Welcome to www.saujanyabooks.com

CONTENTS:-
1. Acyloin Reaction or acyloin condensation.
2. Aldol condensation.
3. Allylic rearrangement.
4. Arndt-eister reaction.
5. Beckmann rearrangement.
6. Benzidine rearrangement.
7. Bensoin condensation.
8. Benzilic acid rearrangement.
9. Bishchler-napieralski synthesis.
10. Bayer-villiger oxidation.
11. Birch reductin.
12. Blaise reaction.
13. Bouvealth-blance reaction.
14. Bradsher reaction.
15. Cannizzaro reaction.
16. Carbylamine reaction.
17. Chichibabin reaction.
18. Chloromethylation [or blance reaction].
19. Clemmensen reduction.
20. Claisen condensation.
21. Claisen rearrangement.
22. Claissen-schmidt reaction or claisse-schmidt condensation.
23. Cumene hydroperoxide rearrangement.
24. Curtius rearrangement.
25. Cope reaction of cope elimination.
26. Corey-house synthesis.
27. Criegee reaction.
28. Darzens reaction.
29. Dakin reaction.
30. Dakin-west reaction.
31. Duff reaction.
32. Dienone-phenol Rearrangement.
33. Diazotisation [Or griess reaction].
34. Dieckmann condensation.
35. Diel's-Alder reaction.
36. Eibs persulphate Oxidation.
37. Elbs reaction.
38. Ene reaction.
39. Eschweiler-clark reaction.
40. Etard oxidation.
41. Favorskii rearrangement.
42. Fischer-Indole synthesis.
43. Finkelstein reaction.
44. Friedal-craft Alkylation.
45. Fries reannangement.
46. Gattermann reaction.
47. Gattermann-aldehyde synthesis.
48. Gattermann-Amide synthesis.
49. Gattermann-kochaldehyde synthesis or gattermankoch formylation.
50. Gabriel phthalimide synthesis.
51. Haloform reaction.
52. Haller-Bauer reaction.
53. Hydroboration.
54. Harries Ozonolysis reaction.
55. Hell-volhard-zelinsky reaction.
56. Hydrocarbodylation reaction [Koch-haff reaction].
57. Houben-Hoesch reaction.
58. Hofmann rearrangement.
59. Hofmann martius rearrangement.
60. Hunsdiecker reaction.
61. Knoevenagel reaction.
62. Kolbe reaction.
63. Kolbe hydrocarbon synthesis.
64. Kolbe reaction [Electrolytic method].
65. Knorr-paal synthesis.
66. Kolbe-schmidt reaction.
67. Lederer-Manasse reaction.
68. Leuckart reaction.
69. Lossen rearrangement Michael reaction.
70. Michael reaction.
71. Mannich reaction.
72. Meerwein-ponndorf-verley reduction [MPV reduction].
73. Meerwein acylaion reaction.
74. Oppenauer oxidation.
75. Perkin reaction.
76. Perkin markkonikov Krestovnikov-freund synthesis.
77. Pechmann reaction.
78. Pinacol-Pinalcolone rearrangement [Pinacol Rearrangement].
79. Pinner synthesis.
80. Prevost reaction.
81. Prilezhaev reaction.
82. Prins reaction.
83. Ritter reaction.
84. Reimer-tiemann reaction.
85. Reformatsky reaction.
86. Rosenmund's reduction.
87. Rosenmund-von braun reaction.
88. Ruzicka reaction.
89. Robinson Annelation reaction.
90. Sandmeyer reaction.
91. Scholl reaction.
92. Schotten-Baumann reaction.
93. Sandmeyer reaction.
94. Schmidt reaction.
95. Schiemann reactions.
96. Skraup's synthesis.
97. Sonnmuller aldehyde synthesis.
98. Staudinger reaction.
99. Sommelet reaction.
100. simmons-smith reaction.
101. Stobbe condensation.
102. Stephen aldehyde synthesis.
103. Stork Enamine reaction.
104. Strecker Amino acid synthesis.
105. Swern oxidation.
106. Thorpe reaction.
107. Thorpe-ziegler cyclisation.
108. Tollens reaction.
109. Tischenko reaction or tischenko-claisen reaction.
110. Ullmann reaction.
111. Vilsmeier reaction or vilsmeier-haack.
112. Von braun reaction.
113. Wakcer process.
114. Wagner-Meerwein rearrangements.
115. Williamson ether synthesis.
116. Wittig reaction.
117. Wolff-Kishner reduction.
118. Wurtz reaction.
119. Wurtz fittig reaction.