Thư viện Trường Đại học Phú Xuân
Foundations of Organic Chemistry

Nguồn ngoài

Foundations of Organic Chemistry

This resource is aligned with course objectives to master foundations of organic chemistry.

Tác giả
Renee LeClair
Nhà xuất bản
Virginia Tech
Nguồn
LibreTexts
Giấy phép
CC BY-NC-SA
Ngôn ngữ
EN
Danh mục
Khoa học cơ bản
Mục lục· 147 mục
  1. 01: Matter and Solutions
  2. 1.01: What is Chemistry
  3. 1.02: The Classification of Matter
  4. 1.03: Solutions
  5. 1.04: The Dissolution Process
  6. 1.05: Intermolecular Forces
  7. 1.S: Chemistry and Matter (Summary)
  8. 02: Elements Atoms and the Periodic Table
  9. 2.01: The Elements
  10. 2.02: Atomic Theory
  11. 2.03: The Structure of Atoms
  12. 2.04: Nuclei of Atoms
  13. 2.05: Atomic Masses
  14. 2.06: Arrangements of Electrons
  15. 2.07: The Periodic Table
  16. 2.S: Elements Atoms and the Periodic Table (Summary)
  17. 03: Ionic Bonding and Simple Ionic Compounds
  18. 3.01: Two Types of Bonding
  19. 3.02: Ions
  20. 3.03: Formulas for Ionic Compounds
  21. 3.04: Ionic Nomenclature
  22. 3.S: Ionic Bonding and Simple Ionic Compounds (Summary)
  23. 04: Covalent Bonding and Simple Molecular Compounds
  24. 4.01: Covalent Bonds
  25. 4.02: Covalent Compounds- Formulas and Names
  26. 4.03: Multiple Covalent Bonds
  27. 4.04: Polar Covalent Bonds and Electronegativity
  28. 4.05: Characteristics of Molecules
  29. 4.06: Intermolecular Forces
  30. 4.07: Naming Binary Molecular Compounds
  31. 4.S: Covalent Bonding and Simple Molecular Compounds (Summary)
  32. 05: Classification and Balancing of Chemical Reactions
  33. 5.01: Chemical Equations
  34. 5.02: Balancing Chemical Equations
  35. 5.03: Acids Bases and Neutralization Reactions
  36. 5.04: Redox Reactions
  37. 5.05: Recognizing Redox Reactions
  38. 5.06: Net Ionic Equations
  39. 5.07: Le Chatelier's Principle
  40. 5.S: Introduction to Chemical Reactions (Summary)
  41. 06: Organic Chemistry of Hydrocarbons
  42. 6.01: Introduction to Organic Chemistry
  43. 6.02: Condensed Structural and Line-Angle Formulas
  44. 6.03: Structures and Names of Alkanes
  45. 6.04: Branched-Chain Alkanes
  46. 6.05: Cycloalkanes
  47. 6.06: IUPAC Nomenclature
  48. 6.07: Alkenes- Structure and Nomenclature
  49. 6.08: Alkenes- Cis-Tran Isomerization
  50. 6.09: Alkynes
  51. 6.10: Aromatic Compounds
  52. 6.11: Aromatic Compounds- Structure and Nomenclature
  53. 6.12: Physical Properties of Hydrocarbons
  54. 6.13: Chapter Summary
  55. 6.E: Unsaturated and Aromatic Hydrocarbons (Exercises)
  56. 07: Organic Compounds of Oxygen
  57. 7.01: Prelude to Organic Compounds of Oxygen
  58. 7.02: Organic Compounds with Functional Groups
  59. 7.03: Alcohols - Nomenclature and Classification
  60. 7.04: Physical Properties of Alcohols
  61. 7.05: Phenols
  62. 7.06: Ethers
  63. 7.07: Aldehydes and Ketones- Structure and Names
  64. 7.08: Properties of Aldehydes and Ketones
  65. 7.S: Organic Compounds of Oxygen (Summary)
  66. 08: Acids and Bases
  67. 8.01: Brnsted-Lowry Definition of Acids and Bases
