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Book
xii, 149 pages : illustrations ; 25 cm
Chemistry & ChemEng Library (Swain)
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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.
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QD261 .L32 2014 Unknown
QD261 .L32 2014 Unknown
Book
xiv, 354 pages : illustrations ; 23 cm
  • Safety first, last, and always
  • Keeping a notebook
  • Interpreting a handbook
  • Jointware.
  • Safety first, last, and always
  • Keeping a notebook
  • Interpreting a handbook
  • Jointware.
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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

4. 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)
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QD253.2 .S65 2014 Unknown

5. Organic chemistry [2014]

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

6. 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

7. Organic chemistry [2014]

Book
1 v. (various pagings) : col. ill. ; 28 cm.
Chemistry & ChemEng Library (Swain)
Status of items at Chemistry & ChemEng Library (Swain)
Chemistry & ChemEng Library (Swain) Status
Stacks
QD251.3 .B78 2014 Unknown

8. Organic chemistry [2015]

Book
xxxvii, 1247 pages : illustrations (chiefly color) ; 29 cm
Chemistry & ChemEng Library (Swain)
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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)
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QD251.3 .O38 2014 Unknown
Book
(various pagings) : illustrations (some color) ; 29 cm
Chemistry & ChemEng Library (Swain)
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QD253.2 .K375 2014 Unknown
Book
x, 283 pages : illustrations (some color) ; 25 cm
Chemistry & ChemEng Library (Swain)
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QD476 .S54 2014 Unknown
Book
1 volume (various pagings) : illustrations ; 28 cm
Chemistry & ChemEng Library (Swain)
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Chemistry & ChemEng Library (Swain) Status
Permanent reserve
QD253.2 .S65 2014 Unknown
Book
vi, 950 pages : ill. ; 28 cm
Chemistry & ChemEng Library (Swain)
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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
  • Keeping records of laboratory work
  • Equipping the laboratory and the bench
  • Purification and drying of solvents
  • Reagents : preparation, purification, and handling
  • Gases
  • Vacuum pumps
  • Carrying out the reaction
  • Working up the reaction
  • Purification
  • Small-scale reactions
  • Large-scale reactions
  • Special procedures
  • Characterization
  • Troubleshooting : what to do when things don't work
  • The chemical literature
  • Appendix 1. Properties of common solvents
  • Appendix 2. Properties of common gases
  • Appendix 3. Approximate pKa values for some common reagents versus common bases
  • Appendix 4. Common Bronsted acids
  • Appendix 5. Common Lewis acids
  • Appendix 6. Common reducing reagents
  • Appendix 7. Common oxidizing reagents.
  • General introduction
  • Safety
  • Keeping records of laboratory work
  • Equipping the laboratory and the bench
  • Purification and drying of solvents
  • Reagents : preparation, purification, and handling
  • Gases
  • Vacuum pumps
  • Carrying out the reaction
  • Working up the reaction
  • Purification
  • Small-scale reactions
  • Large-scale reactions
  • Special procedures
  • Characterization
  • Troubleshooting : what to do when things don't work
  • The chemical literature
  • Appendix 1. Properties of common solvents
  • Appendix 2. Properties of common gases
  • Appendix 3. Approximate pKa values for some common reagents versus common bases
  • Appendix 4. Common Bronsted acids
  • Appendix 5. Common Lewis acids
  • Appendix 6. Common reducing reagents
  • Appendix 7. Common oxidizing reagents.
Chemistry & ChemEng Library (Swain)
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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)
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QD251.3 .S38 2013 Unknown
Book
xxv, 2047 pages : illustrations ; 26 cm
  • Localized chemical bonding
  • Delocalized chemical bonding
  • Bonding weaker than covalent
  • Stereochemistry and conformation
  • Carbocations, carbanions, free radicals, carbenes, and nitrenes
  • Mechanisms and methods of determining them
  • Irradiation processes in organic chemistry
  • Acids and bases
  • Effects of structure and medium on reactivity
  • Aliphatic substitution, nucleophilic and organometallic
  • Aromatic substitution, electrophilic
  • Aliphatic, alkenyl, and alkynyl substitution, electrophilic and organometallic
  • Aromatic substitution, nucleophilic and organometallic
  • Substitution reactions, radical
  • Addition to carbon-carbon multiple bonds
  • Addition to carbon-hetero multiple bonds
  • Eliminations
  • Rearrangements
  • Oxidations and reductions
  • Appendix A. The literature of organic chemistry
  • Appendix B. Classification of reactions by type of compounds synthesized.
  • Localized chemical bonding
  • Delocalized chemical bonding
  • Bonding weaker than covalent
  • Stereochemistry and conformation
  • Carbocations, carbanions, free radicals, carbenes, and nitrenes
  • Mechanisms and methods of determining them
  • Irradiation processes in organic chemistry
  • Acids and bases
  • Effects of structure and medium on reactivity
  • Aliphatic substitution, nucleophilic and organometallic
  • Aromatic substitution, electrophilic
  • Aliphatic, alkenyl, and alkynyl substitution, electrophilic and organometallic
  • Aromatic substitution, nucleophilic and organometallic
  • Substitution reactions, radical
  • Addition to carbon-carbon multiple bonds
  • Addition to carbon-hetero multiple bonds
  • Eliminations
  • Rearrangements
  • Oxidations and reductions
  • Appendix A. The literature of organic chemistry
  • Appendix B. Classification of reactions by type of compounds synthesized.
Chemistry & ChemEng Library (Swain)
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QD251.2 .M37 2013 Unknown

17. 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)
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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)
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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)
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QD262 .S815 2012 Unknown

20. Organic chemistry [2012]

Book
1 v. (various pagings) : col. ill. ; 26 cm.
Chemistry & ChemEng Library (Swain)
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Chemistry & ChemEng Library (Swain) Status
Request at circulation desk
QD251.3 .M364 2012 Unknown On Reserve 2-hour loan
CHEM-131-01, CHEM-131-01, CHEM-33-01, CHEM-33-01
Course
CHEM-131-01 -- Organic Polyfunctional Compounds
Instructor(s)
Huestis, Wray H
Course
CHEM-131-01 -- Organic Polyfunctional Compounds
Instructor(s)
Xia, Yan
Course
CHEM-33-01 -- Structure and Reactivity
Instructor(s)
Kanan, Matthew W.
Course
CHEM-33-01 -- Structure and Reactivity
Instructor(s)
McClory, Megan Kathleen

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