
- 288 pages
- English
- PDF
- Available on iOS & Android
Name Reactions in Organic Chemistry
About this book
Name Reactions in Organic Chemistry, 2nd Edition, incorporates new, pertinent material and brings up to date the name reactions described in the first edition. Along with this revision, several additional name reactions have been included. As with the first edition, the selections were based on general interest, recurrence in the literature, and the contributions of the ""name chemist"" to the historical development of organic chemistry. Although the writer does not pretend to be an historian of chemistry, it seemed desirable to include, along with the reactions, pertinent information regarding the chemist's background, his training, his contemporaries, and his contributions. This book contains 103 name reactions, arranged alphabetically. The general plan was to present a description of each reaction, its scope, applicability, and limitations, and to bring it up to date in regard to any new developments.
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Information
Table of contents
- Front Cover
- Name Reactions in Organic Chemistry
- Copyright Page
- Table of Contents
- Preface to Second Edition
- Preface to First Edition
- Chapter 1. Arndt-Eistert Synthesis
- Chapter 2. Baeyer-Villiger Oxidation
- Chapter 3. Barbier-Wieland Degradation
- Chapter 4. Bart Reaction
- Chapter 5. Bechamp Reduction
- Chapter 6. Beckmann Rearrangement
- Chapter 7. Birch Reduction
- Chapter 8. Bischler-Napieralski Reaction
- Chapter 9. Blanc Chloromethylation Reaction
- Chapter 10. Bouveault-Blanc1 Reduction
- Chapter 11. Bouveault Aldehyde Synthesis
- Chapter 12. Von Braun Reaction
- Chapter 13. Von Braun Degradation
- Chapter 14. Bucherer Reaction
- Chapter 15. Bucherer Hydantoin Synthesis
- Chapter 16. Camps Reaction
- Chapter 17. Cannizzaro Reaction
- Chapter 18. Chugaev Reaction
- Chapter 19. Claisen Condensation
- Chapter 20. Claisen Rearrangement
- Chapter 21. Claisen-Schmidt Condensation
- Chapter 22. Clemmensen Reduction
- Chapter 23. Combes Quinoline Synthesis
- Chapter 24. Conrad-Limpach Synthesis
- Chapter 25. Curtius Reaction
- Chapter 26. Dakin Reaction
- Chapter 27. Dakin-West Reaction
- Chapter 28. Darzens Glycidic Ester Condensation
- Chapter 29. Darzens Synthesis of Unsaturated Ketones
- Chapter 30. Delepine Reaction
- Chapter 31. Dieckmcmn Reaction
- Chapter 32. Diels-Alder Reaction
- Chapter 33. Doebner Synthesis
- Chapter 34. Doebner-Miller Synthesis
- Chapter 35. Duff Reaction
- Chapter 36. Elbs Reaction
- Chapter 37. Elbs Persulfate Oxidation
- Chapter 38. Emde Degradation
- Chapter 39. Erlenmeyer-Plochl Azlactone Synthesis
- Chapter 40. Faworskii Rearrangement
- Chapter 41. Fischer Indole Synthesis
- Chapter 42. Friedel-Crafts Reaction
- Chapter 43. Friedldnder Synthesis
- Chapter 44. Fries Reaction
- Chapter 45. Gabriel Synthesis
- Chapter 46. Gattermann Aldehyde Synthesis
- Chapter 47. Gattermann Reaction
- Chapter 48. Gattermann-Koch Reaction
- Chapter 49. Gomberg-Bachmann-Hey Reaction
- Chapter 50. Gould-Jacobs Reaction
- Chapter 51. Graebe-Ullmann Synthesis
- Chapter 52. Grignard Reaction
- Chapter 53. Hantzsch Pyridine Synthesis
- Chapter 54. Hell-Volhard-Zelinsky Reaction
- Chapter 55. Hoesch Synthesis
- Chapter 56. Hofmann Reaction
- Chapter 57. Hofmann Degradation
- Chapter 58. Hunsdiecker Reaction
- Chapter 59. Ivanov Reaction
- Chapter 60. Jacobsen Reaction
- Chapter 61. Knoevenagel Reaction
- Chapter 62. Knorr Pyrrole Synthesis -
- Chapter 63. Kolbe-Schmitt Reaction
- Chapter 64. Kolbe's Electrochemical Reaction
- Chapter 65. Leuckart Reaction
- Chapter 66. Lossen Rearrangement
- Chapter 67. McFadyen-Stevens Reduction
- Chapter 68. Mannich Reaction
- Chapter 69. Meerwein Condensation
- Chapter 70. Meerwein-Ponndorf-Verley Reduction
- Chapter 71. Michael Reaction
- Chapter 72. Nef Reaction
- Chapter 73. Oppenauer Oxidation
- Chapter 74. Passerini Reaction
- Chapter 75. Pechmann Condensation
- Chapter 76. Perkin Reaction
- Chapter 77. Pfitzinger Reaction
- Chapter 78. Pictet-Spengler Reaction
- Chapter 79. Pomeranz-Fritsch Reaction
- Chapter 80. Prins Reaction
- Chapter 81. Pschorr Synthesis
- Chapter 82. Reformatsky Reaction
- Chapter 83. Reimer-Tiemann Reaction
- Chapter 84. Reissert Reaction
- Chapter 85. Rosenmund Reduction
- Chapter 86. Sandmeyer Reaction
- Chapter 87. Schiemann Reaction
- Chapter 88. Schmidt Reaction
- Chapter 89. Skraup Reaction
- Chapter 90. Sommelet Reaction
- Chapter 91. Stephen Reaction
- Chapter 92. Stevens Rearrangement
- Chapter 93. Stobbe Condensation
- Chapter 94. Stork Reaction
- Chapter 95. Ullmann Reaction
- Chapter 96. Ullmann Condensation
- Chapter 97. Wallach Reaction
- Chapter 98. Willgerodt Reaction
- Chapter 99. Williamson Synthesis
- Chapter 100. Wittig Reaction
- Chapter 101. Wohl-Ziegler Reaction
- Chapter 102. Wolff-Kishner Reduction
- Chapter 103. Wurtz Reaction
- Subject Index