Organic Chemistry: 100 Must-Know Mechanisms
eBook - PDF

Organic Chemistry: 100 Must-Know Mechanisms

  1. 249 pages
  2. English
  3. PDF
  4. Available on iOS & Android
eBook - PDF

Organic Chemistry: 100 Must-Know Mechanisms

About this book

This book summarizes 100 essential mechanisms in organic chemistry ranging from classical such as the Reformatsky Reaction from 1887 to recently elucidated mechanism such as the copper(I)-catalyzed alkyne-azide cycloaddition. The reactions are easy to grasp, well-illustrated and underpinned with explanations and additional information.

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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 & Chemistry. We have over one million books available in our catalogue for you to explore.

Information

Publisher
De Gruyter
Year
2020
Print ISBN
9783110608304
eBook ISBN
9783110608373
Edition
1
Topic
Physical Sciences
Subtopic
Chemistry
Index
Chemistry
https://doi.org/10.1515/9783110608373-001
1 
Electrophilic 
Addition 
Mechanism
Fig. 
1.1:
 Bimolecular 
electrophilic 
addition 
mechanism 
(
Ad
E
2
).
1
1
Symbol 
Ad
E
2
stands 
for 
Ad
dition 
E
lectrophilic 
Bi
-molecular 
(
2
), 
that 
is, 
the 
rate 
of 
the 
reaction 
is 
second 
order
and 
the 
rate-determining 
step 
(i.e., 
the 
slow
step) 
depends 
on 
the 
concentration 
of 
two 

Table of contents

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