Search results

286 results

View results as:
Number of results to display per page
Book
xvi, 381 pages : illustrations ; 25 cm
  • Chapter 1. Synthesis of pyrroles and N-vinylpyrroles by the reaction of ketones (ketoximes) with acetylenes
  • chapter 2. Novel aspects of NH- and N-vinylpyrroles reactivity.
  • Chapter 1. Synthesis of pyrroles and N-vinylpyrroles by the reaction of ketones (ketoximes) with acetylenes
  • chapter 2. Novel aspects of NH- and N-vinylpyrroles reactivity.
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
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD281 .O9 B79 2015 Unknown
Book
xvi, 528 pages : Illustrations ; 26 cm
  • Part 1: Introduction to the organic laboratory. Essay: The role of the laboratory
  • Part 2: Carrying out chemical reactions. Essay: Learning to do organic chemistry
  • Part 3: Basic methods for separation, purification, and analysis. Essay: Intermolecular forces in organic chemistry
  • Part 4: Chromotography. Essay: Modern chromatographic separations
  • Part 5: Spectroscopic methods. Essay: The spectroscopic revolution
  • Part 6: Designing and carrying out organic experiments. Essay: Inquiry-driven lab experiments.
  • Part 1: Introduction to the organic laboratory. Essay: The role of the laboratory
  • Part 2: Carrying out chemical reactions. Essay: Learning to do organic chemistry
  • Part 3: Basic methods for separation, purification, and analysis. Essay: Intermolecular forces in organic chemistry
  • Part 4: Chromotography. Essay: Modern chromatographic separations
  • Part 5: Spectroscopic methods. Essay: The spectroscopic revolution
  • Part 6: Designing and carrying out organic experiments. Essay: Inquiry-driven lab experiments.
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Request at circulation desk
QD261 .L32 2014 Unknown On Reserve 2-hour loan
QD261 .L32 2014 Unknown On Reserve 2-hour loan
CHEM-130-01
Course
CHEM-130-01 -- Organic Chemistry Laboratory II
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
Request at circulation desk
QD261 .Z83 2014 Unknown On Reserve 2-hour loan
QD261 .Z83 2014 Unknown On Reserve 2-hour loan
QD261 .Z83 2014 Unknown On Reserve 2-hour loan
QD261 .Z83 2014 Unknown On Reserve 2-hour loan
QD261 .Z83 2014 Unknown On Reserve 2-hour loan
QD261 .Z83 2014 Unknown On Reserve 2-hour loan
CHEM-130-01
Course
CHEM-130-01 -- Organic Chemistry Laboratory II
Instructor(s)
Vollmer-Snarr, Heidi R

5. 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

6. Organic chemistry [2014]

Book
1 volume (various pagings) : illustrations (chiefly color) ; 28 cm
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD251.3 .C37 2014 Unknown

7. Organic chemistry [2014]

Book
1 v. (various pagings) : ill. (some col.) ; 29 cm
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Permanent reserve
QD253.2 .S63 2014 Unknown

