Purity Determination. Experiment 27A. Chiral Reduction of Ethyl Acetoacetate. Experiment 27B. NMR Determination of the Optical Purity of Ethyl (S)-3-Hydroxybutanoate. Experiment 28. Nitration of Aromatic Compounds Using a Recyclable Catalyst. Experiment 29. Reduction of Ketones Using Carrots as Biological Reducing Agents Experiment 30. Resolution of (+/-)-alpha-Phenylethylamine and Determination of Optical Purity. Experiment 30A. Resolution of (+/-)-alpha-Phenylethylamine. Experiment 30B. Determination of Optical Purity Using NMR and a Chiral Resolving Agent. Experiment 31. An Oxidation-Reduction Scheme: Borneol, Camphor, Isoborneol. Experiment 32. Multistep Reaction Sequences: The Conversion of Benzaldehyde to Benzilic Acid. Experiment 32A. Preparation of Benzoin by Thiamine Catalysis. Experiment 32B. Preparation of Benzil. Experiment 32C. Preparation of Benzilic Acid. Experiment 33. Triphenylmethanol and Benzoic Acid. Experiment 33A. Triphenylmethanol. Experiment 33B. Benzoic Acid. Experiment 34. Aqueous-Based Organozinc Reactions. Experiment 35. Sonogashira Coupling of Iodosubstituted Aromatic Compounds with Alkynes Using a Palladium Catalyst. Experiment 36. Grubbs Catalyzed Metathesis of Eugenol with 1,4-Butenediol to Prepare a Natural Product. Experiment 37. The Aldol Condensation Reaction: Preparation of Benzalacetophenones (Chalcones). Experiment 38. A Green Enantioselective Aldol Condensation Reaction. Experiment 39. Preparation of an ?, ?-Unsaturated Ketone via Michael and Aldol Condensation Reactions. Experiment 40. Preparation of Triphenylpyridine. Experiment 41. 1,4-Diphenyl-1,3-Butadiene. Experiment 42. Relative Reactivities of Several Aromatic Compounds. Experiment 43. Nitration of Methyl Benzoate. Essay: Synthetic Dyes. Experiment 44. Preparation of Methyl Orange. Experiment 45. Preparation of Indigo. Experiment 46. Formulation of a Paint and Art Project. Essay. Local Anesthetics. Experiment 47. Benzocaine. Essay. Pheromones: Insect Attractants and Repellants. Experiment 48. N, N-Diethyl-m-toluamide: The Insect Repellent "OFF." Essay: Sulfa Drugs. Experiment 49. Sulfa Drugs: Preparation of Sulfanilamide. Essay: Polymers and Plastics. Experiment 50. Preparation and Properties of Polymers: Polyester, Nylon, and Polystyrene. Experiment 50A. Polyesters. Experiment 50B. Polyamide (Nylon). Experiment 50C. Polystyrene. Experiment 50D. Infrared Spectra of Polymer Samples. Experiment 51. Ring-Opening Metathesis Polymerization (ROMP) Using a Grubbs Catalyst: A Three Step Synthesis of a Polymer. Experiment 51A. Diels-Adler Reaction. Experiment 51B. Conversion of the Diels-Adler Adduct to the Diester. Experiment 51C. Synthesizing the Polymer by Ring-Opening Metathesis Polymerization ROMP) Essay. Diels-Alder Reaction and Insecticides. Experiment 52. The Diels-Alder Reaction of Cyclopentadiene with Maleic Anhydride. Experiment 53. Diels-Adler Reaction with Anthracine-9-Methanol. Experiment 54. Photoreduction of Benzophenone and Rearrangement of Benzpinacol to Benzopinacolone. Experiment 54A. Photoreduction of Benzophenone. Experiment 54B. Synthesis of ?-Benzopinacolone: The Acid-Catalyzed Rearrangement of Benzpinacol. Essay. Fireflies and Photochemistry. Experiment 55. Luminol. Essay. The Chemistry of Sweeteners. Experiment 56. Carbohydrates. Experiment 57. Analysis of a Diet Soft Drink by HPLC. Part IV: IDENTIFICATION OF ORGANIC SUBSTANCES. Experiment 58. Identification of Unknowns. Experiment 58A. Solubility Tests. Experiment 58B. Tests for the Elements (N, S, X). Experiment 58C. Tests for Unsaturation. Experiment 58D. Aldehydes and Ketones. Experiment 58E. Carboxylic Acids. Experiment 58F. Phenols. Experiment 58G. Amines. Experiment 58H. Alcohols. Experiment 58I. Esters. PART V: PROJECT-BASED EXPERIMENTS. Experiment 59. Preparation of a C-4 or C-5 Acetate Ester. Experiment 60. Competing Nucleophiles in SN1 and SN2 Reactions: Investigations Using 2-Pentanol and 3-Pentanol. Experiment 61. Friedel-Crafts Acylation. Experiment 62. The Analysis of Antihistamine Drugs by Gas Chromatography-Mass Spectrometry. Experiment 63. Carbonation of an Unknown Aromatic Halide. Experiment 64. The Aldehyde Enigma. Experiment 65. Synthesis of Substituted Chalcones: A Guided-Inquiry Experience. Experiment 66. Green Epoxidation of Chalcones. Experiment 67. Cyclopropanation Reactions of Chalcones. Experiment 68. Michael and Aldol Condensation Reactions. Experiment 69. Esterification Reactions of Vanillin: The Use of NMR to Determine a Structure. PART VI: THE TECHNIQUES. Technique 1. Laboratory Safety. Technique 2. The Laboratory Notebook, Calculations, and Laboratory Records. Technique 3. Laboratory Glassware: Care and Cleaning. Technique 4. How to Find Data for Compounds: Handbooks and Catalogues. Technique 5. Measurement of Volume and Weight. Technique 6. Heating and Cooling Methods. Technique 7. Reaction Methods. Technique 8. Filtration. Technique 9. Physical Constants of Solids: The Melting Point. Technique 10. Solubility. Technique 11. Crystallization: Purification of Solids. Technique 12. Extractions, Separations, and Drying Agents. Technique 13. Physical Constants of Liquids: The Boiling Point and Density. Technique 14. Simple Distillation. Technique 15. Fractional Distillation, Azeotropes. Technique 16. Vacuum Distillation, Manometers. Technique 17. Sublimation. Technique 18. Steam Distillation. Technique 19. Column Chromatography. Technique 20. Thin-Layer Chromatography. Technique 21. High-Performance Liquid Chromatography (HPLC). Technique 22. Gas Chromatography. Technique 23. Polarimetry. Technique 24. Refractometry. Technique 25. Infrared Spectroscopy. Technique 26. Nuclear Magnetic Resonance Spectroscopy (Proton NMR). Technique 27. Carbon-13 Nuclear Magnetic Resonance Spectroscopy. Technique 28. Mass Spectrometry. Technique 29. Guide to the Chemical Literature Appendix 1: Tables of Unknowns and Derivatives. Appendix 2: Procedure for Preparing Derivatives. Appendix 3: Index of Spectra.
