{"product_id":"understanding-organic-chemistry-bridging-fundamental-and-advanced-courses-hardback-9781394179831","title":"Understanding Organic Chemistry; Bridging Fundamental and Advanced Courses (Hardback) 9781394179831","description":"\u003cfont face=\"Georgia\"\u003e\r\n\u003cp\u003e\u003cfont size=\"6\"\u003eUnderstanding Organic Chemistry\u003c\/font\u003e\u003cbr\u003e\r\n\u003cfont size=\"5\"\u003eBridging Fundamental and Advanced Courses\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\r\n\r\n\u003cp\u003e\u003cfont size=\"4\"\u003eAnn M. Fabirkiewicz (Author), John C. Stowell (Author)\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e9781394179831, Wiley\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eHardback, published 1 October 2025\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e448 pages\u003cbr\u003e23.6 x 15.8 x 4.1 cm, 0.703 kg\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\r\n\r\n\r\n\u003cp align=\"justify\"\u003e\u003cstrong\u003e\u003cfont size=\"3\"\u003e\u003cp\u003e\u003cb\u003eProvides a clear and cohesive path from fundamentals to advanced organic chemistry\u003c\/b\u003e \u003c\/p\u003e\n\u003cp\u003e\u003ci\u003eUnderstanding Organic Chemistry: Bridging Fundamental and Advanced Courses\u003c\/i\u003e equips students with the conceptual tools and technical knowledge needed to transition confidently from lower-division coursework to upper-level study and research in organic chemistry. By integrating synthetic and physical organic chemistry, this popular textbook helps students understand reaction mechanisms, stereochemical principles, and synthetic strategies in a way that is both rigorous and accessible. \u003c\/p\u003e\n\u003cp\u003eThe new fourth edition continues its dual focus on theoretical grounding and hands-on problem-solving, making it ideal for those who want to deepen their command of the subject and begin reading primary research literature with confidence. The text incorporates substantial updates throughout, including contemporary examples from synthetic chemistry, enhanced coverage of chiral catalysts and ene reactions, and newly developed in-text problem sets designed to promote self-guided learning. The chapters are structured around major themes—such as spectroscopy, reaction mechanisms, and functional group transformations—and include clear, concise explanations followed by extensive end-of-chapter exercises. Select problem answers are now available in the text, with full solutions and teaching materials accessible to instructors through a companion website. \u003c\/p\u003e\n\u003cp\u003eA balanced treatment of synthetic and physical organic chemistry that promotes a deeper conceptual understanding of the subject, \u003ci\u003eUnderstanding Organic Chemistry:\u003c\/i\u003e \u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eIntroduces modern synthetic topics and recent advances in bond-forming methodologies\u003c\/li\u003e\n\u003cli\u003eProvides up-to-date coverage of spectroscopy, functional group transformations, and synthesis design\u003c\/li\u003e\n\u003cli\u003eExplains stereochemistry and reaction mechanisms in a clear, structured manner ideal for advanced learners\u003c\/li\u003e\n\u003cli\u003eEnables students to critically engage with primary research literature in organic chemistry\u003c\/li\u003e\n\u003c\/ul\u003e \u003cp\u003eWith a student-friendly format that supports both coursework and self-directed study, \u003ci\u003eUnderstanding Organic Chemistry: Bridging Fundamental and Advanced Courses, Fourth Edition,\u003c\/i\u003e is ideal for junior- and senior-level undergraduates as well as first-year graduate students enrolled in intermediate or advanced organic chemistry courses. It is also a valuable reference for chemistry majors preparing for careers or further study in pharmaceuticals, materials science, or academic research.