8. 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

9. Organic chemistry [2015]

Book
xxxvii, 1247 pages : illustrations (chiefly color) ; 29 cm
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Request at circulation desk
QD253 .J65 2014 Unknown On Reserve 2-hour loan
QD253 .J65 2014 Unknown On Reserve 2-hour loan
QD253 .J65 2014 Unknown On Reserve 2-hour loan
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
Book
xxxii, 648 pages : illustrations (colour) ; 27 cm
This title combines a focus on core topics and themes with a mechanistical approach to the explanation of the reactions it describes, making it ideal for those looking for a solid understanding of the central themes of organic chemistry.
This title combines a focus on core topics and themes with a mechanistical approach to the explanation of the reactions it describes, making it ideal for those looking for a solid understanding of the central themes of organic chemistry.
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD251.3 .O38 2014 Unknown
Book
(various pagings) : illustrations (some color) ; 29 cm
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD253.2 .K375 2014 Unknown
Book
x, 283 pages : illustrations (some color) ; 25 cm
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD476 .S54 2014 Unknown
Book
1 volume (various pagings) : illustrations ; 28 cm
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Permanent reserve
QD253.2 .S65 2014 Unknown
Book
vi, 950 pages : ill. ; 28 cm
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Request at circulation desk
QD253 .J65 2014 GUIDE Unknown On Reserve 2-hour loan
QD253 .J65 2014 GUIDE Unknown On Reserve 2-hour loan
QD253 .J65 2014 GUIDE Unknown On Reserve 2-hour loan
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
Book
xxv, 330 p. : ill. ; 23 cm.
  • General introduction Safety Safety is your primary responsibility Safe working practice Safety risk assessments Common hazards Accident and emergency procedures Bibliography Keeping records of laboratory work Introduction The laboratory notebook Keeping records of data Some tips on report and thesis preparation References Equipping the laboratory and the bench Introduction Setting up the laboratory General laboratory equipment The individual bench Equipment for parallel experiments Equipment for controlled experimentation Purification and drying of solvents Introduction Purification of solvents Drying agents Drying of solvents References Reagents: Preparation, purification, and handling Introduction Classification of reagents for handling Techniques for obtaining pure and dry reagents Techniques for handling and measuring reagents Preparation and titration of simple organometallic reagents and lithium amide bases Preparation of diazomethane References Gases Introduction Use of gas cylinders Handling gases Measurement of gases Inert gases Reagent gases References Vacuum pumps Introduction House vacuum systems (low vacuum) Medium vacuum pumps High vacuum pumps Pressure measurement and regulation Carrying out the reaction Introduction Reactions with air-sensitive reagents Reaction monitoring Reactions at other than room temperature Driving equilibria Agitation Use of controlled reactor systems References Working up the reaction Introduction Quenching the reaction Isolation of the crude product Data that need to be collected on the crude product prior to purification Purification Introduction Crystallization Distillation Sublimation Flash chromatography Dry-column flash chromatography Preparative TLC Medium pressure and prepacked chromatography systems Preparative HPLC References Small-scale reactions Introduction Reactions at or below room temperature Reactions above room temperature Reactions in NMR tubes Purification of materials Large-scale reactions Introduction Carrying out the reaction Workup and product isolation Purification of the products Special procedures Introduction Catalytic hydrogenation Photolysis Ozonolysis Flash vacuum pyrolysis (FVP) Liquid ammonia reactions Microwave reactions References Characterization Introduction NMR spectra IR spectra UV spectroscopy Mass spectrometry Melting point (m.p.) and boiling point (b.p.) Optical rotation Microanalysis Keeping the data Troubleshooting: What to do when things don't work The chemical literature The structure of the chemical literature Some important paper-based sources of chemical information Some important electronic-based sources of chemical information How to find chemical information Current awareness References Appendices Properties of common solvents Properties of common gases Approximate pKa values for some common reagents versus common bases Common Bronsted acids Common Lewis acids Common reducing reagents Common oxidizing reagents Index.
  • (source: Nielsen Book Data)
Any research that uses new organic chemicals, or ones that are not commercially available, will at some time require the synthesis of such compounds. Therefore, organic synthesis is important in many areas of both applied and academic research, from chemistry to biology, biochemistry, and materials science. The third edition of a bestseller, Advanced Practical Organic Chemistry is a guide that explains the basic techniques of organic chemistry, presenting the necessary information for readers to carry out widely used modern organic synthesis reactions. This book is written for advanced undergraduate and graduate students as well as industrial organic chemists, particularly those involved in pharmaceutical, agrochemical, and other areas of fine chemical research. It provides the novice or nonspecialist with the often difficult-to-find information on reagent properties needed to perform general techniques. With over 80 years combined