Thư viện Trường Đại học Phú Xuân
Organic Chemistry II

Nguồn ngoài

Organic Chemistry II

Welcome to organic chemistry! This text has been written for students. It emphasizes the practical details and skills needed to master this challenging subject. Learning organic chemistry is brain yoga! Our brains become strong and flexible with practice. This textmap is for Semester II and can be printed at the online LibreTexts Bookstore.

Tác giả
Wade Textmap
Nhà xuất bản
LibreTexts
Nguồn
LibreTexts
Ngôn ngữ
EN
Danh mục
Khoa học cơ bản
Mục lục· 199 mục
  1. 13: Structure and Synthesis of Alcohols
  2. 13.01: Introduction to Structure and Synthesis of Alcohols
  3. 13.02: Classification of Alcohols
  4. 13.03: Physical Properties of Alcohols
  5. 13.04: Spectroscopy of Alcohols
  6. 13.05: Acidity of Alcohols and Phenols
  7. 13.06: Synthesis of Alcohols - Review
  8. 13.07: Reduction of the Carbonyl Group - Synthesis of 1 and 2 Alcohols
  9. 13.08: Organometallic Reagents
  10. 13.09: Organometallic Reagents in Alcohol Synthesis
  11. 13.10: Thiols (Mercaptans)
  12. 13.11: Commercially Important Alcohols
  13. 13.12: 13.12 Additional Exercises
  14. 13.13: Solutions to Additional Exercises
  15. 14: Reactions of Alcohols
  16. 14.01: Reactions of Alcohols with Hydrohalic Acids
  17. 14.02: Reactions with Phosphorus Halides and Thionyl Chloride
  18. 14.03: Alcohol conversion to Esters - Tosylate and Carboxylate
  19. 14.04: Dehydration Reactions of Alcohols
  20. 14.05: Oxidation States of Alcohols and Related Functional Groups
  21. 14.06: Oxidation Reactions of Alcohols
  22. 14.07: Determining Alcohol Classifications in the Lab - alternate reactions
  23. 14.08: Protection of Alcohols
  24. 14.09: Cleavage of Diols
  25. 14.10: Reactions of Alkoxides
  26. 14.11: Biological Oxidation - An Introduction
  27. 14.12: Additional Exercises
  28. 14.13: Solutions to Additional Exercises
  29. 15: Ethers Epoxides and Thioethers
  30. 15.01: Physical Properties of Ethers
  31. 15.02: Spectroscopy of Ethers
  32. 15.03: The Williamson Ether Synthesis
  33. 15.04: Alkoxymercuration-Demercuration Synthesis of Ethers
  34. 15.05: Acidic Cleavage of Ethers
  35. 15.06: Autoxidation of Ethers
  36. 15.07: Synthesis of Epoxides
  37. 15.08: Opening of Epoxides
  38. 15.09: Reactions of Epoxides with Grignard and Organolithium Reagents
  39. 15.10: Crown Ethers
  40. 15.11: Epoxy Resins - The Advent of Modern Glues
  41. 15.12: Thioethers (Sulfides) and Silyl Ethers
  42. 15.13: Additional Exercises
  43. 15.14: Solutions to Additional Exercises
  44. 16: Conjugated Systems Orbital Symmetry and Ultraviolet Spectroscopy
  45. 16.01: Stability of Conjugated Dienes - Molecular Orbital Theory
  46. 16.02: Allylic Cations
  47. 16.03: Electrophilic Additions to Conjugated Dienes
  48. 16.04: Kinetic versus Thermodynamic Control
  49. 16.05: SN2 Reactions of Allylic Halides and Tosylates
  50. 16.06: The Diels-Alder (4 2) Cycloaddition Reaction
  51. 16.07: Diels-Alder Stereochemistry
  52. 16.08: Diene Polymers - Natural and Synthetic Rubbers
  53. 16.09: Structure Determination in Conjugated Systems - Ultraviolet Spectroscopy
  54. 16.10: Interpreting Ultraviolet Spectra - The Effect of Conjugation
  55. 16.11: Conjugation Color and the Chemistry of Vision
  56. 16.12: Additional Exercises
  57. 16.13: Solutions to Additional Exercises
  58. 17: Aromatic Compounds