  • (source: Nielsen Book Data)
Featuring new experiments, a new essay, and new coverage of nanotechnology, this organic chemistry laboratory textbook offers a comprehensive treatment of laboratory techniques including small scale and some microscale methods that use standard-scale ("macroscale") glassware and equipment. The book is organized based on essays and topics of current interest and covers a large number of traditional organic reactions and syntheses, as well as experiments with a biological or health science focus. Seven introductory technique-based experiments, thirteen project-based experiments, and sections on green chemistry and biofuels spark students' interest and engage them in the learning process. Instructors may choose to offer Cengage Learning's optional Premium Website, which contains videos on basic organic laboratory techniques.
(source: Nielsen Book Data)
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD261 .I543 2016 Unknown
Book
vi, 1116, [1] pages : illustrations ; 28 cm
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
On reserve: Ask at circulation desk
QD251.3 .M3642 2016 Unknown On Reserve 2-hour loan
QD251.3 .M3642 2016 Unknown On Reserve 2-hour loan
CHEM-131-01, CHEM-131-01
Course
CHEM-131-01 -- Organic Polyfunctional Compounds
Instructor(s)
Kool, Eric Todd
Course
CHEM-131-01 -- Organic Polyfunctional Compounds
Instructor(s)
Xia, Yan
Book
vii, 264 pages : illustrations ; 23 cm.
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD257 .M66 2015 Unavailable At bindery Request
Book
xi, 315 pages : illustrations ; 24 cm
  • Introduction Marion H. Emmert Radical-Mediated C-H Bond Activation Adam M. Azman Pd-Catalyzed C-H Functionalization Jesse D. Carrick Rhodium-Catalyzed C-H Activation Micheal Fultz Nickel-Catalyzed C-H Activation Andrew C. Williams Iron-Catalyzed C-H Activation Narendra B. Ambhaikar Copper-Mediated C-H Activation Nadia M. Ahmad Cobalt-Catalyzed C-H Activation Eric J. Medici and Nicole L. Snyder Fluorination and Trifluoromethylation of Arenes and Heteroarenes via C-H Activation Ji Zhang and Timothy T. Curran C-H Activation of Heteroaromatics Donna A. A. Wilton.
  • (source: Nielsen Book Data)
Greener than conventional methods, C-H activation methods have flourished during the last decade and become especially attractive to organic chemists. Edited by a practioner in this rapidly developing field, C-H Bond Activation in Organic Synthesis provides an overview of this exciting playground of chemistry. The book summarizes the state of the art in C-H activation for functionalization, enabling you to carry out reactions in the most environmentally friendly fashion with the least contamination of by-products. The most popular C-H activation reactions are catalyzed by transition metals. This book dedicates a chapter to each of the following catalysts: palladium, rhodium, nickel, iron, copper, and cobalt. In addition, it covers radical-mediated C-H activation, fluorination via C-H activation, and C-H activation of heterocycles. Using a pedagogically practical approach, each chapter is divided by the transition metal catalyst, not a specific transformation. This gives you an up-to-date review of the most important topics of C-H activation. The area of C-H activation has experienced a flurry of activity over the past two decades, so the time is right for a resource that summarizes these powerful tools with which you can design and construct heteroaromatic molecules. Thus, direct C-H functionalization methods are expected to continue to greatly contribute to the mission of green chemistry: low-energy, waste-free, and atom-economic transformations for the synthesis of organic materials and biologically active molecules in the twenty-first century. Using this book, you can carry out environmentally friendly reactions that enable the conversion of cheap and abundant alkanes into valuable functionalized organic compounds.
(source: Nielsen Book Data)
  • Introduction Marion H. Emmert Radical-Mediated C-H Bond Activation Adam M. Azman Pd-Catalyzed C-H Functionalization Jesse D. Carrick Rhodium-Catalyzed C-H Activation Micheal Fultz Nickel-Catalyzed C-H Activation Andrew C. Williams Iron-Catalyzed C-H Activation Narendra B. Ambhaikar Copper-Mediated C-H Activation Nadia M. Ahmad Cobalt-Catalyzed C-H Activation Eric J. Medici and Nicole L. Snyder Fluorination and Trifluoromethylation of Arenes and Heteroarenes via C-H Activation Ji Zhang and Timothy T. Curran C-H Activation of Heteroaromatics Donna A. A. Wilton.