experience training and developing organic research chemists in industry and academia, the authors offer sufficient guidance for researchers to perform reactions under conditions that give the highest chance of success, including the appropriate precautions to take and proper experimental protocols. The text also covers the following topics: * Record keeping and equipment * Solvent purification and reagent preparation * Using gases and working with vacuum pumps * Purification, including crystallization and distillation * Small-scale and large-scale reactions * Characterization, including NMR spectra, melting point and boiling point, and microanalysis * Efficient ways to find information in the chemical literature With fully updated text and all newly drawn figures, the third edition provides a powerful tool for building the knowledge on the most up-to-date techniques commonly used in organic synthesis.
(source: Nielsen Book Data)
  • General introduction Safety Safety is your primary responsibility Safe working practice Safety risk assessments Common hazards Accident and emergency procedures Bibliography Keeping records of laboratory work Introduction The laboratory notebook Keeping records of data Some tips on report and thesis preparation References Equipping the laboratory and the bench Introduction Setting up the laboratory General laboratory equipment The individual bench Equipment for parallel experiments Equipment for controlled experimentation Purification and drying of solvents Introduction Purification of solvents Drying agents Drying of solvents References Reagents: Preparation, purification, and handling Introduction Classification of reagents for handling Techniques for obtaining pure and dry reagents Techniques for handling and measuring reagents Preparation and titration of simple organometallic reagents and lithium amide bases Preparation of diazomethane References Gases Introduction Use of gas cylinders Handling gases Measurement of gases Inert gases Reagent gases References Vacuum pumps Introduction House vacuum systems (low vacuum) Medium vacuum pumps High vacuum pumps Pressure measurement and regulation Carrying out the reaction Introduction Reactions with air-sensitive reagents Reaction monitoring Reactions at other than room temperature Driving equilibria Agitation Use of controlled reactor systems References Working up the reaction Introduction Quenching the reaction Isolation of the crude product Data that need to be collected on the crude product prior to purification Purification Introduction Crystallization Distillation Sublimation Flash chromatography Dry-column flash chromatography Preparative TLC Medium pressure and prepacked chromatography systems Preparative HPLC References Small-scale reactions Introduction Reactions at or below room temperature Reactions above room temperature Reactions in NMR tubes Purification of materials Large-scale reactions Introduction Carrying out the reaction Workup and product isolation Purification of the products Special procedures Introduction Catalytic hydrogenation Photolysis Ozonolysis Flash vacuum pyrolysis (FVP) Liquid ammonia reactions Microwave reactions References Characterization Introduction NMR spectra IR spectra UV spectroscopy Mass spectrometry Melting point (m.p.) and boiling point (b.p.) Optical rotation Microanalysis Keeping the data Troubleshooting: What to do when things don't work The chemical literature The structure of the chemical literature Some important paper-based sources of chemical information Some important electronic-based sources of chemical information How to find chemical information Current awareness References Appendices Properties of common solvents Properties of common gases Approximate pKa values for some common reagents versus common bases Common Bronsted acids Common Lewis acids Common reducing reagents Common oxidizing reagents Index.
  • (source: Nielsen Book Data)
Any research that uses new organic chemicals, or ones that are not commercially available, will at some time require the synthesis of such compounds. Therefore, organic synthesis is important in many areas of both applied and academic research, from chemistry to biology, biochemistry, and materials science. The third edition of a bestseller, Advanced Practical Organic Chemistry is a guide that explains the basic techniques of organic chemistry, presenting the necessary information for readers to carry out widely used modern organic synthesis reactions. This book is written for advanced undergraduate and graduate students as well as industrial organic chemists, particularly those involved in pharmaceutical, agrochemical, and other areas of fine chemical research. It provides the novice or nonspecialist with the often difficult-to-find information on reagent properties needed to perform general techniques. With over 80 years combined experience training and developing organic research chemists in industry and academia, the authors offer sufficient guidance for researchers to perform reactions under conditions that give the highest chance of success, including the appropriate precautions to take and proper experimental protocols. The text also covers the following topics: * Record keeping and equipment * Solvent purification and reagent preparation * Using gases and working with vacuum pumps * Purification, including crystallization and distillation * Small-scale and large-scale reactions * Characterization, including NMR spectra, melting point and boiling point, and microanalysis * Efficient ways to find information in the chemical literature With fully updated text and all newly drawn figures, the third edition provides a powerful tool for building the knowledge on the most up-to-date techniques commonly used in organic synthesis.
