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Organic Reactions: Mechanism with Problems / Tyagi, Rajpal
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Organic Reactions: Mechanism with Problems
Tyagi, Rajpal
 
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  Book ID : 28895
  ISBN-10 : 81-8356-012-1 / 8183560121
  ISBN-13 : 978-81-8356-012-2 / 9788183560122
  Place of Publication : Delhi
  Year of Publication : 2015
  Edition : (Reprint)
  Language : English
  xi, 498p., 23 cm. (First Edition pub. in 2005)
   
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 CONTENTS
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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.

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 DESCRIPTION
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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 is 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.
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