  • (source: Nielsen Book Data)
Greener than conventional methods, C-H activation methods have flourished during the last decade and become especially attractive to organic chemists. Edited by a practioner in this rapidly developing field, C-H Bond Activation in Organic Synthesis provides an overview of this exciting playground of chemistry. The book summarizes the state of the art in C-H activation for functionalization, enabling you to carry out reactions in the most environmentally friendly fashion with the least contamination of by-products. The most popular C-H activation reactions are catalyzed by transition metals. This book dedicates a chapter to each of the following catalysts: palladium, rhodium, nickel, iron, copper, and cobalt. In addition, it covers radical-mediated C-H activation, fluorination via C-H activation, and C-H activation of heterocycles. Using a pedagogically practical approach, each chapter is divided by the transition metal catalyst, not a specific transformation. This gives you an up-to-date review of the most important topics of C-H activation. The area of C-H activation has experienced a flurry of activity over the past two decades, so the time is right for a resource that summarizes these powerful tools with which you can design and construct heteroaromatic molecules. Thus, direct C-H functionalization methods are expected to continue to greatly contribute to the mission of green chemistry: low-energy, waste-free, and atom-economic transformations for the synthesis of organic materials and biologically active molecules in the twenty-first century. Using this book, you can carry out environmentally friendly reactions that enable the conversion of cheap and abundant alkanes into valuable functionalized organic compounds.
(source: Nielsen Book Data)
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD271 .C27 2015 Unknown
Book
xvi, 381 pages : illustrations ; 25 cm
  • Introduction Synthesis of Pyrroles and N-Vinylpyrroles by the Reaction of Ketones (Ketoximes) with Acetylenes Heterocyclization of ketoximes with acetylene Regioselectivity of the reaction Substituted acetylenes in reactions with ketoximes Vinyl halogenides and dihalogenethanes as synthetic equivalents of acetylene Intermediate stages and side reactions delta-Carbolines from 3-acylindoles and acetylene Reaction of ketoximes with acetylene in the presence of ketones. One-pot assembly of 4-methylen-3-oxa-1-azabicyclo[3.1.0]hexanes Transformations of aldoximes in the systems MOH/DMSO and MOH/DMSO/acetylene Mechanism of pyrrole synthesis from ketoximes and acetylene Novel Aspects of NH- and N-Vinylpyrroles Reactivity Reaction with the participation of the pyrrole ring Reactions with participation of the vinyl group Conclusions References Index.
  • (source: Nielsen Book Data)
During the last 30 years, knowledge of the essential role that pyrrole structures play in the chemistry of living organisms, drug design, and the development of advanced materials has increased. Correspondingly, research on the diverse issues of synthetic, theoretical, and applied chemistry has snowballed. Devoted to the latest achievements of this field, Chemistry of Pyrroles covers the discovery and development of a novel, facile, and highly effective method for the construction of the pyrrole ring from ketones (ketoximes) and acetylene in superbase catalytic systems (Trofimov reaction). It provides cutting-edge details on the preparation of valuable but previously inaccessible pyrrole compounds. It includes approximately 1,000 structures of novel pyrrole compounds, their yields, and physical-chemical characteristics. The authors analyze conditions of typical syntheses, limitations of their applicability, and possibility of vinyl chloride or dichloroethane application instead of acetylene. They examine chemical engineering aspects of the first synthesis of tetrahydroindole and indole from commercially available oxime of cyclohexanone and acetylene. In addition, the book discusses new facets of pyrroles and N-vinyl pyrroles reactivity in the reactions with the participation of both the pyrrole ring and N-vinyl groups. The book provides condensed, clear-cut information on novel syntheses of substituted pyrroles as key structural units of living matter (chlorophyll and hemoglobin), pharmaceuticals, and monomers for optoelectronic materials. It includes tables that provide references to original works, forming a guide to a variety of the reactions and synthesized compounds discussed. With coverage of the broad range of pyrrole chemistry and methods for their synthesis, it provides both a theoretical and an experimental basis for drug design.
(source: Nielsen Book Data)
  • Introduction Synthesis of Pyrroles and N-Vinylpyrroles by the Reaction of Ketones (Ketoximes) with Acetylenes Heterocyclization of ketoximes with acetylene Regioselectivity of the reaction Substituted acetylenes in reactions with ketoximes Vinyl halogenides and dihalogenethanes as synthetic equivalents of acetylene Intermediate stages and side reactions delta-Carbolines from 3-acylindoles and acetylene Reaction of ketoximes with acetylene in the presence of ketones. One-pot assembly of 4-methylen-3-oxa-1-azabicyclo[3.1.0]hexanes Transformations of aldoximes in the systems MOH/DMSO and MOH/DMSO/acetylene Mechanism of pyrrole synthesis from ketoximes and acetylene Novel Aspects of NH- and N-Vinylpyrroles Reactivity Reaction with the participation of the pyrrole ring Reactions with participation of the vinyl group Conclusions References Index.