(source: Nielsen Book Data)
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Request at circulation desk
QD262 .A34 2013 Unknown On Reserve 2-hour loan
CHEM-132-01
Course
CHEM-132-01 -- Synthesis Laboratory
Instructor(s)
Cox, Charles
Book
xv, 432 pages : illustrations ; 26 cm
  • 1. Bonding and Electron Distribution
  • 2. The Process of Bond Formation
  • 3. Proton Transfer and the Principles of Stability
  • 4. Important Reaction Archetypes
  • 5. Classification of Electron Sources
  • 6. Classification of Electron Sinks
  • 7. The Electron Flow Pathways
  • 8. Interaction of Electron Sources and Sinks
  • 9. Decisions, Decisions
  • 10. Choosing the Most Probable Path
  • 11. One-Electron Processes
  • 12. Qualitative Molecular Orbital Theory and Pericyclic Reactions
  • Appendix (A Collection of Important Tools).
"The revised 2nd edition builds on and improves this legacy, continuing the rigorous mechanistic approach to organic chemistry. Each mechanistic process is divided into its basic units, the dozen common electron flow pathways that become the building blocks of all the common mechanistic processes"-- Provided by publisher.
  • 1. Bonding and Electron Distribution
  • 2. The Process of Bond Formation
  • 3. Proton Transfer and the Principles of Stability
  • 4. Important Reaction Archetypes
  • 5. Classification of Electron Sources
  • 6. Classification of Electron Sinks
  • 7. The Electron Flow Pathways
  • 8. Interaction of Electron Sources and Sinks
  • 9. Decisions, Decisions
  • 10. Choosing the Most Probable Path
  • 11. One-Electron Processes
  • 12. Qualitative Molecular Orbital Theory and Pericyclic Reactions
  • Appendix (A Collection of Important Tools).
"The revised 2nd edition builds on and improves this legacy, continuing the rigorous mechanistic approach to organic chemistry. Each mechanistic process is divided into its basic units, the dozen common electron flow pathways that become the building blocks of all the common mechanistic processes"-- Provided by publisher.
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD251.3 .S38 2013 Unknown
Book
xxv, 2047 pages : illustrations ; 26 cm
  • PREFACE xiii COMMON ABBREVIATIONS xxi BIOGRAPHICAL STATEMENT xxv PART I INTRODUCTION 1 1. Localized Chemical Bonding 3 1.A. Covalent Bonding 3 1.B. Multiple Valence 6 1.C. Hybridization 7 1.D. Multiple Bonds 9 1.E. Photoelectron Spectroscopy 11 1.F. Electronic Structures of Molecules 14 1.G. Electronegativity 15 1.H. Dipole Moment 18 1.I. Inductive and Field Effects 19 1.J. Bond Distances 21 1.K. Bond Angles 25 1.L. Bond Energies 27 2. Delocalized Chemical Bonding 31 2.A. Molecular Orbitals 32 2.B. Bond Energies and Distances in Compounds Containing Delocalized Bonds 35 2.C. Molecules that have Delocalized Bonds 37 2.D. Cross-Conjugation 42 2.E. The Rules of Resonance 43 2.F. The Resonance Effect 45 2.G. Steric Inhibition of Resonance and the Influences of Strain 46 2.H. pp-dp Bonding. Ylids 49 2.I. Aromaticity 50 2.J. Alternant and Nonalternant Hydrocarbons 63 2.K. Aromatic Systems with Electron Numbers other than Six 65 2.L. Other Aromatic Compounds 82 2.M. Hyperconjugation 85 2.N. Tautomerism 89 3. Bonding Weaker Than Covalent 96 3.A. Hydrogen Bonding 96 3.B. p-p Interactions 103 3.C. Addition Compounds 104 3.D. Catenanes and Rotaxanes 118 3.E. Cucurbit[n]Uril-Based Gyroscane 121 4. Stereochemistry and Conformation 122 4.A. Optical Activity and Chirality 122 4.B. What Kinds of Molecules Display Optical Activity? 125 4.C. The Fischer Projection 136 4.D. Absolute Configuration 137 4.E. The Cause of Optical Activity 145 4.F. Molecules with more than One Stereogenic Center 146 4.G. Asymmetric Synthesis 149 4.H. Methods of Resolution 154 4.I. Optical Purity 160 4.J. cis trans Isomerism 162 4.K. Out-In Isomerism 168 4.L. Enantiotopic and Diastereotopic Atoms, Groups, and Faces 170 4.M. Stereospecific and Stereoselective Syntheses 173 4.N. Conformational Analysis 173 4.O. Molecular Mechanics 190 4.P. STRAIN 192 5. Carbocations, Carbanions, Free Radicals, Carbenes, and Nitrenes 208 5.A. Carbocations 208 5.B. Carbanions 221 5.C. Free Radicals 234 5.D. Carbenes 249 5.E. Nitrenes 257 6. Mechanisms and Methods of Determining them 261 6.A. Types of Mechanism 261 6.B. Types of Reaction 262 6.C. Thermodynamic Requirements for Reaction 264 6.D. Kinetic Requirements for Reaction 266 6.E. The Baldwin Rules for Ring Closure 270 6.F. Kinetic and Thermodynamic Control 271 6.G. The Hammond Postulate 272 6.H. Microscopic Reversibility 273 6.I. Marcus Theory 273 6.J. Methods of Determining Mechanisms 275 7. Irradiation Processes in Organic Chemistry 289 7.A. Photochemistry 289 7.B. Sonochemistry 307 7.C. Microwave Chemistry 309 8. Acids and Bases 312 8.A. Bronsted Theory 312 8.B. The Mechanism of Proton-Transfer Reactions 323 8.C. Measurements of Solvent Acidity 324 8.D. Acid and Base Catalysis 327 8.E. Lewis Acids and Bases 330 8.F. The Effects of Structure on the Strengths of Acids and Bases 334 8.G. The Effects of the Medium on Acid and Base Strength 343 9. Effects of Structure and Medium on Reactivity 347 9.A. Resonance and Field Effects 347 9.B. Steric Effects 349 9.C. Quantitative Treatments of the Effect of Structure on Reactivity 352 9.D. Effect of Medium on Reactivity and Rate 361 PART II INTRODUCTION 367 10. Aliphatic Substitution, Nucleophilic and Organometallic 373 10.A. Mechanisms 373 10.B. SET Mechanisms 389 10.C. The Neighboring-Group Mechanism 391 10.D. The SNi Mechanism 408 10.E. Nucleophilic Substitution at an Allylic Carbon: Allylic Rearrangements 409 10.F. Nucleophilic Substitution at an Aliphatic Trigonal Carbon: The Tetrahedral Mechanism 413 10.G. Reactivity 417 10.H. Reactions 451 11. Aromatic