Organic Chemistry Complete Course

Organic Chemistry Complete Course

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1.1 Lewis Structures | Organic Chemistry Complete Course

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1.1 Lewis Structures | Organic Chemistry Complete Course

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Organic Chemistry Complete Course

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  1. 1 1.1 Lewis Structures | Organic Chemistry Complete Course
  2. 2 1.2 Formal Charges | Organic Chemistry
  3. 3 1.3 Valence Bond Theory and Hybridization | Organic Chemistry
  4. 4 1.4 Molecular Orbital Theory (MO Theory) | Organic Chemistry
  5. 5 1.5 Polarity | Organic Chemistry
  6. 6 1.6 Intermolecular Forces | Organic Chemistry
  7. 7 2.1 Condensed Structures | Organic Chemistry
  8. 8 2.2 Drawing Line Angle Structures (aka Bond Line Structures) | Organic Chemistry
  9. 9 2.3 Identifying Functional Groups | Organic Chemistry
  10. 10 2.4 Resonance | Organic Chemistry
  11. 11 3.1 Introduction to Acids and Bases | Organic Chemistry
  12. 12 3.2 Ranking Acids and Bases | Organic Chemistry
  13. 13 4.1 IUPAC Nomenclature of Alkanes and Cycloalkanes | Organic Chemistry
  14. 14 4.2 Naming Complex Substituents | Organic Chemistry
  15. 15 4.3 IUPAC Nomenclature of Bicyclic Compounds | Organic Chemistry
  16. 16 4.4 Drawing Structural Isomers | Organic Chemistry
  17. 17 4.5 Newman Projections | Organic Chemistry
  18. 18 4.6 Cycloalkanes and Cyclohexane Chair Conformations | Organic Chemistry
  19. 19 5.1 Overview of Isomers | Constitutional Isomers and Stereoisomers | Organic Chemistry
  20. 20 5.2 How to Assign R and S Configuration | Absolute Configuration | Organic Chemistry
  21. 21 5.3 Molecules with Multiple Chiral Centers | Enantiomers, Diastereomers, and Meso Compounds | OChem
  22. 22 5.4 Fischer Projections | Organic Chemistry
  23. 23 5.5 How to Identify Type of Isomerism | Organic Chemistry
  24. 24 5.6 Amine Inversion and Chiral Molecules without Chiral Centers (Allene & Biphenyl) | Organic
  25. 25 5.7 Optical Activity | Organic Chemistry
  26. 26 6.1 Reaction Enthalpy and Bond Dissociation Energy | Organic Chemistry
  27. 27 6.2 Entropy, Gibbs Free Energy, and the Equilibrium Constant | Organic Chemistry
  28. 28 6.3 The Kinetics of Organic Reactions | Organic Chemistry
  29. 29 6.4 Nucleophiles, Electrophiles, and Intermediates | Organic Chemistry
  30. 30 6.5 Curved Arrow Pushing in Reaction Mechanisms | Organic Chemistry
  31. 31 7.1 SN2 Reaction | Organic Chemistry
  32. 32 7.2 SN1 Reactions | Organic Chemistry
  33. 33 7.3 SN1 vs SN2 | Organic Chemistry
  34. 34 7.4 Introduction to Elimination Reactions [Zaitsev's Rule and the Stability of Alkenes] | OChemistry
  35. 35 7.5 E2 Reactions | Organic Chemistry
  36. 36 7.6 E1 Reactions and E1 vs E2 | Organic Chemistry
  37. 37 7.7 How to Distinguish Between Substitution and Elimination Reactions (SN2 SN1 E2 E1) | OChem
  38. 38 8.0 Naming Alkenes IUPAC | Organic Chemistry
  39. 39 8.1 Introduction to Alkene Addition Reactions; Markovnikov's Rule and Syn vs Anti | OChemistry