  • (source: Nielsen Book Data)
During the last 30 years, knowledge of the essential role that pyrrole structures play in the chemistry of living organisms, drug design, and the development of advanced materials has increased. Correspondingly, research on the diverse issues of synthetic, theoretical, and applied chemistry has snowballed. Devoted to the latest achievements of this field, Chemistry of Pyrroles covers the discovery and development of a novel, facile, and highly effective method for the construction of the pyrrole ring from ketones (ketoximes) and acetylene in superbase catalytic systems (Trofimov reaction). It provides cutting-edge details on the preparation of valuable but previously inaccessible pyrrole compounds. It includes approximately 1,000 structures of novel pyrrole compounds, their yields, and physical-chemical characteristics. The authors analyze conditions of typical syntheses, limitations of their applicability, and possibility of vinyl chloride or dichloroethane application instead of acetylene. They examine chemical engineering aspects of the first synthesis of tetrahydroindole and indole from commercially available oxime of cyclohexanone and acetylene. In addition, the book discusses new facets of pyrroles and N-vinyl pyrroles reactivity in the reactions with the participation of both the pyrrole ring and N-vinyl groups. The book provides condensed, clear-cut information on novel syntheses of substituted pyrroles as key structural units of living matter (chlorophyll and hemoglobin), pharmaceuticals, and monomers for optoelectronic materials. It includes tables that provide references to original works, forming a guide to a variety of the reactions and synthesized compounds discussed. With coverage of the broad range of pyrrole chemistry and methods for their synthesis, it provides both a theoretical and an experimental basis for drug design.
(source: Nielsen Book Data)
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD401 .C4955 2015 Unknown
Book
xii, 149 pages : illustrations ; 25 cm
  • Introduction Transition Metal-Catalyzed Asymmetric Epoxidations Manganese Systems Iron and Ruthenium Systems Titanium Systems Systems Based on Other Metals Transition Metal-Catalyzed Asymmetric Sulfoxidations Vanadium Systems Titanium Systems Iron Systems Systems Based on Other Metals Miscellaneous Transition Metal-Catalyzed Asymmetric Oxidations Cis-Dihydroxylations of Olefins Baeyer-Villiger Oxidations Oxidative Kinetic Resolution of Secondary Alcohols and Desymmetrization of Meso-Diols Enantioselective Aerobic Oxidative Coupling of 2-Naphthols Enantioselective C-H Oxidations Organocatalytic Asymmetric Oxidations Epoxidations Miscellaneous Oxidations Fe- and Mn-Based Synthetic Models of Non-Heme Oygenases: Stereospecific C-H Oxidations Iron Systems Manganese Systems Active Species and Mechanisms of Non-Heme Fe- and Mn-Catalyzed Oxidations Iron Systems Manganese Systems Industrial Perspective General Remarks Some Examples Outlook.
  • (source: Nielsen Book Data)
Catalysis plays a vital role in chemical, petroleum, agriculture, polymer, electronics, pharmaceutical, and other industries. Over 90 percent of chemicals originate from catalytic processes. Toughening economic and environmental constraints have proven to be a challenge for meeting the demand of novel efficient and sustainable regio- and stereoselective catalyst systems. Environmentally Sustainable Catalytic Asymmetric Oxidations provides a comprehensive overview of existing ecologically friendly catalyst systems for various asymmetric oxidation processes. Topics include: * A survey of existing transition metal-based catalyst systems for asymmetric epoxidations (AEs) with O2 and H2O2 * Asymmetric sulfoxidations with H2O2 on chiral metal complexes * An overview of various transition metal-catalyzed oxidative transformations with H2O2 or O2 used as the terminal oxidant * Organocatalytic asymmetric oxidations * Catalytic processes of stereospecific oxidations of C-H functional groups * The role that oxoiron(V) intermediates play in chemo- and stereoselective oxidations catalyzed by non-heme iron complexes The book concludes with a discussion of the opportunities and problems associated with the industrial application of stereoselective processes of catalytic oxidation with H2O2 and O2. It also provides examples of processes with industrial potential. Some of the catalysts presented in this book may serve as promising alternatives for existing catalysts-progressively replacing them in manufacturing processes and ultimately making the chemical industry greener and cleaner.
(source: Nielsen Book Data)
  • Introduction Transition Metal-Catalyzed Asymmetric Epoxidations Manganese Systems Iron and Ruthenium Systems Titanium Systems Systems Based on Other Metals Transition Metal-Catalyzed Asymmetric Sulfoxidations Vanadium Systems Titanium Systems Iron Systems Systems Based on Other Metals Miscellaneous Transition Metal-Catalyzed Asymmetric Oxidations Cis-Dihydroxylations of Olefins Baeyer-Villiger Oxidations Oxidative Kinetic Resolution of Secondary Alcohols and Desymmetrization of Meso-Diols Enantioselective Aerobic Oxidative Coupling of 2-Naphthols Enantioselective C-H Oxidations Organocatalytic Asymmetric Oxidations Epoxidations Miscellaneous Oxidations Fe- and Mn-Based Synthetic Models of Non-Heme Oygenases: Stereospecific C-H Oxidations Iron Systems Manganese Systems Active Species and Mechanisms of Non-Heme Fe- and Mn-Catalyzed Oxidations Iron Systems Manganese Systems Industrial Perspective General Remarks Some Examples Outlook.
  • (source: Nielsen Book Data)
Catalysis plays a vital role in chemical, petroleum, agriculture, polymer, electronics, pharmaceutical, and other industries. Over 90 percent of chemicals originate from catalytic processes. Toughening economic and environmental constraints have proven to be a challenge for meeting the demand of novel efficient and sustainable regio- and stereoselective catalyst systems. Environmentally Sustainable Catalytic Asymmetric Oxidations provides a comprehensive overview of existing ecologically friendly catalyst systems for various asymmetric oxidation processes. Topics include: * A survey of existing transition metal-based catalyst systems for asymmetric epoxidations (AEs) with O2 and H2O2 * Asymmetric sulfoxidations with H2O2 on chiral metal complexes * An overview of various transition metal-catalyzed oxidative transformations with H2O2 or O2 used as the terminal oxidant * Organocatalytic asymmetric oxidations * Catalytic processes of stereospecific oxidations of C-H functional groups * The role that oxoiron(V) intermediates play in chemo- and stereoselective oxidations catalyzed by non-heme iron complexes The book concludes with a discussion of the opportunities and problems associated with the industrial application of stereoselective processes of catalytic oxidation with H2O2 and O2. It also provides examples of processes with industrial potential. Some of the catalysts presented in this book may serve as promising alternatives for existing catalysts-progressively replacing them in manufacturing processes and ultimately making the chemical industry greener and cleaner.