\u003c\/p\u003e\u003c\/font\u003e\u003c\/strong\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e\u003cp\u003ePreface to the Fourth Edition xi\u003c\/p\u003e \u003cp\u003ePreface to the Third Edition xiii\u003c\/p\u003e \u003cp\u003ePreface to the Second Edition xv\u003c\/p\u003e \u003cp\u003ePreface to the First Edition xvii\u003c\/p\u003e \u003cp\u003eAbout the Companion Website xix\u003c\/p\u003e \u003cp\u003e\u003cb\u003e1 Reading Nomenclature 1\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1.1 Acyclic Polyfunctional Molecules 2\u003c\/p\u003e \u003cp\u003e1.2 Monocyclic Aliphatic Compounds 3\u003c\/p\u003e \u003cp\u003e1.3 Bridged Polycyclic Structures 4\u003c\/p\u003e \u003cp\u003e1.4 Fused Polycyclic Compounds 6\u003c\/p\u003e \u003cp\u003e1.5 Spiro Compounds 10\u003c\/p\u003e \u003cp\u003e1.6 Monocyclic Heterocyclic Compounds 11\u003c\/p\u003e \u003cp\u003e1.7 Fused-Ring Heterocyclic Compounds 16\u003c\/p\u003e \u003cp\u003e1.8 Bridged and Spiro Heterocyclic Compounds 19\u003c\/p\u003e \u003cp\u003eResources 20\u003c\/p\u003e \u003cp\u003eProblems 21\u003c\/p\u003e \u003cp\u003eReferences 22\u003c\/p\u003e \u003cp\u003e\u003cb\u003e2 Accessing Chemical Information 25\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e2.1 Databases 25\u003c\/p\u003e \u003cp\u003e2.2 Chemical Literature 26\u003c\/p\u003e \u003cp\u003e2.3 Synthetic Procedures 28\u003c\/p\u003e \u003cp\u003e2.4 Health and Safety Information 29\u003c\/p\u003e \u003cp\u003eProblems 32\u003c\/p\u003e \u003cp\u003eReferences 34\u003c\/p\u003e \u003cp\u003e\u003cb\u003e3 Stereochemistry 37\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e3.1 Representations 37\u003c\/p\u003e \u003cp\u003e3.2 Vocabulary 39\u003c\/p\u003e \u003cp\u003e3.3 Property Differences Among Stereoisomers 42\u003c\/p\u003e \u003cp\u003e3.4 Resolution of Enantiomers 46\u003c\/p\u003e \u003cp\u003e3.5 Enantioselective Synthesis 49\u003c\/p\u003e \u003cp\u003e3.5.1 Chiral Templates 50\u003c\/p\u003e \u003cp\u003e3.5.2 Chiral Catalysts 50\u003c\/p\u003e \u003cp\u003e3.5.3 Chiral Reagents 51\u003c\/p\u003e \u003cp\u003e3.5.4 Substrate-Directed Enantioselective Reactions 52\u003c\/p\u003e \u003cp\u003e3.6 Reactions at a Stereogenic Atom 53\u003c\/p\u003e \u003cp\u003e3.6.1 Racemization 53\u003c\/p\u003e \u003cp\u003e3.6.2 Epimerization 53\u003c\/p\u003e \u003cp\u003e3.6.3 Inversion 54\u003c\/p\u003e \u003cp\u003e3.6.4 Retention 55\u003c\/p\u003e \u003cp\u003e3.6.5 Transfer 56\u003c\/p\u003e \u003cp\u003e3.7 Relative and Absolute Configurations 57\u003c\/p\u003e \u003cp\u003e3.8 Topism 59\u003c\/p\u003e \u003cp\u003eResources 63\u003c\/p\u003e \u003cp\u003eProblems 63\u003c\/p\u003e \u003cp\u003eReferences 70\u003c\/p\u003e \u003cp\u003e\u003cb\u003e4 Mechanisms and Predictions 75\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e4.1 Reaction Coordinate Diagrams and Mechanisms 75\u003c\/p\u003e \u003cp\u003e4.2 The Hammond Postulate 77\u003c\/p\u003e \u003cp\u003e4.3 Methods for Determining Mechanisms 78\u003c\/p\u003e \u003cp\u003e4.3.1 Identification of Products and Intermediates 78\u003c\/p\u003e \u003cp\u003e4.3.2 Isotope Tracing 78\u003c\/p\u003e \u003cp\u003e4.3.3 Stereochemical Determination 79\u003c\/p\u003e \u003cp\u003e4.3.4 Concentration Dependence of Kinetics 81\u003c\/p\u003e \u003cp\u003e4.3.5 Isotope Effects in Kinetics 90\u003c\/p\u003e \u003cp\u003e4.3.6 Temperature Effects on Kinetics 92\u003c\/p\u003e \u003cp\u003e4.3.7 Substituent Effects on Kinetics 94\u003c\/p\u003e \u003cp\u003e4.4 Worked Examples 100\u003c\/p\u003e \u003cp\u003e4.4.1 Reactions in Basic