Substitution, Electrophilic 569 11.A. Mechanisms 569 11.B. Orientation and Reactivity 576 11.C. Quantitative Treatments of Reactivity in the Substrate 586 11.D.A Quantitative Treatment of Reactivity of the Electrophile: The Selectivity Relationship 588 11.E. The Effect of the Leaving Group 591 11.F. Reactions 591 12. Aliphatic, Alkenyl, and Alkynyl Substitution, Electrophilic and Organometallic 649 12.A. Mechanisms 650 12.B. Reactivity 658 12.C. Reactions 660 13. Aromatic Substitution: Nucleophilic and Organometallic 732 13.A. Mechanisms 732 13.B. Reactivity 741 13.C. Reactions 745 14. Substitution Reactions: Radical 803 14.A. Mechanisms 803 14.B. Reactivity 812 14.C. Reactions 821 15. Addition to Carbon-Carbon Multiple Bonds 859 15.A. Mechanisms 859 15.B. Orientation and Reactivity 871 15.C. Reactions 881 16. Addition to Carbon-Hetero Multiple Bonds 1067 16.A. Mechanism and Reactivity 1067 16.B. Reactions 1075 17. Eliminations 1253 17.A. Mechanisms and Orientation 1253 17.B. Regiochemistry of the Double Bond 1269 17.C. Stereochemistry of the Double Bond 1273 17.D. Reactivity 1274 17.E. Mechanisms and Orientation in Pyrolytic Eliminations 1278 17.F. Reactions 1282 18. Rearrangements 1321 18.A. Mechanisms 1322 18.B. Longer Nucleophilic Rearrangements 1331 18.C. Free Radical Rearrangements 1333 18.D. Carbene Rearrangements 1337 18.E. Electrophilic Rearrangements 1337 18.F. Reactions 1337 19. Oxidations and Reductions 1433 19.A. Mechanisms 1434 19.B. Reactions 1436 APPENDIX A: THE LITERATURE OF ORGANIC CHEMISTRY 1569 APPENDIX B: CLASSIFICATION OF REACTIONS BY TYPE OF COMPOUNDS SYNTHESIZED 1605 INDEXES AUTHOR INDEX 1631 SUBJECT INDEX 1835.
  • (source: Nielsen Book Data)
The new, revised and updated 7th edition of March's Advanced Organic Chemistry clearly explains the theories and examples of organic chemistry, providing the most comprehensive resource about organic chemistry available. Readers are guided on planning and execution of multi-step synthetic reactions, with detailed descriptions of all the reactions. The first five chapters deal with the structure of organic compounds and discuss important organic chemistry bonds, fundamental principles of conformation, and stereochemistry of organic molecules, and reactive intermediates in organic chemistry. Chapters 6 to 9 are concerned with general principles of mechanism in organic chemistry, including acids and bases, photochemistry, sonochemistry and microwave irradiation, and finally the relationship between structure and reactivity. The last 10 chapters cover the nature and the scope of organic reactions and their mechanisms. The 7th edition proves again it is a must-have desktop reference and textbook for every student and professional working in organic chemistry or related fields. Key features of the 7th edition: * Every chapter has been updated with the most recent reaction information with references to both the primary and review literature * New to the 7th edition: 5,500 references since the last edition, updates / rewrites of the retained sections, and an updated index in Appendix B * Contains more than 1650 reactions and 20,000 valuable references to the primary literature * Includes appendices on the literature of organic chemistry and the classification of reactions according to the compounds synthesized * Guides the reader on planning and execution of multi-step synthetic reactions, with detailed descriptions of all the reactions. Reviews of the previous edition: "...a favorite general organic chemistry text and an easy-to-use one-volume reference. We are confident that this book will remain a dominant reference and that it will reside on many chemists' personal bookshelves." --Journal of Medicinal Chemistry "Who can hope to be seriously accepted as a member of the organic chemistry community without being in possession of at least one edition of 'March'?" --Chemistry and Industry.
(source: Nielsen Book Data)
  • PREFACE xiii COMMON ABBREVIATIONS xxi BIOGRAPHICAL STATEMENT xxv PART I INTRODUCTION 1 1. Localized Chemical Bonding 3 1.A. Covalent Bonding 3 1.B. Multiple Valence 6 1.C. Hybridization 7 1.D. Multiple Bonds 9 1.E. Photoelectron Spectroscopy 11 1.F. Electronic Structures of Molecules 14 1.G. Electronegativity 15 1.H. Dipole Moment 18 1.I. Inductive and Field Effects 19 1.J. Bond Distances 21 1.K. Bond Angles 25 1.L. Bond Energies 27 2. Delocalized Chemical Bonding 31 2.A. Molecular Orbitals 32 2.B. Bond Energies and Distances in Compounds Containing Delocalized Bonds 35 2.C. Molecules that have Delocalized Bonds 37 2.D. Cross-Conjugation 42 2.E. The Rules of Resonance 43 2.F. The Resonance Effect 45 2.G. Steric Inhibition of Resonance and the Influences of Strain 46 2.H. pp-dp Bonding. Ylids 49 2.I. Aromaticity 50 2.J. Alternant and Nonalternant Hydrocarbons 63 2.K. Aromatic Systems with Electron Numbers other than Six 65 2.L. Other Aromatic Compounds 82 2.M. Hyperconjugation 85 2.N. Tautomerism 89 3. Bonding Weaker Than Covalent 96 3.A. Hydrogen Bonding 96 3.B. p-p Interactions 103 3.C. Addition Compounds 104 3.D. Catenanes and Rotaxanes 118 3.E. Cucurbit[n]Uril-Based Gyroscane 121 4. Stereochemistry and Conformation 122 4.A. Optical Activity and Chirality 122 4.B. What Kinds of Molecules Display Optical Activity? 