(source: Nielsen Book Data)
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD281 .O9 B79 2015 Unknown
Book
xvii, 155 pages ; illustrations ; 23 cm
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD262 .D36 2015 Unavailable In process Request
Book
xvi, 507 pages : illustrations ; 29 cm
Addressing a dynamic aspect of organic chemistry, this book describes synthetic strategies and applications for multicomponent reactions including key routes for synthesizing complex molecules. Illustrates the crucial role and the important utility of multicomponent reactions (MCRs) to organic syntheses Compiles novel and efficient synthetic multicomponent procedures to give readers a complete picture of this class of organic reactions Helps readers to design efficient and practical transformations using multicomponent reaction strategies Describes reaction background, applications to synthesize complex molecules and drugs, and reaction mechanisms.
(source: Nielsen Book Data)
Addressing a dynamic aspect of organic chemistry, this book describes synthetic strategies and applications for multicomponent reactions including key routes for synthesizing complex molecules. Illustrates the crucial role and the important utility of multicomponent reactions (MCRs) to organic syntheses Compiles novel and efficient synthetic multicomponent procedures to give readers a complete picture of this class of organic reactions Helps readers to design efficient and practical transformations using multicomponent reaction strategies Describes reaction background, applications to synthesize complex molecules and drugs, and reaction mechanisms.
(source: Nielsen Book Data)
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD501 .M868 2015 Unknown
Book
xvi, 528 pages : Illustrations ; 26 cm
  • PART I: INTRODUCTION TO THE ORGANIC LABORATORY Essay: Introduction to the Organic Laboratory 1. Safety in the Laboratory 2. Protecting the Environment 3. Laboratory Notebooks and Prelaboratory Information PART II: CARRYING OUT CHEMICAL REACTIONS Essay: Carrying Out Chemical Reactions 4. Laboratory Glassware 5. Measurements and Transferring Reagents 6. Heating and Cooling Methods 7. Carrying out Organic Reactions 8. Computational Chemistry PART III: BASIC METHODS FOR SEPARATION, PURIFICATION, AND ANALYSIS Essay: Intermolecular Forces in Organic Chemistry 9. Filtration 10. Extraction 11. Drying Organic Liquids and Recovering Reaction Products 12. Boiling Points and Distillation 13. Refractometry 14. Melting Points and Melting Ranges 15. Recrystallization 16. Sublimation 17. Optical Activity and Enantiomeric Analysis PART IV: CHROMATOGRAPHY Essay: Modern Chromatographic Separations 18. Thin-Layer Chromatography 19. Liquid Chromatography 20. Gas Chromatography PART V: SPECTROMETRIC CHARACTERIZATION METHODS Essay: The Spectrometric Revolution 21. Infrared Spectroscopy 22. Nuclear Magnetic Resonance Spectroscopy 23. 13C and Two-Dimensional NMR Spectroscopy 24. Mass Spectrometry 25. Ultraviolet and Visible Spectroscopy 26 . Integrated Spectrometry Problems PART VI: DESIGNING AND CARRYING OUT ORGANIC EXPERIMENTS 27. Using the Literature of Organic Chemistry 28. Designing a Chemical Reaction.
  • (source: Nielsen Book Data)
"Laboratory Techniques in Organic Chemistry" is the most comprehensive and detailed presentation of the lab techniques organic chemistry students need to know. Compatible with any organic chemistry lab manual or set of experiments, it combines specific instructions for three different kinds of laboratory glassware: miniscale, standard taper microscale, and Williamson microscale. It is written to provide effective support for guided-inquiry and design-based experiments and projects, as well as for traditional lab experiments.
(source: Nielsen Book Data)
  • PART I: INTRODUCTION TO THE ORGANIC LABORATORY Essay: Introduction to the Organic Laboratory 1. Safety in the Laboratory 2. Protecting the Environment 3. Laboratory Notebooks and Prelaboratory Information PART II: CARRYING OUT CHEMICAL REACTIONS Essay: Carrying Out Chemical Reactions 4. Laboratory Glassware 5. Measurements and Transferring Reagents 6. Heating and Cooling Methods 7. Carrying out Organic Reactions 8. Computational Chemistry PART III: BASIC METHODS FOR SEPARATION, PURIFICATION, AND ANALYSIS Essay: Intermolecular Forces in Organic Chemistry 9. Filtration 10. Extraction 11. Drying Organic Liquids and Recovering Reaction Products 12. Boiling Points and Distillation 13. Refractometry 14. Melting Points and Melting Ranges 15. Recrystallization 16. Sublimation 17. Optical Activity and Enantiomeric Analysis PART IV: CHROMATOGRAPHY Essay: Modern Chromatographic Separations 18. Thin-Layer Chromatography 19. Liquid Chromatography 20. Gas Chromatography PART V: SPECTROMETRIC CHARACTERIZATION METHODS Essay: The Spectrometric Revolution 21. Infrared Spectroscopy 22. Nuclear Magnetic Resonance Spectroscopy 23. 13C and Two-Dimensional NMR Spectroscopy 24. Mass Spectrometry 25. Ultraviolet and Visible Spectroscopy 26 . Integrated Spectrometry Problems PART VI: DESIGNING AND CARRYING OUT ORGANIC EXPERIMENTS 27. Using the Literature of Organic Chemistry 28. Designing a Chemical Reaction.
