Organic Reactions : Mechanism with Problems by Rajpal Tyagi

New Delhi: Discovery. Hardbound. As New. Contents Preface. 1. Acyloin reaction or acyloin condensation. 2. Aldol condensation. 3. Allylic rearrangement. 4. Arndt Eister reaction. 5. Beckmann rearrangement. 6. Benzidine rearrangement. 7. Benzoin condensation. 8. Benzilic acid rearrangement. 9. Bischler Napieralski synthesis. 10. Bayer Villiger oxidation. 11. Birch reduction. 12. Blaise reaction. 13. Bouvealt 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 Claissen Schmidt condensation. 23. Cumene hydroperoxide rearrangement. 24. Curtius rearrangement. 25. Cope reaction or 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. Die's alder reaction. 36. Elbs 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 Gatterman koch formylation. 50. Gabriel phthalimide synthesis. 51. Haloform reaction. 52. Haller Bauer reaction. 53. Hydroboration. 54. Harries ozonolysis reaction. 55. Hell volhard zelinsky reaction. 56. Hydrocarboxylation reaction (Koch haaf 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. 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 reaction. 96. Skraup's synthesis. 97. Sonn Muller 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 reactions. 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. The present title Organic Reaction has been designed for under graduate and post graduate student of all Indian universities. We live and breed in a world that owes to organic chemistry many times more than organic chemistry owes to it. The domain of organic chemistry is so enormous that it defies the imagination of any individual let alone mastering it in entirety. This is not a text book but a reference book supplement to the text of organic chemistry meant for university students. However some advanced students may find the book inadequate. It has been constant endeavour of the authors to furnish maximum substance keeping in view the limitations of size of the volume. Efforts have been made to condense the matter as far as practicable. It is hoped that this book will not only meet the requirement of Indian students but will also be useful as a guideline to the teachers in their teaching.