Organic Chemistry, 13th Edition
By Graham Solomons, Craig Fryhle, and Scott Snyder
Organic Chemistry prepares students for success in the organic classroom and beyond by emphasizing the relationship between structure and reactivity. To accomplish this, the content is organized in a way that combines the most useful features of a functional group approach with one largely based on reaction mechanisms. The authors’ philosophy is to emphasize mechanisms and their common aspects as often as possible, and at the same time use the unifying features of functional groups as the basis for most sections. The structural aspects show students what organic chemistry is and mechanistic aspects show students how it works. And wherever an opportunity arises, the authors show students what organic chemistry does in living systems and the physical world around us.
WileyPLUS for Organic Chemistry strikes the perfect balance between theory and practice with a combination of interactive concept maps, mechanism and reaction explorer practice, and video walkthroughs. Through an interactive approach, students learn how to put the pieces of organic chemistry together to solve problems. The Solomons tried-and-true pedagogy has helped students from North America and around the world develop proficiency in the key skills they need to succeed. And this new edition engages your students in one of the most up-to-date organic chemistry titles available.
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Concept and Mechanism Lightboard Videos
The 13th edition includes new author-built lightboard videos covering topics on mechanisms, synthesis pathways, and everyday relations of chemistry in our lives.
Interactive Concept Maps
Interactive Concept Maps allow students to test their knowledge of synthetic connections and summaries of reactions by actively engaging with the material through a series of interactive exercises.
Step-by-Step Mechanism Walkthrough Videos
Walkthrough Videos review the mechanisms presented in each section, giving students extra visual guidance to help them master concepts.
Solved Problem Videos
Solved Problem Videos demonstrate effective problem-solving strategies by walking students through problems using audio and a whiteboard.
Instructor Resources
- Test Bank contains more than 3,000 questions, including multiple-choice, true-false, short answer, fill in the blank and critical thinking problems. A full computerized version is also available with full editing to customize tests.
- New TestGen computerized test bank allows for quick creation of quizzes or tests. TestGen provides a variety of question types and allows instructors to create their own questions.
- Digital Image Archive text website includes downloadable files of text images in JPEG format.
- PowerPoint Lecture Slides highlight key concepts and contain numerous clicker questions and include examples and illustrations. Includes images from the text.
- PowerPoint Slides with Text Images
- Personal Response Systems “Clicker” Questions
Additional Features Include
- Video Mini-Lectures: These videos focus on explaining challenging concepts from each chapter. They are ideal for flipped/hybrid classes or as a supplement to traditional lectures.
- Reaction, Mechanism, and Synthesis Explorers: Using Reaction Explorer, students complete reactions and get the necessary drill-and-practice to learn the correct steps along the way.
- Guided Online Tutorials: A subset of end of chapter problems are linked out to stepped-out problem-solving tutorials that walk student through the problems with individualized feedback at each step.
- Pre-Lecture Assignments: Pre-loaded and ready to use, these assignments are carefully designed to assess students prior to class. Instructors can assign these pre-created quizzes to gauge student preparedness prior to lecture and tailor class time based on the scores and participation.
- Skill Building Exercises: Animated exercises with instant feedback to reinforce the key skills needed to succeed in organic chemistry.
- 90+% of review problems and end of chapter questions are coded for online assessment. Many are algorithmic and feature structure drawing/assessment functionality using MarvinSketch with immediate answer feedback and video question assistance.
T.W. Graham Solomons completed his undergraduate work at The Citadel and received his doctorate in organic chemistry in 1959 from Duke University where he worked with C.K. Bradsher. Following this he was a Sloan Foundation Postdoctoral Fellow at the University of Rochester where he worked with V. Boekelheide. In 1960 he became a charter member of the faculty of the University of South Florida and became Professor of Chemistry in 1973. In 1992 he was made Professor Emeritus. His Research interests are in areas of heterocyclic chemistry and unusual aromatic compounds. He has published papers in The Journal of the American Chemical Society, the Journal of Organic Chemistry, and the Journal of Heterocyclic Chemistry. He has received several awards for distinguished teaching. .