  • (source: Nielsen Book Data)
"Laboratory Techniques in Organic Chemistry" is the most comprehensive and detailed presentation of the lab techniques organic chemistry students need to know. Compatible with any organic chemistry lab manual or set of experiments, it combines specific instructions for three different kinds of laboratory glassware: miniscale, standard taper microscale, and Williamson microscale. It is written to provide effective support for guided-inquiry and design-based experiments and projects, as well as for traditional lab experiments.
(source: Nielsen Book Data)
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
On reserve: Ask at circulation desk
QD261 .L32 2014 Unknown On Reserve 2-hour loan
QD261 .L32 2014 Unknown On Reserve 2-hour loan
CHEM-130-01, CHEM-130-01
Course
CHEM-130-01 -- Organic and Bio-organic Chemistry Laboratory
Instructor(s)
McClory, Megan Kathleen
Course
CHEM-130-01 -- Organic and Bio-organic Chemistry Laboratory
Instructor(s)
Vollmer-Snarr, Heidi R
Book
xiv, 354 pages : illustrations ; 23 cm
  • Safety first, last, and always
  • Keeping a notebook
  • Interpreting a handbook
  • Jointware.
This book presents the basic techniques of the organic chemistry laboratory with an emphasis on doing the work correctly the first time. New to this edition are discussions on safety in the laboratory with new consideration of the addition of such technology as the iPad, Nook, Kindle, and even text messaging. Updated discussion is added on Microscale; a number of NMR spectra have been added, with basic interpretation and suggestions on presentation of the data; and lastly, presentation of a more modern outline of the instrumentation of HPLC is included.
(source: Nielsen Book Data)
  • Safety first, last, and always
  • Keeping a notebook
  • Interpreting a handbook
  • Jointware.
This book presents the basic techniques of the organic chemistry laboratory with an emphasis on doing the work correctly the first time. New to this edition are discussions on safety in the laboratory with new consideration of the addition of such technology as the iPad, Nook, Kindle, and even text messaging. Updated discussion is added on Microscale; a number of NMR spectra have been added, with basic interpretation and suggestions on presentation of the data; and lastly, presentation of a more modern outline of the instrumentation of HPLC is included.
(source: Nielsen Book Data)
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Permanent reserve: Ask at circulation desk
QD261 .Z83 2014 Unknown
QD261 .Z83 2014 Unknown
QD261 .Z83 2014 Unknown
QD261 .Z83 2014 Unknown
QD261 .Z83 2014 Unknown
QD261 .Z83 2014 Unknown

17. Organic chemistry [2014]

Book
1 v. (various pagings) : ill. (some col.) ; 29 cm
  • Preface Prologue Chapter 1 Structure and Bonding Chapter 2 Acids and Bases Chapter 3 Introduction to Organic Molecules and Functional Groups Chapter 4 Alkanes Chapter 5 Stereochemistry Chapter 6 Understanding Organic Reactions Chapter 7 Alkyl Halides and Nucleophilic Substitution Chapter 8 Alkyl Halides and Elimination Reactions Chapter 9 Alcohols, Ethers, and Epoxides Chapter 10 Alkenes Chapter 11 Alkynes Chapter 12 Oxidation and Reduction Chapter 13 Mass Spectrometry and Infrared Spectroscopy Chapter 14 Nuclear Magnetic Resonance Spectroscopy Chapter 15 Radical Reactions Chapter 16 Conjugation, Resonance, and Dienes Chapter 17 Benzene and Aromatic Compounds Chapter 18 Reactions of Aromatic Compounds Chapter 19 Carboxylic Acids and Acidity of the O-H Bond Chapter 20 Introduction to Carbonyl Chemistry: Organometallic Reagents-- Oxidation and Reduction Chapter 21 Aldehydes and Ketones-Nucleophilic Addition Chapter 22 Carboxylic Acids and Their Derivatives-Nucleophilic Acyl Substitution Chapter 23 Substitution Reactions of Carbonyl Compounds at the a-Carbon Chapter 24 Carbonyl Condensation Reactions Chapter 25 Amines Chapter 26 Carbon-Carbon Bond-Forming Reactions in Organic Synthesis Chapter 27 Pericyclic Reactions Chapter 28 Carbohydrates Chapter 29 Amino Acids and Proteins Chapter 30 Lipids Chapter 31 Synthetic Polymers Appendices Glossary Credits Index.
  • (source: Nielsen Book Data)
Serious Science with an Approach Built for Today's Students. Smith's "Organic Chemistry" continues to breathe new life into the organic chemistry world. This new fourth edition retains its popular delivery of organic chemistry content in a student-friendly format. Janice Smith draws on her extensive teaching background to deliver organic chemistry in a way in which students learn: with limited use of text paragraphs, and through concisely written bulleted lists and highly detailed, well-labeled "teaching" illustrations. Don't make your text decision without seeing "Organic Chemistry, 4th edition" by Janice Gorzynski Smith!.