125 4.C. The Fischer Projection 136 4.D. Absolute Configuration 137 4.E. The Cause of Optical Activity 145 4.F. Molecules with more than One Stereogenic Center 146 4.G. Asymmetric Synthesis 149 4.H. Methods of Resolution 154 4.I. Optical Purity 160 4.J. cis trans Isomerism 162 4.K. Out-In Isomerism 168 4.L. Enantiotopic and Diastereotopic Atoms, Groups, and Faces 170 4.M. Stereospecific and Stereoselective Syntheses 173 4.N. Conformational Analysis 173 4.O. Molecular Mechanics 190 4.P. STRAIN 192 5. Carbocations, Carbanions, Free Radicals, Carbenes, and Nitrenes 208 5.A. Carbocations 208 5.B. Carbanions 221 5.C. Free Radicals 234 5.D. Carbenes 249 5.E. Nitrenes 257 6. Mechanisms and Methods of Determining them 261 6.A. Types of Mechanism 261 6.B. Types of Reaction 262 6.C. Thermodynamic Requirements for Reaction 264 6.D. Kinetic Requirements for Reaction 266 6.E. The Baldwin Rules for Ring Closure 270 6.F. Kinetic and Thermodynamic Control 271 6.G. The Hammond Postulate 272 6.H. Microscopic Reversibility 273 6.I. Marcus Theory 273 6.J. Methods of Determining Mechanisms 275 7. Irradiation Processes in Organic Chemistry 289 7.A. Photochemistry 289 7.B. Sonochemistry 307 7.C. Microwave Chemistry 309 8. Acids and Bases 312 8.A. Bronsted Theory 312 8.B. The Mechanism of Proton-Transfer Reactions 323 8.C. Measurements of Solvent Acidity 324 8.D. Acid and Base Catalysis 327 8.E. Lewis Acids and Bases 330 8.F. The Effects of Structure on the Strengths of Acids and Bases 334 8.G. The Effects of the Medium on Acid and Base Strength 343 9. Effects of Structure and Medium on Reactivity 347 9.A. Resonance and Field Effects 347 9.B. Steric Effects 349 9.C. Quantitative Treatments of the Effect of Structure on Reactivity 352 9.D. Effect of Medium on Reactivity and Rate 361 PART II INTRODUCTION 367 10. Aliphatic Substitution, Nucleophilic and Organometallic 373 10.A. Mechanisms 373 10.B. SET Mechanisms 389 10.C. The Neighboring-Group Mechanism 391 10.D. The SNi Mechanism 408 10.E. Nucleophilic Substitution at an Allylic Carbon: Allylic Rearrangements 409 10.F. Nucleophilic Substitution at an Aliphatic Trigonal Carbon: The Tetrahedral Mechanism 413 10.G. Reactivity 417 10.H. Reactions 451 11. Aromatic Substitution, Electrophilic 569 11.A. Mechanisms 569 11.B. Orientation and Reactivity 576 11.C. Quantitative Treatments of Reactivity in the Substrate 586 11.D.A Quantitative Treatment of Reactivity of the Electrophile: The Selectivity Relationship 588 11.E. The Effect of the Leaving Group 591 11.F. Reactions 591 12. Aliphatic, Alkenyl, and Alkynyl Substitution, Electrophilic and Organometallic 649 12.A. Mechanisms 650 12.B. Reactivity 658 12.C. Reactions 660 13. Aromatic Substitution: Nucleophilic and Organometallic 732 13.A. Mechanisms 732 13.B. Reactivity 741 13.C. Reactions 745 14. Substitution Reactions: Radical 803 14.A. Mechanisms 803 14.B. Reactivity 812 14.C. Reactions 821 15. Addition to Carbon-Carbon Multiple Bonds 859 15.A. Mechanisms 859 15.B. Orientation and Reactivity 871 15.C. Reactions 881 16. Addition to Carbon-Hetero Multiple Bonds 1067 16.A. Mechanism and Reactivity 1067 16.B. Reactions 1075 17. Eliminations 1253 17.A. Mechanisms and Orientation 1253 17.B. Regiochemistry of the Double Bond 1269 17.C. Stereochemistry of the Double Bond 1273 17.D. Reactivity 1274 17.E. Mechanisms and Orientation in Pyrolytic Eliminations 1278 17.F. Reactions 1282 18. Rearrangements 1321 18.A. Mechanisms 1322 18.B. Longer Nucleophilic Rearrangements 1331 18.C. Free Radical Rearrangements 1333 18.D. Carbene Rearrangements 1337 18.E. Electrophilic Rearrangements 1337 18.F. Reactions 1337 19. Oxidations and Reductions 1433 19.A. Mechanisms 1434 19.B. Reactions 1436 APPENDIX A: THE LITERATURE OF ORGANIC CHEMISTRY 1569 APPENDIX B: CLASSIFICATION OF REACTIONS BY TYPE OF COMPOUNDS SYNTHESIZED 1605 INDEXES AUTHOR INDEX 1631 SUBJECT INDEX 1835.
  • (source: Nielsen Book Data)
The new, revised and updated 7th edition of March's Advanced Organic Chemistry clearly explains the theories and examples of organic chemistry, providing the most comprehensive resource about organic chemistry available. Readers are guided on planning and execution of multi-step synthetic reactions, with detailed descriptions of all the reactions. The first five chapters deal with the structure of organic compounds and discuss important organic chemistry bonds, fundamental principles of conformation, and stereochemistry of organic molecules, and reactive intermediates in organic chemistry. Chapters 6 to 9 are concerned with general principles of mechanism in organic chemistry, including acids and bases, photochemistry, sonochemistry and microwave irradiation, and finally the relationship between structure and reactivity. The last 10 chapters cover the nature and the scope of organic reactions and their mechanisms. The 7th edition proves again it is a must-have desktop reference and textbook for every student and professional working in organic chemistry or related fields. Key features of the 7th edition: * Every chapter has been updated with the most recent reaction information with references to both the primary and review literature * New to the 7th edition: 5,500 references since the last edition, updates / rewrites of the retained sections, and an updated index in Appendix B * Contains more than 1650 reactions and 20,000 valuable references to the primary literature * Includes appendices on the literature of organic chemistry and the classification of reactions according to the compounds synthesized * Guides the reader on planning and execution of multi-step synthetic reactions, with detailed descriptions of all the reactions. Reviews of the previous edition: "...a favorite general organic chemistry text and an easy-to-use one-volume reference. We are confident that this book will remain a dominant reference and that it will reside on many chemists' personal bookshelves." --Journal of Medicinal Chemistry "Who can hope to be seriously accepted as a member of the organic chemistry community without being in possession of at least one edition of 'March'?" --Chemistry and Industry.
(source: Nielsen Book Data)
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD251.2 .M37 2013 Unknown