Solutions 100\u003c\/p\u003e \u003cp\u003e4.4.2 Reactions in Acidic Solutions 104\u003c\/p\u003e \u003cp\u003e4.4.3 Free Radical Reactions 108\u003c\/p\u003e \u003cp\u003e4.4.4 Molecular Rearrangements 111\u003c\/p\u003e \u003cp\u003eResource 113\u003c\/p\u003e \u003cp\u003eProblems 114\u003c\/p\u003e \u003cp\u003eReferences 126\u003c\/p\u003e \u003cp\u003e\u003cb\u003e5 Electron Delocalization Aromatic Character and Pericyclic Reactions 129\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e5.1 Molecular Orbitals 130\u003c\/p\u003e \u003cp\u003e5.2 Aromatic Character 136\u003c\/p\u003e \u003cp\u003e5.3 Pericyclic Reactions 141\u003c\/p\u003e \u003cp\u003e5.3.1 Cycloaddition Reactions 143\u003c\/p\u003e \u003cp\u003e5.3.2 Electrocyclic Reactions 148\u003c\/p\u003e \u003cp\u003e5.3.3 Sigmatropic Reactions 153\u003c\/p\u003e \u003cp\u003e5.3.4 Ene Reactions 156\u003c\/p\u003e \u003cp\u003e5.3.5 Selection Rules for Pericyclic Reactions 158\u003c\/p\u003e \u003cp\u003eResources 159\u003c\/p\u003e \u003cp\u003eProblems 159\u003c\/p\u003e \u003cp\u003eReferences 167\u003c\/p\u003e \u003cp\u003e\u003cb\u003e6 Functional Group Transformations 171\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e6.1 Carboxylic Acids and Related Derivatives 172\u003c\/p\u003e \u003cp\u003e6.1.1 Carboxylic Acids 172\u003c\/p\u003e \u003cp\u003e6.1.2 Carboxylic Esters 174\u003c\/p\u003e \u003cp\u003e6.1.3 Carboxylic Amides 176\u003c\/p\u003e \u003cp\u003e6.1.4 Carboxylic Acid Halides 176\u003c\/p\u003e \u003cp\u003e6.1.5 Carboxylic Anhydrides 176\u003c\/p\u003e \u003cp\u003e6.1.6 Nitriles 177\u003c\/p\u003e \u003cp\u003e6.1.7 Ortho Esters 178\u003c\/p\u003e \u003cp\u003e6.2 Aldehydes Ketones and Derivatives 179\u003c\/p\u003e \u003cp\u003e6.2.1 Aldehydes 179\u003c\/p\u003e \u003cp\u003e6.2.2 Ketones 182\u003c\/p\u003e \u003cp\u003e6.2.3 Imines and Enamines 182\u003c\/p\u003e \u003cp\u003e6.2.4 Acetals 183\u003c\/p\u003e \u003cp\u003e6.2.5 Vinyl Ethers 185\u003c\/p\u003e \u003cp\u003e6.3 Alcohols 186\u003c\/p\u003e \u003cp\u003e6.4 Ethers 187\u003c\/p\u003e \u003cp\u003e6.5 Alkyl Halides 189\u003c\/p\u003e \u003cp\u003e6.5.1 Alkyl Chlorides and Alkyl Bromides 190\u003c\/p\u003e \u003cp\u003e6.5.2 Alkyl Iodides 192\u003c\/p\u003e \u003cp\u003e6.5.3 Alkyl Fluorides 192\u003c\/p\u003e \u003cp\u003e6.6 Amines 194\u003c\/p\u003e \u003cp\u003e6.7 Isocyanates 195\u003c\/p\u003e \u003cp\u003e6.8 Alkenes 195\u003c\/p\u003e \u003cp\u003e6.9 Reductive Removal of Functionality 198\u003c\/p\u003e \u003cp\u003eResources 199\u003c\/p\u003e \u003cp\u003eProblems 199\u003c\/p\u003e \u003cp\u003eReferences 206\u003c\/p\u003e \u003cp\u003e\u003cb\u003e7 Carbon–Carbon Bond Formation 213\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e7.1 Carbon–Carbon Single-Bond Formation 214\u003c\/p\u003e \u003cp\u003e7.1.1 Reactions in Basic Solutions 214\u003c\/p\u003e \u003cp\u003e7.1.2 Reactions in Acidic Solutions 221\u003c\/p\u003e \u003cp\u003e7.1.3 Organometallic Coupling Reactions 224\u003c\/p\u003e \u003cp\u003e7.2 Carbon–Carbon Double-Bond Formation 226\u003c\/p\u003e \u003cp\u003e7.3 Multibond Processes 229\u003c\/p\u003e \u003cp\u003eResources 231\u003c\/p\u003e \u003cp\u003eProblems 232\u003c\/p\u003e \u003cp\u003eReferences 238\u003c\/p\u003e \u003cp\u003e\u003cb\u003e8 Planning Multistep Syntheses 243\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e8.1 Retrosynthetic Analysis 243\u003c\/p\u003e \u003cp\u003e8.2 Disconnection at a Functional Group or a Branch Point 244\u003c\/p\u003e \u003cp\u003e8.3 Cooperation for Difunctionality 248\u003c\/p\u003e \u003cp\u003e8.4 Ring Closure 258\u003c\/p\u003e \u003cp\u003e8.5 Acetylide Alkylation and Addition 262\u003c\/p\u003e \u003cp\u003e8.6 The Diels–Alder Reaction 