(source: Nielsen Book Data)
  • Preface Prologue Chapter 1 Structure and Bonding Chapter 2 Acids and Bases Chapter 3 Introduction to Organic Molecules and Functional Groups Chapter 4 Alkanes Chapter 5 Stereochemistry Chapter 6 Understanding Organic Reactions Chapter 7 Alkyl Halides and Nucleophilic Substitution Chapter 8 Alkyl Halides and Elimination Reactions Chapter 9 Alcohols, Ethers, and Epoxides Chapter 10 Alkenes Chapter 11 Alkynes Chapter 12 Oxidation and Reduction Chapter 13 Mass Spectrometry and Infrared Spectroscopy Chapter 14 Nuclear Magnetic Resonance Spectroscopy Chapter 15 Radical Reactions Chapter 16 Conjugation, Resonance, and Dienes Chapter 17 Benzene and Aromatic Compounds Chapter 18 Reactions of Aromatic Compounds Chapter 19 Carboxylic Acids and Acidity of the O-H Bond Chapter 20 Introduction to Carbonyl Chemistry: Organometallic Reagents-- Oxidation and Reduction Chapter 21 Aldehydes and Ketones-Nucleophilic Addition Chapter 22 Carboxylic Acids and Their Derivatives-Nucleophilic Acyl Substitution Chapter 23 Substitution Reactions of Carbonyl Compounds at the a-Carbon Chapter 24 Carbonyl Condensation Reactions Chapter 25 Amines Chapter 26 Carbon-Carbon Bond-Forming Reactions in Organic Synthesis Chapter 27 Pericyclic Reactions Chapter 28 Carbohydrates Chapter 29 Amino Acids and Proteins Chapter 30 Lipids Chapter 31 Synthetic Polymers Appendices Glossary Credits Index.
  • (source: Nielsen Book Data)
Serious Science with an Approach Built for Today's Students. Smith's "Organic Chemistry" continues to breathe new life into the organic chemistry world. This new fourth edition retains its popular delivery of organic chemistry content in a student-friendly format. Janice Smith draws on her extensive teaching background to deliver organic chemistry in a way in which students learn: with limited use of text paragraphs, and through concisely written bulleted lists and highly detailed, well-labeled "teaching" illustrations. Don't make your text decision without seeing "Organic Chemistry, 4th edition" by Janice Gorzynski Smith!.
(source: Nielsen Book Data)
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Permanent reserve: Ask at circulation desk
QD253.2 .S63 2014 Unknown

18. Organic chemistry [2014]

Book
1 v. (various pagings) : col. ill. ; 28 cm.
All of Paula Bruice's extensive revisions to the Seventh Edition of Organic Chemistry follow a central guiding principle: support what modern students need in order to understand and retain what they learn in organic chemistry for successful futures in industry, research, and medicine. In consideration of today's classroom dynamics and the changes coming to the 2015 MCAT, this revision offers a completely new design with enhanced art throughout, reorganization of materials to reinforce fundamental skills and facilitate more efficient studying.
(source: Nielsen Book Data)
All of Paula Bruice's extensive revisions to the Seventh Edition of Organic Chemistry follow a central guiding principle: support what modern students need in order to understand and retain what they learn in organic chemistry for successful futures in industry, research, and medicine. In consideration of today's classroom dynamics and the changes coming to the 2015 MCAT, this revision offers a completely new design with enhanced art throughout, reorganization of materials to reinforce fundamental skills and facilitate more efficient studying.
(source: Nielsen Book Data)
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD251.3 .B78 2014 Unknown

19. Organic chemistry [2014]

Book
xxxvi, 1139, [25] pages : illustrations (some color) ; 29 cm
  • Machine generated contents note: 1.The Basics: Bonding and Molecular Structure 2. Families of Carbon Compounds : Functional Groups, Intermolecular Forces, and Infrared (IR) 3. An Introduction to Organic Reactions and Their Mechanisms: Acids and Bases 4. Nomenclature and Conformations of Alkanes and Cycloalkanes 5. Stereochemistry: Chiral Molecules 6. Ionic Reactions : Nucleophilic Substitution & Elimination Reactions of Alkyl Halides 7. Alkenes & Alkynes I: Properties & Synthesis. Elimination Reactions of Alkyl Halides 8. Alkenes & Alkynes II: Addition Reactions 9. Nuclear Magnetic Resonance and Mass Spectroscopy: Tools for Structure Determination 10. Radical Reactions 11. Alcohols & Ethers 12. Alcohols from Carbonyl Compounds : Oxidation-Reduction & Organometallic Compounds 13. Conjugated Unsaturated Systems 14. Aromatic Compounds 15. Reactions of Aromatic Compounds 16. Aldehydes & Ketones: Nucleophilic Addition to the Carbonyl Group 17. Carboxylic Acids and Their Derivatives: Nucleophilic Addition-Elimination at the Acyl Carbon 18. Reactions at the [alpha] Carbon of Carbonyl Compounds: Enols and Enolates 19. Condensation and Conjugate Addition Reactions of Carbonyl Compounds : More Chemistry of Enolates 20. Amines 21. Phenols & Aryl Halides: Nucleophilic Aromatic SubstitutionSpecial Topic G: Carbon-Carbon Bond-Forming and Other Reactions of Transition Metal Organometallic Compounds 22. Carbohydrates 23. Lipids 24. Amino Acids & Proteins 25. Nucleic Acids & Protein Synthesis .
"Now in a new edition, this book continues its tradition of excellence in teaching and preparing students for success in the organic classroom and beyond. A central theme of the authors' approach to organic chemistry is to emphasize the relationship between structure and reactivity. To accomplish this, the text is organized in a way that combines the most useful features of a functional group approach with one largely based on reaction mechanisms. Emphasizing mechanisms and their common aspects as often as possible, this book shows students what organic chemistry is, how it works, and what it does in living systems and the physical world around us"-- Provided by publisher.