  40. 40 8.2 Hydrohalogenation of Alkenes | Organic Chemistry
  41. 41 8.3 Acid Catalyzed Hydration, Oxymercuration Demercuration, and Hydroboration Oxidation | OChemistry
  42. 42 8.4 Addition of an Alcohol | Acid-Catalyzed Addition and Alkoxymercuration-Demercuration | OChem
  43. 43 8.5 Catalytic Hydrogenation of Alkenes and Heats of Hydrogenation | Organic Chemistry
  44. 44 8.6 Halogenation of Alkenes and Halohydrin Formation | Organic Chemistry
  45. 45 8.7 Expoxidation, Anti-Dihydroxylation, and Syn-Dihydroxylation of Alkenes | Organic Chemistry
  46. 46 8.8 How to Predict the Products of Alkene Addition Reactions | Organic Chemistry
  47. 47 8.9 Ozonolysis of Alkenes, Oxidation of Alkenes with KMnO4 | Oxidative Cleavage | Organic Chemistry
  48. 48 9.1 Naming Alkynes | Organic Chemistry
  49. 49 9.2 Acidity of Alkynes | Organic Chemistry
  50. 50 9.3 Synthesis of Alkynes | Organic Chemistry
  51. 51 9.4 Reduction of Alkynes | Organic Chemistry
  52. 52 9.5 Hydrohalogenation of Alkynes | Organic Chemistry
  53. 53 9.6 Halogenation of Alkynes | Organic Chemistry
  54. 54 9.7 Hydration of Alkynes | Organic Chemistry
  55. 55 9.8 Ozonolysis of Alkynes | Organic Chemistry
  56. 56 9.9 Alkylation of Acetylide Ions from Terminal Alkynes | Organic Chemistry
  57. 57 10.1 Free Radical Halogenation | Organic Chemistry
  58. 58 10.2 The Free Radical Halogenation Mechanism | Organic Chemistry
  59. 59 10.3 Allylic Bromination and Benzylic Bromination with NBS | Organic Chemistry
  60. 60 10.4 Addition of HBr and Peroxide | Organic Chemistry
  61. 61 11.1 Introduction to Organic Synthesis | Retrosynthesis | Organic Chemistry
  62. 62 11.2 Common Patterns in Organic Synthesis Involving Alkenes | Retrosynthesis | Organic Chemistry
  63. 63 11.3 Common Patterns in Organic Synthesis Involving Alkynes | Organic Chemistry
  64. 64 12.1 Naming Alcohols | Organic Chemistry
  65. 65 12.2 Properties of Alcohols | Organic Chemistry
  66. 66 12.3 Synthesis of Alcohols | Organic Chemistry
  67. 67 12.4 Grignard Reagents | Organic Chemistry
  68. 68 12.5 Protecting Groups for Alcohols | Organic Chemistry
  69. 69 12.6 Substitution Reactions of Alcohols | Organic Chemistry
  70. 70 12.7 Elimination Reactions of Alcohols | Organic Chemistry
  71. 71 12.8 Oxidation of Alcohols by Chromic Acid and PCC | Organic Chemistry
  72. 72 12.9 Organic Synthesis with Alcohols | Organic Chemistry
  73. 73 13.1 Naming Ethers | Organic Chemistry
  74. 74 13.2 Synthesis of Ethers | Organic Chemistry
  75. 75 13.3 Reactions of Ethers | Organic Chemistry
  76. 76 13.4 Naming Epoxides | Organic Chemistry
  77. 77 13.5 Synthesis of Epoxides | Organic Chemistry
  78. 78 13.6 Ring Opening of Epoxides | Organic Chemistry
  79. 79 13.7 Thiols | Organic Chemistry
  80. 80 13.8 Sulfides | Organic Chemistry
  81. 81 13.9 Organic Synthesis with Ethers and Epoxides | Retrosynthesis | Organic Chemistry
  82. 82 14.1 Introduction to IR Spectroscopy | Organic Chemistry
  83. 83 14.2a IR Spectra of Carbonyl Compounds | Organic Chemistry