264\u003c\/p\u003e \u003cp\u003e8.7 The Claisen Rearrangement 268\u003c\/p\u003e \u003cp\u003e8.8 Asymmetric Synthesis 272\u003c\/p\u003e \u003cp\u003e8.9 Synthetic Strategies 273\u003c\/p\u003e \u003cp\u003e8.10 Final Note 276\u003c\/p\u003e \u003cp\u003eResources 276\u003c\/p\u003e \u003cp\u003eProblems 277\u003c\/p\u003e \u003cp\u003eReferences 282\u003c\/p\u003e \u003cp\u003e\u003cb\u003e9 Physical Influences on Reactions 289\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e9.1 Unimolecular Reactions 290\u003c\/p\u003e \u003cp\u003e9.2 Homogeneous Two-Component Reactions 291\u003c\/p\u003e \u003cp\u003e9.3 Temperature Effects 292\u003c\/p\u003e \u003cp\u003e9.4 Pressure Effects 294\u003c\/p\u003e \u003cp\u003e9.5 Solvent Effects 295\u003c\/p\u003e \u003cp\u003e9.6 Biphasic Reactions 296\u003c\/p\u003e \u003cp\u003e9.6.1 Phase-Transfer Catalysis 296\u003c\/p\u003e \u003cp\u003e9.6.2 Increasing Solubility 299\u003c\/p\u003e \u003cp\u003e9.6.3 Increasing Surface Area 299\u003c\/p\u003e \u003cp\u003e9.6.4 Flow Chemistry 300\u003c\/p\u003e \u003cp\u003e9.6.5 Ultrasound 301\u003c\/p\u003e \u003cp\u003e9.7 Reactions on Chemical Supports 302\u003c\/p\u003e \u003cp\u003e9.8 Using Unfavorable Equilibria 305\u003c\/p\u003e \u003cp\u003e9.9 Green Chemistry 307\u003c\/p\u003e \u003cp\u003eResources 308\u003c\/p\u003e \u003cp\u003eProblems 309\u003c\/p\u003e \u003cp\u003eReferences 312\u003c\/p\u003e \u003cp\u003e\u003cb\u003e10 Survey of Organic Spectroscopy 317\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e10.1 Electromagnetic Radiation 317\u003c\/p\u003e \u003cp\u003e10.2 Ultraviolet Spectroscopy 319\u003c\/p\u003e \u003cp\u003e10.2.1 Origin of the Signals 319\u003c\/p\u003e \u003cp\u003e10.2.2 Interpretation 320\u003c\/p\u003e \u003cp\u003e10.2.3 Visible Spectroscopy 320\u003c\/p\u003e \u003cp\u003e10.3 Infrared Spectroscopy 322\u003c\/p\u003e \u003cp\u003e10.3.1 Origin of the Signals 322\u003c\/p\u003e \u003cp\u003e10.3.2 Interpretation 322\u003c\/p\u003e \u003cp\u003e10.4 Mass Spectrometry 324\u003c\/p\u003e \u003cp\u003e10.4.1 Origin of the Signals 324\u003c\/p\u003e \u003cp\u003e10.4.2 Interpretation 325\u003c\/p\u003e \u003cp\u003e10.5 NMR Spectroscopy 326\u003c\/p\u003e \u003cp\u003e10.5.1 Origin of the Signals 327\u003c\/p\u003e \u003cp\u003e10.5.2 Interpretation of Proton NMR Spectra 330\u003c\/p\u003e \u003cp\u003e10.6 Carbon NMR Spectra 342\u003c\/p\u003e \u003cp\u003e10.6.1 General Characteristics 343\u003c\/p\u003e \u003cp\u003e10.6.2 Interpretation of 13C NMR Spectra 345\u003c\/p\u003e \u003cp\u003e10.7 Correlation of 1H and 13C NMR Spectra 348\u003c\/p\u003e \u003cp\u003eResources 350\u003c\/p\u003e \u003cp\u003eProblems 350\u003c\/p\u003e \u003cp\u003eReferences 357\u003c\/p\u003e \u003cp\u003eAppendix A Common Chemical Abbreviations 359\u003c\/p\u003e \u003cp\u003eAppendix B Common Protecting Groups 365\u003c\/p\u003e \u003cp\u003eAppendix C Answers to Selected Problems 371\u003c\/p\u003e \u003cp\u003eIndex 415\u003c\/p\u003e\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eSubject Areas: Chemistry [\u003ca title=\"See our other books on Chemistry\" href=\"https:\/\/freshlyprintedbooks.co.uk\/search?q=%22Chemistry%20%5BPN%5D%22\"\u003ePN\u003c\/a\u003e]\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\u003c\/font\u003e","brand":"Wiley","offers":[{"title":"Brand New","offer_id":52433192026392,"sku":"9781394179831","price":81.99,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0730\/2037\/5320\/files\/9781394179831.jpg?v=1784851294","url":"https:\/\/freshlyprintedbooks.co.uk\/products\/understanding-organic-chemistry-bridging-fundamental-and-advanced-courses-hardback-9781394179831","provider":"Freshly Printed Books","version":"1.0","type":"link"}