Organic Chemistry: 100 Must-Know Mechanisms
eBook - ePub

Organic Chemistry: 100 Must-Know Mechanisms

  1. 289 pages
  2. English
  3. ePUB (mobile friendly)
  4. Available on iOS & Android
eBook - ePub

Organic Chemistry: 100 Must-Know Mechanisms

About this book

In chemistry, good problem-solving requires a balanced combination of scientific intuition and
methodical analysis. Additionally, thoughtfully presented diagrams and infographics can convey
a large amount of complex information in a more intuitive and accessible manner. 100 Must-Know
Mechanisms (Second Edition) strives to be at the intersection of these two key principles. Its
thorough visualizations enable experienced readers to use it as a quick reference for specific
mechanisms of interest. At the same time, the book's breadth of covered reactions, from classic to
cutting-edge, make it a good study-aid for the developing chemist. A slow and consistent study of
the entire series of mechanisms can help set the foundation for good scientific intuition, while its
detailed infographics and careful navigation features encourage coming back to it frequently. This
edition includes over 40 new illustrations, numerous new mechanistic schemes, enhanced original
figures with a variety of real-case examples, and more

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Yes, you can access Organic Chemistry: 100 Must-Know Mechanisms by Roman Valiulin in PDF and/or ePUB format, as well as other popular books in Physical Sciences & Physical & Theoretical Chemistry. We have over one million books available in our catalogue for you to explore.

Information

Table of contents

  1. Title Page
  2. Copyright
  3. Contents
  4. Second Edition
  5. List of Acronyms and Abbreviations
  6. 1 Electrophilic Addition Mechanism
  7. 2 Nucleophilic Substitution Mechanism
  8. 3 Aromatic Electrophilic Substitution Mechanism
  9. 4 Aromatic Nucleophilic Substitution Mechanism
  10. 5 Aromatic Radical Nucleophilic Substitution Mechanism
  11. 6 Elimination Mechanism
  12. 7 Acyloin Condensation
  13. 8 Alkyne Zipper Reaction
  14. 9 Arbuzov Reaction
  15. 10 Arndt–Eistert Synthesis
  16. 11 Baeyer–Villiger Oxidation
  17. 12 Barton Decarboxylation
  18. 13 Baylis–Hillman Reaction
  19. 14 Beckmann Rearrangement
  20. 15 Benzoin Condensation
  21. 16 Benzyne Mechanism
  22. 17 Bergman Cyclization
  23. 18 Birch Reduction
  24. 19 Bischler‒Napieralski Cyclization
  25. 20 Brown Hydroboration
  26. 21 Buchwald–Hartwig Cross-Coupling
  27. 22 Cannizzaro Reaction
  28. 23 Chan–Evans–Lam Cross-Coupling
  29. 24 Chichibabin Amination
  30. 25 Claisen Condensation
  31. 26 Claisen Rearrangement
  32. 27 Cope Elimination
  33. 28 Cope Rearrangement
  34. 29 Criegee and Malaprade Oxidation
  35. 30 CuAAC
  36. 31 Curtius Rearrangement
  37. 32 Darzens Condensation
  38. 33 Dess–Martin Oxidation
  39. 34 Diazotization (Diazonium Salt)
  40. 35 Diels–Alder Cycloaddition
  41. 36 Di-π-Methane Rearrangement
  42. 37 Favorskii Rearrangement
  43. 38 Fischer Indole Synthesis
  44. 39 Friedel–Crafts Acylation and Alkylation
  45. 40 Gabriel Synthesis
  46. 41 Gewald Reaction
  47. 42 Glaser–Eglinton–Hay Coupling
  48. 43 Grignard Reaction
  49. 44 Grob Fragmentation
  50. 45 Haloform Reaction
  51. 46 Heck Cross-Coupling
  52. 47 Hell–Volhard–Zelinsky Reaction
  53. 48 Hiyama Cross-Coupling
  54. 49 Hofmann Elimination
  55. 50 Horner–Wadsworth–Emmons Olefination
  56. 51 Jones Oxidation
  57. 52 Kucherov Reaction
  58. 53 Kumada Cross-Coupling
  59. 54 Ley–Griffith Oxidation
  60. 55 Liebeskind–Srogl Cross-Coupling
  61. 56 Mannich Reaction
  62. 57 McMurry Coupling
  63. 58 Meerwein–Ponndorf–Verley Reduction
  64. 59 Michael Addition
  65. 60 Minisci Reaction
  66. 61 Mitsunobu Reaction
  67. 62 Miyaura Borylation
  68. 63 Mukaiyama RedOx Hydration
  69. 64 Nazarov Cyclization
  70. 65 Nef Reaction
  71. 66 Negishi Cross-Coupling
  72. 67 Norrish Type I and II Reactions
  73. 68 Olefin (Alkene) Metathesis
  74. 69 Oppenauer Oxidation
  75. 70 Ozonolysis
  76. 71 Paal–Knorr Syntheses
  77. 72 Paternò–Büchi Reaction
  78. 73 Pauson–Khand Reaction
  79. 74 Peptide (Amide) Coupling
  80. 75 Pictet–Spengler Reaction
  81. 76 Pinacol–Pinacolone Rearrangement
  82. 77 Polonovski Reaction
  83. 78 Prilezhaev Epoxidation
  84. 79 Prins Reaction
  85. 80 Pummerer Rearrangement
  86. 81 Ramberg–Bäcklund Rearrangement
  87. 82 Reformatsky Reaction
  88. 83 Robinson Annulation
  89. 84 Shapiro Reaction
  90. 85 Sonogashira Cross-Coupling
  91. 86 Staudinger Reaction
  92. 87 Steglich Esterification
  93. 88 Stille Cross-Coupling
  94. 89 Suzuki Cross-Coupling
  95. 90 Swern Oxidation
  96. 91 Ugi Reaction
  97. 92 Ullmann Aryl–Aryl Coupling
  98. 93 Upjohn Dihydroxylation
  99. 94 Vilsmeier–Haack Reaction
  100. 95 Wacker Oxidation
  101. 96 Wagner–Meerwein Rearrangement
  102. 97 Weinreb Ketone Synthesis
  103. 98 Wittig Reaction
  104. 99 Wohl–Ziegler Reaction
  105. 100 Wolff–Kishner Reduction
  106. Acknowledgments