  59. 17.01: Introduction- The Discovery of Benzene
  60. 17.02: The Structure and Properties of Benzene and its Derivatives
  61. 17.03: Resonance and the Molecular Orbitals of Benzene
  62. 17.04: The Molecular Orbital Picture of Cyclobutadiene
  63. 17.05: Aromaticity and Huckel's Rule
  64. 17.06: Aromatic Ions - a closer look
  65. 17.07: Heterocyclic Aromatic Compounds - a closer look
  66. 17.08: Polycyclic Aromatic Hydrocarbons
  67. 17.09: Spectroscopy of Aromatic Compounds
  68. 17.10: Additional Exercises
  69. 17.11: Solutions to Additional Exercises
  70. 18: Reactions of Aromatic Compounds
  71. 18.01: Electrophilic Aromatic Substitution (EAS)
  72. 18.02: Halogenation of Benzene (an EAS Reaction)
  73. 18.03: Nitration of Benzene (an EAS Reaction)
  74. 18.04: Sulfonation of Benzene (an EAS Reaction)
  75. 18.05: Alkylation and Acylation of Benzene - The Friedel-Crafts EAS Reactions
  76. 18.06: Substituent Effects on the EAS Reaction
  77. 18.07: Side-Chain Reactions of Benzene Derivatives
  78. 18.08: Synthetic Strategies for Di-substituted Benzenes
  79. 18.09: Trisubstituted Benzenes - Effects of Multiple Substituents
  80. 18.10: Nucleophilic Aromatic Substitution - The Addition-Elimantion Mechanism
  81. 18.11: NAS Reactions - the Elimination-Addition (Benzyne) Mechanism
  82. 18.12: Reduction of Aromatic Compounds
  83. 18.13: Additional Exercises
  84. 18.14: Solutions to Additional Exercises
  85. 19: Ketones and Aldehydes
  86. 19.01: Carbonyl Compound Structure and Properties
  87. 19.02: Spectroscopy of Ketones and Aldehydes
  88. 19.03: Review of Ketone and Aldehyde Synthesis
  89. 19.04: 19.4 New Synthesis of Aldehydes and Ketones
  90. 19.05: Nucleophilic Addition Reactions of Ketones and Aldehydes
  91. 19.06: Nucleophilic Addition of Water (Hydration)
  92. 19.07: Nucleophilic Addition of Cyanide and Acetylide
  93. 19.08: Nucleophilic Addition of Grignards
  94. 19.09: Nucelophilic Addition of Amines (Imine and Enamine Formation)
  95. 19.10: Nucleophilic Addition of Hydrazine (Wolff-Kishner Reaction)
  96. 19.11: Nucelophilic Addition of Alcohols (Acetal Formation)
  97. 19.12: Acetals as Protecting Groups
  98. 19.13: Nucelophilic Addition of Phosphorus Ylides (The Wittig Reaction)
  99. 19.14: Oxidation of Aldehydes
  100. 19.15: Reductions of Ketones and Aldehydes
  101. 19.16: Additional Exercises
  102. 19.17: Solutions to Additional Exercises
  103. 20: Amines
  104. 20.01: Structure and Physical Properties of Amines
  105. 20.02: Basicity of Amines and Ammonium Salt Formation
  106. 20.03: Spectroscopy of Amines
  107. 20.04: Synthesis of Amines
  108. 20.05: Synthesis of Primary Amines
  109. 20.06: Reactions of Amines
  110. 20.07: Reactions of Arylamines
  111. 20.08: The Hofmann Elimination- Amines as Leaving Groups
  112. 20.09: Oxidation of Amines - The Cope Elimination
  113. 20.10: Sulfa Drugs - a closer look
  114. 20.11: Additional Exercises
  115. 20.12: Solutions to Additional Exercises
  116. 21: Carboxylic Acids
  117. 21.01: Structure and Properties of Carboxylic Acids and their Salts
  118. 21.02: Acidity of Carboxylic Acids
  119. 21.03: Spectroscopy of Carboxylic Acids
  120. 21.04: Synthesis of Carboxylic Acids
  121. 21.05: Reactions of Carboxylic Acids Overview
  122. 21.06: Condensation of Acids with Alcohols- The Fischer Esterification
  123. 21.07: Methyl Ester Synthesis Using Diazomethane