18. Organic chemistry [2013]

Book
1 v. (various pagings) : ill. (some col.) ; 29 cm.
Acclaimed for its clarity and precision, Wade's Organic Chemistry maintains scientific rigor while engaging students at all levels. Wade presents a logical, systematic approach to understanding the principles of organic reactivity and the mechanisms of organic reactions. This approach helps students develop the problem-solving strategies and the scientific intuition they will apply throughout the course and in their future scientific work. The Eighth Edition provides enhanced and proven features in every chapter, including new Chapter Goals, Essential Problem-Solving Skills and Hints that encourage both majors and non-majors to think critically and avoid taking "short cuts" to solve problems. Mechanism Boxes and Key Mechanism Boxes strengthen student understanding of Organic Chemistry as a whole while contemporary applications reinforce the relevance of this science to the real world. This package contains:* Organic Chemistry, Eighth Edition.
(source: Nielsen Book Data)
Acclaimed for its clarity and precision, Wade's Organic Chemistry maintains scientific rigor while engaging students at all levels. Wade presents a logical, systematic approach to understanding the principles of organic reactivity and the mechanisms of organic reactions. This approach helps students develop the problem-solving strategies and the scientific intuition they will apply throughout the course and in their future scientific work. The Eighth Edition provides enhanced and proven features in every chapter, including new Chapter Goals, Essential Problem-Solving Skills and Hints that encourage both majors and non-majors to think critically and avoid taking "short cuts" to solve problems. Mechanism Boxes and Key Mechanism Boxes strengthen student understanding of Organic Chemistry as a whole while contemporary applications reinforce the relevance of this science to the real world. This package contains:* Organic Chemistry, Eighth Edition.
(source: Nielsen Book Data)
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD251.3 .W33 2013 Unknown
Book
xiii, 283 p. : ill ; 24 cm.
  • Introduction to Teaching Green Organic Chemistry Introduction Early Developments in Green Chemistry The Twelve Principles of Green Chemistry The Twelve Principles in Teaching Green Organic Chemistry Green Organic Chemistry Teaching Resources Conclusion References Designing a Green Organic Chemistry Lecture Course Introduction Challenges in Launching and Teaching a Green Chemistry Course Course Description and Structure Feedback Advice on Launching a Green Chemistry Course and Epilogue Instructive Lecture Case Studies References Elimination of Solvents in the Organic Curriculum Introduction Solvent-Free or Not Solvent-Free? Industrial and Academic Case Studies Solvent-free Reactor Design Eliminating Solvents in the Introductory Organic Laboratory Conclusion References Organic Reactions Under Aqueous Conditions Introduction Studies on the Origin of Enhanced Reactivity in Aqueous Conditions Aqueous Chemistry in the Undergraduate Organic Laboratory Lecture Case Studies in Aqueous Chemistry Conclusion References Organic Chemistry in Greener Non-Aqueous Media Introduction Measures of Solvent Greenness Supercritical Carbon Dioxide Fluorous Solvents Ionic Liquids Liquid Polymers Other Greener Solvents Future Outlook Conclusion References Environmentally-Friendly Organic Reagents Introduction Greener Reagents in the Undergraduate Organic Laboratory Conclusion References Organic Waste Management and Recycling Introduction Three Industrial Case Studies Reduction of Waste Generation Managing Generated Waste Reagent Recycling Recycling Solvents Recycling Consumer and Natural Products Conclusion References Greener Organic Reactions under Microwave Heating Introduction Microwave Heating as a Greener Technology Historical Background to Microwave Chemistry Microwave Versus Conventional Thermal Heating Solvents for Microwave Heating A Comparison of Multi-Mode and Mono-Mode Microwave Ovens Microwave-Accelerated Reactions for the Undergraduate Laboratory Literature Examples of Microwave-Accelerated Reactions Conclusion References Appendix: Greener Organic Chemistry Reaction Index.
  • (source: Nielsen Book Data)
The last decade has seen a huge interest in green organic chemistry, particularly as chemical educators look to "green" their undergraduate curricula. Detailing published laboratory experiments and proven case studies, this book discusses concrete examples of green organic chemistry teaching approaches from both lecture/seminar and practical perspectives. The experienced contributors address such topics as the elimination of solvents in the organic laboratory, organic reactions under aqueous conditions, organic reactions in non-aqueous media, greener organic reagents, waste management/recycling strategies, and microwave technology as a greener heating tool. This reference allows instructors to directly incorporate material presented in the text into their courses. Encouraging a stimulating organic chemistry experience, the text emphasizes the need for undergraduate education to: * Focus on teaching sustainability principles throughout the curriculum * Be flexible in the teaching of green chemistry, from modification of an existing laboratory experiment to development of a brand-new course * Reflect modern green research areas such as microwave reactivity, alternative reaction solvents, solvent-free chemistry, environmentally friendly reagents, and waste disposal * Train students in the "green chemistry decision-making" process Integrating recent research advances in green chemistry research and the Twelve Principles of Organic Chemistry into the lecture and laboratory environments, Green Organic Chemistry in Lecture and Laboratory highlights smaller, more cost-effective experiments with minimized waste disposal and reduced reaction times. This approach develops a fascinating and relevant undergraduate organic laboratory experience while focusing on real-world applications and problem-solving.