  68. 8.02: Water is both an Acid and a Base
  69. 8.03: The Strengths of Acids and Bases
  70. 8.04: pH and Kw
  71. 8.05: Buffers
  72. 8.06: Chapter Summary
  73. 09: Organic Acids and Bases and Some of Their Derivatives
  74. 9.01: Prelude to Organic Acids and Bases and Some of Their Derivatives
  75. 9.02: Carboxylic Acids - Structures and Names
  76. 9.03: The Formation of Carboxylic Acids
  77. 9.04: Physical Properties of Carboxylic Acids
  78. 9.05: Chemical Properties of Carboxylic Acids- Ionization and Neutralization
  79. 9.06: Esters - Structures and Names
  80. 9.07: Physical Properties of Esters
  81. 9.08: Preparation of Esters
  82. 9.09: Hydrolysis of Esters
  83. 9.S: Organic Acids and Bases and Some of Their Derivatives (Summary)
  84. 10: Functional Group Reactions
  85. 10.01: Oxidation-Reduction (Redox) Reactions
  86. 10.02: Redox Reactions in Organic Chemistry
  87. 10.03: Reactions that Form Alcohols
  88. 10.04: Reactions of Alcohols
  89. 10.05: The Formation of Carboxylic Acids
  90. 10.06: Properties of Esters
  91. 10.07: Hydrolysis of Esters
  92. 10.08: Hydrolysis of Amides
  93. 10.09: Summary
  94. 11: Carbohydrates
  95. 11.01: Prelude to Carbohydrates
  96. 11.02: Carbohydrates
  97. 11.03: Classes of Monosaccharides
  98. 11.04: Important Hexoses
  99. 11.05: Cyclic Structures of Monosaccharides
  100. 11.06: Properties of Monosaccharides
  101. 11.07: Disaccharides
  102. 11.08: Polysaccharides
  103. 11.S: Carbohydrates (Summary)
  104. 12: Lipids
  105. 12.01: Prelude to Lipids
  106. 12.02: Fatty Acids
  107. 12.03: Fats and Oils
  108. 12.04: Membranes and Membrane Lipids
  109. 12.05: Steroids
  110. 12.S: Lipids (Summary)
  111. 13: Proteins and Enzymes
  112. 13.01: Properties of Amino Acids
  113. 13.02: Reactions of Amino Acids
  114. 13.03: Organic Sulfur Compounds
  115. 13.04: Amines - Structures and Names
  116. 13.05: Physical Properties of Amines
  117. 13.06: Amines as Bases
  118. 13.07: Amides- Structures and Names
  119. 13.08: Physical Properties of Amides
  120. 13.09: Formation of Amides
  121. 13.10: Chemical Properties of Amides- Hydrolysis
  122. 13.11: Peptides
  123. 13.12: Proteins
  124. 13.13: Enzymes
  125. 13.14: Enzymatic Catalysis
  126. 13.15: Enzyme Activity
  127. 13.16: Enzyme Regulation
  128. 13.17: Enzyme Cofactors and Vitamins
  129. 13.18: Chapter Summary
  130. 14: Nucleic Acids
  131. 14.01: Nucleotides
  132. 14.02: Nucleic Acid Structure
  133. 14.03: Chapter Summary
  134. 15: Flow of Genetic Information
  135. 15.01: Replication and Expression of Genetic Information
  136. 15.02: Translation
  137. 15.03: Mutations and Genetic Diseases
  138. 16: Energy Metabolism
  139. 16.01: Prelude to Energy Metabolism
  140. 16.02: ATP- the Universal Energy Currency
  141. 16.03: Stage I of Catabolism
  142. 16.04: Overview of Stage II of Catabolism
  143. 16.05: Stage III of Catabolism
  144. 16.06: Stage II of Carbohydrate Catabolism
  145. 16.07: Stage II of Lipid Catabolism
  146. 16.08: Stage II of Protein Catabolism
  147. 16.S: Energy Metabolism (Summary)