  124. 21.08: Condensation of Acids with Amines
  125. 21.09: Reduction of Carboxylic Acids
  126. 21.10: Biochemically Interesting Carboxylic Acids
  127. 21.11: Additional Exercises
  128. 21.12: Solutions to Additional Exercises
  129. 22: Carboxylic Acid Derivatives and Nitriles
  130. 22.01: Structure and Physical Properties of Acid Derivatives
  131. 22.02: Spectroscopy of Carboxylic Acid Derivatives
  132. 22.03: Interconversion of Acid Derivatives by Nucleophilic Acyl Substitution
  133. 22.04: Acid Halide Chemistry
  134. 22.05: Acid Anhydride Chemistry
  135. 22.06: Ester Chemistry
  136. 22.07: Amide Chemistry
  137. 22.08: Nitrile Chemistry
  138. 22.09: Thioesters- Biological Carboxylic Acid Derivatives
  139. 22.10: Polyamides and Polyesters- Step-Growth Polymers
  140. 22.11: Beta-Lactams- An Application
  141. 22.12: Biological Acylation Reactions
  142. 22.13: Additional Exercises
  143. 22.14: Solutions to Additional Exercises
  144. 23: Alpha Substitutions and Condensations of Carbonyl Compounds
  145. 23.01: Relative Acidity of alpha-Hydrogens
  146. 23.02: Enols Enolate Ions and Tautomerization
  147. 23.03: Reaction Overview
  148. 23.04: Alpha Halogenation of Carbonyls
  149. 23.05: Bromination of Acids- The HVZ Reaction
  150. 23.06: Alkylation of the alpha-Carbon via the LDA pathway
  151. 23.07: Alkylation of the Alpha-Carbon via the Enamine Pathway
  152. 23.08: The Aldol Reaction and Condensation of Ketones and Aldehydes
  153. 23.09: The Claisen Condensation Reactions of Esters
  154. 23.10: Conjugate Additions- The Michael Reaction
  155. 23.11: Decarboxylation Reactions
  156. 23.12: Additional Exercises
  157. 23.13: Solutions to Additional Exercises
  158. 24: Carbohydrates
  159. 24.01: Introduction
  160. 24.02: Classification of Carbohydrates
  161. 24.03: Fischer Projections
  162. 24.04: D and L Sugars
  163. 24.05: Configuration of Aldoses
  164. 24.06: Cyclic Structures of Monosaccharides
  165. 24.07: Reactions of Monosaccharides
  166. 24.08: Disaccharides and Glycosidic Bonds
  167. 24.09: Polysaccharides
  168. 24.10: Other Important Carbohydrates
  169. 24.11: Cell Surface Carbohydrates and Influenza Viruses
  170. 25: Amino Acids Peptides and Proteins
  171. 25.01: Introduction
  172. 25.02: Structure and Stereochemistry of the Amino Acids
  173. 25.03: Isoelectric Points and Electrophoresis
  174. 25.04: Synthesis of Amino Acids
  175. 25.05: Peptides and Proteins
  176. 25.06: Amino Acid Analysis of Peptides
  177. 25.07: Peptide Sequencing- The Edman Degradation
  178. 25.08: Peptide Synthesis
  179. 25.09: Automated Peptide Synthesis- The Merrifield Solid-Phase Technique
  180. 25.10: Levels of Protein Structure
  181. 25.11: Enzymes and Coenzymes
  182. 25.12: How do enzymes work
  183. 26: Lipids
  184. 26.01: Introduction
  185. 26.02: Waxes Fats and Oils
  186. 26.03: Saponification of Fats and Oils Soaps and Detergents
  187. 26.04: Phospholipids
  188. 26.05: Prostaglandins and other Eicosanoids
  189. 26.06: Terpenes and Terpenoids
  190. 26.07: Steroids
  191. 26.08: Biosynthesis of Steroids
  192. 27: Nucleic Acids
  193. 27.01: Nucleotides and Nucleic Acids
  194. 27.02: DNA Base Pairs
  195. 27.03: DNA Replication
  196. 27.04: Transcription of DNA
  197. 27.05: Translation of RNA- Protein Biosynthesis
  198. 27.06: DNA Sequencing
  199. 27.07: Polymerase Chain Reactions