(source: Nielsen Book Data)
  • Introduction to Teaching Green Organic Chemistry Introduction Early Developments in Green Chemistry The Twelve Principles of Green Chemistry The Twelve Principles in Teaching Green Organic Chemistry Green Organic Chemistry Teaching Resources Conclusion References Designing a Green Organic Chemistry Lecture Course Introduction Challenges in Launching and Teaching a Green Chemistry Course Course Description and Structure Feedback Advice on Launching a Green Chemistry Course and Epilogue Instructive Lecture Case Studies References Elimination of Solvents in the Organic Curriculum Introduction Solvent-Free or Not Solvent-Free? Industrial and Academic Case Studies Solvent-free Reactor Design Eliminating Solvents in the Introductory Organic Laboratory Conclusion References Organic Reactions Under Aqueous Conditions Introduction Studies on the Origin of Enhanced Reactivity in Aqueous Conditions Aqueous Chemistry in the Undergraduate Organic Laboratory Lecture Case Studies in Aqueous Chemistry Conclusion References Organic Chemistry in Greener Non-Aqueous Media Introduction Measures of Solvent Greenness Supercritical Carbon Dioxide Fluorous Solvents Ionic Liquids Liquid Polymers Other Greener Solvents Future Outlook Conclusion References Environmentally-Friendly Organic Reagents Introduction Greener Reagents in the Undergraduate Organic Laboratory Conclusion References Organic Waste Management and Recycling Introduction Three Industrial Case Studies Reduction of Waste Generation Managing Generated Waste Reagent Recycling Recycling Solvents Recycling Consumer and Natural Products Conclusion References Greener Organic Reactions under Microwave Heating Introduction Microwave Heating as a Greener Technology Historical Background to Microwave Chemistry Microwave Versus Conventional Thermal Heating Solvents for Microwave Heating A Comparison of Multi-Mode and Mono-Mode Microwave Ovens Microwave-Accelerated Reactions for the Undergraduate Laboratory Literature Examples of Microwave-Accelerated Reactions Conclusion References Appendix: Greener Organic Chemistry Reaction Index.
  • (source: Nielsen Book Data)
The last decade has seen a huge interest in green organic chemistry, particularly as chemical educators look to "green" their undergraduate curricula. Detailing published laboratory experiments and proven case studies, this book discusses concrete examples of green organic chemistry teaching approaches from both lecture/seminar and practical perspectives. The experienced contributors address such topics as the elimination of solvents in the organic laboratory, organic reactions under aqueous conditions, organic reactions in non-aqueous media, greener organic reagents, waste management/recycling strategies, and microwave technology as a greener heating tool. This reference allows instructors to directly incorporate material presented in the text into their courses. Encouraging a stimulating organic chemistry experience, the text emphasizes the need for undergraduate education to: * Focus on teaching sustainability principles throughout the curriculum * Be flexible in the teaching of green chemistry, from modification of an existing laboratory experiment to development of a brand-new course * Reflect modern green research areas such as microwave reactivity, alternative reaction solvents, solvent-free chemistry, environmentally friendly reagents, and waste disposal * Train students in the "green chemistry decision-making" process Integrating recent research advances in green chemistry research and the Twelve Principles of Organic Chemistry into the lecture and laboratory environments, Green Organic Chemistry in Lecture and Laboratory highlights smaller, more cost-effective experiments with minimized waste disposal and reduced reaction times. This approach develops a fascinating and relevant undergraduate organic laboratory experience while focusing on real-world applications and problem-solving.
(source: Nielsen Book Data)
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
TP155.2 .E58 G765 2012 Unknown
Book
xviii, 340 p. : ill. ; 24 cm
"Providing advanced undergraduates and graduate students with a stepping stone from beginning level Organic Chemistry courses to organic synthesis research and/or graduate level coursework, Introduction to the Strategies of Organic Synthesis teaches the practical skills of making logical retrosynthetic disconnections, while reviewing basic organic transformations, reactions, and reactivities. The book is written to help undergraduates feel comfortable performing retrosynthetic analysis of a target molecule and subsequently develop more secure understanding of organic chemistry reactions overall"-- Provided by publisher.
"This book helps readers feel comfortable performing retrosynthetic analyses of target molecule synthesis and they will have a more secure understanding of organic chemistry reactions overall"-- Provided by publisher.
"Providing advanced undergraduates and graduate students with a stepping stone from beginning level Organic Chemistry courses to organic synthesis research and/or graduate level coursework, Introduction to the Strategies of Organic Synthesis teaches the practical skills of making logical retrosynthetic disconnections, while reviewing basic organic transformations, reactions, and reactivities. The book is written to help undergraduates feel comfortable performing retrosynthetic analysis of a target molecule and subsequently develop more secure understanding of organic chemistry reactions overall"-- Provided by publisher.
"This book helps readers feel comfortable performing retrosynthetic analyses of target molecule synthesis and they will have a more secure understanding of organic chemistry reactions overall"-- Provided by publisher.
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD262 .S815 2012 Unknown

Looking for different results?

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

Search elsewhere: Search WorldCat Search library website