Craig B. Fryhle is Chair and Professor of Chemistry at Pacific Lutheran University. He earned his B.A. degree from Gettysburg College and Ph.D. from Brown University. His experiences at these institutions shaped his dedication to mentoring undergraduate students in chemistry and the liberal arts – a passion for him. His research interests have been in areas relating to the shikimic acid pathway, including molecular modeling and NMR spectrometry of substrates and analogues, as well as structure and reactivity studies of Shikimate pathways enzymes using isotopic labeling and mass spectrometry.
Scott A. Snyder grew up in the suburbs of Buffalo, NY and graduated from Williams College summa cum laude in 1999. He pursued his doctoral studies at The Scripps Research Institute in La Jolla, CA under the tutelage of K. C. Nicolaou as an NSF, Pfizer, and Bristol-Myers Squibb predoctoral fellow. While there, he co-authored the graduate textbook Classics in Total Synthesis II with his doctoral mentor. Scott was then an NIH postdoctoral fellow with E. J. Corey at Harvard University. In 2006, Scott began his independent career at Columbia University, moved to The Scripps Research Institute on their Jupiter FL campus in 2013, and in 2015 assumed his current position as Professor of Chemistry at the University of Chicago. His research interests are in natural products total synthesis, particularly unique polyphenols, alkaloids, and halogenated materials. He has trained more than 60 students at the high school, undergraduate, graduate, and postdoctoral levels and co-authored more than 50 research and review articles. Scott has received a number of awards and honors, including a Camille and Henry Dreyfus New Faculty Award, an Amgen Young Investigator Award, an Eli Lilly Grantee Award, a Bristol-Myers Squibb Unrestricted Grant Award, an Alfred P. Sloan Foundation Fellowship, a DuPont Young Professor Award, and an Arthur C. Cope Scholar Award from the American Chemical Society. He has also received awards recognizing his teaching, including a Cottrell Scholar Award from the Research Corporation for Science Advancement. He lives in Chicago with his wife Cathy and son Sebastian where he enjoys gardening, cooking, cycling, and watching movies.
1. The Basics: Bonding and Molecular Structure
2. Families of Carbon Compounds: Functional Groups, Intermolecular Forces, and Infrared (IR) Spectroscopy
3. Acids and Bases: An Introduction to Organic Reactions and Their Mechanisms
4. Nomenclature and Conformations of Alkanes and Cycloalkanes
5. Stereochemistry: Chiral Molecules
6. Nucleophilic Reactions: Properties and Substitution Reactions of Alkyl Halides
7. Alkenes and Alkynes I: Properties and Synthesis. Elimination Reactions of Alkyl Halides
8. Alkenes and Alkynes II: Addition Reactions
9. Nuclear Magnetic Resonance and Mass Spectrometry: Tools for Structure Determination
10. Radical Reactions
11. Alcohols and Ethers: Synthesis and Reactions
12. Alcohols from Carbonyl Compounds: Oxidation Reduction and Organometallic Compounds
13. Conjugated Unsaturated Systems
14. Aromatic Compounds
15. Reactions of Aromatic Compounds
16. Aldehydes and Ketones: Nucleophilic Addition to the Carbonyl Group
17. Carboxylic Acids and Their Derivatives: Nucleophilic Addition-Elimination at the Acyl Carbon
18. Reactions at the α Carbon of Carbonyl Compounds: Enols and Enolates
19. Condensation and Conjugate Addition Reactions of Carbonyl Compounds: More Chemistry of Enolates
20. Amines
21. Transition Metal Complexes: Promoters of Key Bond Forming Reactions
22. Carbohydrates
23. Lipids
24. Amino Acids and Proteins
25. Nucleic Acids and Protein Synthesis