  • Machine generated contents note: 1.The Basics: Bonding and Molecular Structure 2. Families of Carbon Compounds : Functional Groups, Intermolecular Forces, and Infrared (IR) 3. An Introduction to Organic Reactions and Their Mechanisms: Acids and Bases 4. Nomenclature and Conformations of Alkanes and Cycloalkanes 5. Stereochemistry: Chiral Molecules 6. Ionic Reactions : Nucleophilic Substitution & Elimination Reactions of Alkyl Halides 7. Alkenes & Alkynes I: Properties & Synthesis. Elimination Reactions of Alkyl Halides 8. Alkenes & Alkynes II: Addition Reactions 9. Nuclear Magnetic Resonance and Mass Spectroscopy: Tools for Structure Determination 10. Radical Reactions 11. Alcohols & Ethers 12. Alcohols from Carbonyl Compounds : Oxidation-Reduction & Organometallic Compounds 13. Conjugated Unsaturated Systems 14. Aromatic Compounds 15. Reactions of Aromatic Compounds 16. Aldehydes & Ketones: Nucleophilic Addition to the Carbonyl Group 17. Carboxylic Acids and Their Derivatives: Nucleophilic Addition-Elimination at the Acyl Carbon 18. Reactions at the [alpha] Carbon of Carbonyl Compounds: Enols and Enolates 19. Condensation and Conjugate Addition Reactions of Carbonyl Compounds : More Chemistry of Enolates 20. Amines 21. Phenols & Aryl Halides: Nucleophilic Aromatic SubstitutionSpecial Topic G: Carbon-Carbon Bond-Forming and Other Reactions of Transition Metal Organometallic Compounds 22. Carbohydrates 23. Lipids 24. Amino Acids & Proteins 25. Nucleic Acids & Protein Synthesis .
"Now in a new edition, this book continues its tradition of excellence in teaching and preparing students for success in the organic classroom and beyond. A central theme of the authors' approach to organic chemistry is to emphasize the relationship between structure and reactivity. To accomplish this, the text is organized in a way that combines the most useful features of a functional group approach with one largely based on reaction mechanisms. Emphasizing mechanisms and their common aspects as often as possible, this book shows students what organic chemistry is, how it works, and what it does in living systems and the physical world around us"-- Provided by publisher.
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD253.2 .S65 2014 Unknown

20. Organic chemistry [2014]

Book
1 volume (various pagings) : illustrations (chiefly color) ; 28 cm
  • 1 Structure Determines Properties 2 Alkanes and Cycloakanes: Introduction to Hydrocarbons 3 Alkanes and Cycloalkanes: Introduction to StereoChemistry 4 Alcohols and Alkyl Halides: Introduction to Reaction Mechanisms 5 Structure and Preparation of Alkenes: Elimination Reactions 6 Addition Reactions of Alkenes 7 Chirality 8 Nucleophilic Substitution 9 Alkynes 10 Conjugation in Alkadienes and Allylic Systems 11 Arenes and Aromaticity 12 Electrophilic and Nucleophilic Aromatic Substitution 13 Spectroscopy 14 Organometallic Compounds 15 Alcohols, Diols, and Thiols 16 Ethers, Epoxides, and Sulfides 17 Aldehydes and Ketones: Nucleophilic Addition to the Carbonyl Group 18 Carboxylic Acids 19 Acid Derivatives 20 Enols and Enolates 21 Amines 22 Phenols 23 Carbohydrates 24 Lipids 25 Amino Acids, Peptides, and Proteins 26 Nucleosides, Nucleotides, and Nucleic Acids 27 Synthetic Polymers Appendix 1 Physical Properties Appendix 2 Answers to In-Text Problems GLOSSARY CREDITS INDEX.
  • (source: Nielsen Book Data)
"A Market Leading, Traditional Approach to Organic Chemistry" For nine editions, "Organic Chemistry" has been designed to meet the needs of the "mainstream, " two-semester, undergraduate organic chemistry course. This best-selling text gives students a solid understanding of organic chemistry by stressing how fundamental reaction mechanisms function and reactions occur.
(source: Nielsen Book Data)
  • 1 Structure Determines Properties 2 Alkanes and Cycloakanes: Introduction to Hydrocarbons 3 Alkanes and Cycloalkanes: Introduction to StereoChemistry 4 Alcohols and Alkyl Halides: Introduction to Reaction Mechanisms 5 Structure and Preparation of Alkenes: Elimination Reactions 6 Addition Reactions of Alkenes 7 Chirality 8 Nucleophilic Substitution 9 Alkynes 10 Conjugation in Alkadienes and Allylic Systems 11 Arenes and Aromaticity 12 Electrophilic and Nucleophilic Aromatic Substitution 13 Spectroscopy 14 Organometallic Compounds 15 Alcohols, Diols, and Thiols 16 Ethers, Epoxides, and Sulfides 17 Aldehydes and Ketones: Nucleophilic Addition to the Carbonyl Group 18 Carboxylic Acids 19 Acid Derivatives 20 Enols and Enolates 21 Amines 22 Phenols 23 Carbohydrates 24 Lipids 25 Amino Acids, Peptides, and Proteins 26 Nucleosides, Nucleotides, and Nucleic Acids 27 Synthetic Polymers Appendix 1 Physical Properties Appendix 2 Answers to In-Text Problems GLOSSARY CREDITS INDEX.
  • (source: Nielsen Book Data)
"A Market Leading, Traditional Approach to Organic Chemistry" For nine editions, "Organic Chemistry" has been designed to meet the needs of the "mainstream, " two-semester, undergraduate organic chemistry course. This best-selling text gives students a solid understanding of organic chemistry by stressing how fundamental reaction mechanisms function and reactions occur.
(source: Nielsen Book Data)
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD251.3 .C37 2014 Unknown

Looking for different results?

Modify your search: Remove limit(s) Search all fields

Search elsewhere: Search WorldCat Search library website