  84. 84 14.2b The Effect of Conjugation on the Carbonyl Stretching Frequency | Organic Chemistry
  85. 85 14.3 Interpreting More IR Spectra | Organic Chemistry
  86. 86 14.4 Introduction to Mass Spectrometry | Organic Chemistry
  87. 87 14.5 Isotope Effects in Mass Spectrometry | Organic Chemistry
  88. 88 14.6a Fragmentation Patterns of Alkanes, Alkenes, and Aromatic Compounds | Mass Spectrometry
  89. 89 14.6b Fragmentation Patterns of Alkyl Halides, Alcohols, and Amines | Mass Spectrometry
  90. 90 14.6c Fragmentation Patterns of Ketones and Aldehydes | Mass Spectrometry
  91. 91 15.1 Introduction to NMR | Organic Chemistry
  92. 92 15.2 The Number of Signals in C 13 NMR | Organic Chemistry
  93. 93 15.3 The Number of Signals in Proton NMR | Organic Chemistry
  94. 94 15.4 Homotopic vs Enantiotopic vs Diastereotopic | Organic Chemistry
  95. 95 15.5a The Chemical Shift in C 13 and Proton NMR | Organic Chemistry
  96. 96 15.5b The Integration or Area Under a Signal in Proton NMR | Organic Chemistry
  97. 97 15.5c The Splitting or Multiplicity in Proton NMR | Organic Chemistry
  98. 98 15.6a Interpreting NMR Example 1 | Organic Chemistry
  99. 99 15.6b Interpreting NMR Example 2 | Organic Chemistry
  100. 100 15.6c Interpreting NMR Example 3 | Organic Chemistry
  101. 101 15.6d Structural Determination From All Spectra Example 4 | Organic Chemistry
  102. 102 15.6e Structural Determination From All Spectra Example 5 | Organic Chemistry
  103. 103 15.7 Complex Splitting | NMR | Organic Chemistry
  104. 104 16.1 Conjugated Systems and Heats of Hydrogenation | Organic Chemistry
  105. 105 16.2a Pi Molecular Orbitals of 1,3 Butadiene | Organic Chemistry
  106. 106 16.2b Pi Molecular Orbitals of the Allyl System | Organic Chemistry
  107. 107 16.2c Pi Molecular Orbitals of 1,3,5-Hexatriene | Organic Chemistry
  108. 108 16.3 UV/Vis Spectroscopy | Organic Chemistry
  109. 109 16.4 Electrophilic Addition to Conjugated Dienes | Organic Chemistry
  110. 110 16.5 Diels-Alder Reactions | Organic Chemistry
  111. 111 16.6 Cycloaddition Reactions | Organic Chemistry
  112. 112 16.7 Electrocyclic Reactions | Organic Chemistry
  113. 113 16.8 Sigmatropic Rearrangements | Organic Chemistry
  114. 114 17.1 Naming Benzenes | Organic Chemistry
  115. 115 17.2 Aromatic vs Antiaromatic vs Nonaromatic | Organic Chemistry
  116. 116 17.3 The Effects of Aromaticity on Reactivity | Organic Chemistry
  117. 117 17.4 Pi Molecular Orbitals of Benzene | Organic Chemistry
  118. 118 18.1 Electrophilic Aromatic Substitution (EAS Reactions) | Organic Chemistry
  119. 119 18.2 Friedel Crafts Alkylation and Acylation | Organic Chemistry
  120. 120 18.3 Ortho-Para Directors vs Meta Directors in EAS Reactions | Organic Chemistry
  121. 121 18.4 Catalytic Hydrogenation and the Birch Reduction | Organic Chemistry
  122. 122 18.5 Side Chain Reactions of Benzenes | Organic Chemistry
  123. 123 18.6 Nucleophilic Aromatic Substitution (NAS) | Organic Chemistry
  124. 124 18.7 Retrosynthesis with Aromatic Compounds | Organic Chemistry
  125. 125 19.1 Naming Ketones and Aldehydes | Organic Chemistry
