List of Name reactions

Following is the lists of organic name reactions:

1. Acetoacetic Ester Synthesis
2. Acyloin Condensation
3. Aldol Addition + Aldol Condensation
4. Appel Reaction
5. Arbuzov Reaction = Michaelis-Arbuzov Reaction
6. Arndt-Eistert Synthesis
7. Azo Coupling
8. Baeyer-Villiger Oxidation
9. Balz-Schiemann Reaction = Schiemann Reaction
10. Bamford-Stevens Reaction
11. Barton Decarboxylation
12. Barton-McCombie Reaction (Barton Desoxygenation)
13. Baylis-Hillman Reaction
14. Beckmann Rearrangement
15. Benzilic Acid Rearrangement
16. Benzoin Condensation
17. Bergman Cyclization
18. Birch Reduction
19. Bouveault-Blanc Reduction
20. Buchwald-Hartwig Cross Coupling Reaction
21. Cadiot-Chodkiewicz Coupling
22. Cannizzaro Reaction
23. Chugaev Reaction
24. Claisen Condensation
25. Claisen Rearrangement
26. Clemmensen Reduction
27. Cope Elimination
28. Cope Rearrangement
29. Corey-Seebach Reaction
30. Criegee Reaction
31. Curtius Rearrangement
32. Delépine Reaction
33. De Mayo Reaction
34. Dess-Martin Oxidation
35. Diazotisation and Azo Coupling
36. Dieckmann Condensation
37. Diels-Alder Reaction
38. Di-π-Methane Rearrangement
39. Dötz Reaction
40. Eglinton Reaction
41. Ene Reaction = Alder-Ene Reaction
42. Jacobsen Epoxidation
43. Ester Pyrolysis
44. Favorskii Reaction
45. Finkelstein Reaction
46. Friedel-Crafts Acylation
47. Friedel-Crafts Alkylation
48. Gabriel Synthesis
49. Gattermann-Koch Reaction
50. Glaser Coupling and Hay Coupling
51. Grignard Reaction
52. Grob Fragmentation
53. Grubbs Olefin Metathesis
54. Haloform Reaction
55. Heck Reaction
56. Hell-Volhard-Zelinsky Reaction
57. Henry Reaktion
58. Hofmann Elimination
59. Hofmann's Rule
60. Horner-Wadsworth-Emmons Reaction
61. Hunsdiecker Reaction
62. Hydroboration
63. Ireland-Claisen Rearrangement
64. Knoevenagel Condensation
65. Kolbe Reaction
66. Kolbe-Schmitt Reaction
67. Kumada–Negishi Coupling
68. Leuckart–Wallach (Leuckart) Reaction
69. Malonic Ester Synthesis
70. Mannich Reaction
71. Markovnikov's Rule
72. McMurry Reaction
73. Meerwein-Ponndorf-Verley Reduction
74. Michael Addition
75. Mitsunobu Reaction
76. Mukaiyama Aldol Addition
77. Negishi Coupling
78. Norrish-Type I and II
79. Nozaki-Hiyama Coupling
80. Nucleophilic Substitution (SN1 / SN2)
81. Oppenauer Oxidation
82. Oxy-Cope Rearrangement
83. Paterno-Büchi Reaction
84. Pauson-Khand Reaction
85. Perkin Reaction
86. Peterson Olefination
87. Pinacol Coupling Reaction
88. Pinacol Rearrangement
89. Prilezhaev Epoxidation
90. Reformatsky Reaction
91. Ritter Reaction
92. Robinson Annulation
93. Rosenmund Reduction
94. Sakurai Reaction (Hosomi Sakurai)
95. Sandmeyer Reaction
96. Sanger’s Reagent
97. Saytzeff's Rule
98. Schiemann Reaction
99. Schmidt Reaction
100. Schotten-Baumann Reaction
101. Sharpless Epoxidation and Dihydroxylation
102. Simmons-Smith Reaction
103. Sonogashira Coupling
104. Staudinger Reaction
105. Stille Coupling
106. Strecker Synthesis
107. Suzuki Coupling
108. Swern Oxidation
109. Tebbe Olefination
110. Thorpe Reaction
111. Tishhenko Reaction
112. Ullmann Reaction
113. Vilsmeier Reaction
114. Wacker-Tsuji Oxidation
115. Willgerodt-Kindler Reaction
116. Williamson Synthesis
117. Wittig Olefination
118. Wittig Rearrangement
119. Wittig-Horner Reaction
120. Wohl-Ziegler Reaction
121. Wolff Rearrangement
122. Wolff-Kishner Reduction
123. Wurtz Reaction
124. Wurtz-Fittig Reaction

We will go through these reactions one by one.

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