  126. 126 19.2 Synthesis of Ketones and Aldehydes | Organic Chemistry
  127. 127 19.3 Introduction to Nucleophilic Addition of Ketones and Aldehydes | Organic Chemistry
  128. 128 19.4a Formation of Hemiacetals and Acetals (Nucleophilic Addition of Alcohols) | Organic Chemistry
  129. 129 19.4b Cyclic Acetals as Protecting Groups for Alcohols | Organic Chemistry
  130. 130 19.5 Imine and Enamine Formation | Addition of Amines | Organic Chemistry
  131. 131 19.6 Reduction of Ketones and Aldehydes (NaBH4 and LiAlH4) | Organic Chemistry
  132. 132 19.7a Addition of Grignard Reagents (and other Carbon Nucleophiles)
  133. 133 19.7b Wittig Reaction | Organic Chemistry
  134. 134 19.8 Baeyer Villiger Oxidation | Organic Chemistry
  135. 135 19.9 Retrosynthesis with Aldehydes and Ketones | Organic Chemistry
  136. 136 20.1 Naming Carboxylic Acids and Carboxylic Acid Derivatives | Organic Chemistry
  137. 137 20.2 Nucleophilic Acyl Substitution | Organic Chemistry
  138. 138 20.3 The Mechanisms of Nucleophilic Acyl Substitution | Organic Chemistry
  139. 139 20.4 Reaction with Grignard Reagents and Gilman Reagents | Carboxylic Acid Derivatives
  140. 140 20.5 Hydride Reduction Reactions | Carboxylic Acid Derivatives | Organic Chemistry
  141. 141 20.6 Synthesis and Reactions of Acid Halides | Organic Chemistry
  142. 142 20.7 Synthesis and Reactions of Acid Anhydrides | Organic Chemistry
  143. 143 20.8 Synthesis and Reactions of Esters | Organic Chemistry
  144. 144 20.9 Properties, Synthesis, and Reactions of Carboxylic Acids | Organic Chemistry
  145. 145 20.10 Synthesis and Reactions of Amides | Organic Chemistry
  146. 146 20.11 Synthesis and Reactions of Nitriles | Organic Chemistry
  147. 147 20.12 Retrosynthesis with Carboxylic Acids Derivatives | Organic Chemistry
  148. 148 21.1 Acidity of the Alpha Hydrogen | Organic Chemistry
  149. 149 21.2 Mechanisms of Alpha Substitution Reactions | Organic Chemistry
  150. 150 21.3 Alpha Halogenation | Organic Chemistry
  151. 151 21.4 Alpha Alkylation | Organic Chemistry
  152. 152 21.5 Aldol Reactions | Organic Chemistry
  153. 153 21.6 Claisen Condensation Reactions | Organic Chemistry
  154. 154 21.7 Malonic Ester Synthesis and Acetoacetic Ester Synthesis | Organic Chemistry
  155. 155 21.8 Michael Reactions | Organic Chemistry
  156. 156 21.9 Robinson Annulation | Organic Chemistry
  157. 157 21.10 Retrosynthesis with Enolates and Enols | Organic Chemistry
  158. 158 22.1 Naming Amines | Organic Chemistry
  159. 159 22.2 Basicity of Amines | Organic Chemistry
  160. 160 22.3 Synthesis of Amines | Organic Chemistry
  161. 161 22.4 Hofmann Elimination and Cope Elimination | Organic Chemistry
  162. 162 22.5 Sandmeyer Reactions | Organic Chemistry
  163. 163 22.6 EAS Reactions with Nitrogen Heterocycles | Organic Chemistry
  164. 164 22.7 Retrosynthesis with Amines | Organic Chemistry
  165. 165 24.1 Classification of Monosaccharides | Organic Chemistry
  166. 166 24.2 Reactions of Monosaccharides | Organic Chemistry
  167. 167 24.3 Disaccharides and Polysaccharides | Organic Chemistry

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