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Structure & Reactivity I: Chemical Structure and Properties

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Structure & Reactivity I: Chemical Structure and Properties

Atoms, Compounds, Molecules, Intermolecular Attractions, Structure-Property Relationships

Tác giả
Chris Schaller
Nhà xuất bản
College of Saint Benedict/Saint John's University
Nguồn
LibreTexts
Giấy phép
CC BY-NC
Ngôn ngữ
EN
Danh mục
Khoa học cơ bản
Mục lục· 172 mục
  1. 01: Introduction to Atoms
  2. 1.01: From Democritus to the 19th Century- Historical Developments in Chemistry
  3. 1.02: Old Quantum Mechanics- Basic Developments
  4. 1.03: New Quantum Mechanics
  5. 1.04: Quantum Numbers
  6. 1.05: The Aufbau Process
  7. 1.06: The Periodic Table and Periodic Trends
  8. 1.07: Atoms- Solutions to Selected Problems
  9. 02: Metals
  10. 2.01: Introduction to Metals
  11. 2.02: A Layer of Metal Atoms
  12. 2.03: Building Metal Atoms in Three Dimensions
  13. 2.04: Application Problems with Metals
  14. 2.05: Metals- Solutions to Selected Problems
  15. 03: Ionic Compounds
  16. 3.01: Ionic Atoms
  17. 3.02: Counterions
  18. 3.03: Physical Properties
  19. 3.04: Solubility
  20. 3.05: Structures of Ionic Solids
  21. 3.06: Application Problems
  22. 3.07: Naming Ionic Compounds
  23. 3.08: Ionic Compounds- Solutions for Selected Problems
  24. 04: Introduction to Molecules
  25. 4.01: Why do Molecules Matter
  26. 4.02: Lewis Structures
  27. 4.03: Lewis Structures and Multiple Bonding
  28. 4.04: Lewis Structures and Polyatomic Molecules
  29. 4.05: Lewis and Formal Charge
  30. 4.06: The Need for Resonance Structures
  31. 4.07: Which Bonds are Ionic and Which are Covalent
  32. 4.08: Line Drawings
  33. 4.09: Three Dimensional Drawings
  34. 4.10: Other Geometries
  35. 4.11: Controversial Lewis Structures
  36. 4.12: Organic Functional Groups
  37. 4.13: Common Biomolecules
  38. 4.14: Drawings for Large Biological Compounds
  39. 4.15: Application Problems
  40. 4.16: Solutions to Selected Problems
  41. 05: Stereochemistry
  42. 5.01: Introduction
  43. 5.02: Stereoisomers
  44. 5.03: Stereochemistry - Extra Problems.
  45. 5.04: Enantiomers
  46. 5.05: Simple Organic Enantiomers- R and S configurations
  47. 5.06: Biological Small Molecules
  48. 5.07: Optical Rotation
  49. 5.08: The Polarimetry Experiment
  50. 5.09: Carbohydrates and Diastereomers
  51. 5.10: Diastereomers and Physical Properties
  52. 5.11: Carbohydrates in Cyclic Form
  53. 5.12: Biological Building Blocks- Amino Acids
  54. 5.13: Macromolecular Structures- Alpha-Helices
  55. 5.14: Optical Resolution
  56. 5.15: Another Kind of Stereochemistry- Alkene Isomers
  57. 5.16: E and Z Alkene Isomers
  58. 5.17: Stereoisomers in Other Geometries- Octahedra
  59. 5.18: Enantiomers in Octahedral Complexes
  60. 5.19: Chiral Catalysts for Production of Enantiomerically Pure Compounds
  61. 5.20: Solutions to Selected Problems
  62. 5.21: Biological Building Blocks- Carbohydrates
  63. 06: Conformational Analysis
  64. 6.01: Introduction to Conformation
  65. 6.02: Simple Molecules
  66. 6.03: Conformation of Butane
  67. 6.04: The Basis Set
  68. 6.05: Molecular Modeling
  69. 6.06: Cyclic System
  70. 6.07: Cyclohexane
  71. 6.08: Diamond Lattice Drawings
  72. 6.09: Substituted Cyclohexanes
  73. 6.10: Disubstituted Cyclohexanes
  74. 6.11: Other Rings
  75. 6.12: Rings with Heteroatoms
  76. 6.13: More Practice with Conformation
  77. 6.14: Application Problems
  78. 6.15: Solutions to Selected Problems
  79. 07: Structure-Property Relationships
  80. 7.01: The Properties of Water
  81. 7.02: Changes of State
  82. 7.03: Kinetic-molecular Theory
  83. 7.04: London Interactions
  84. 7.05: Dipole Interactions
  85. 7.06: Hydrogen Bonding
  86. 7.07: Ionic Attractions
  87. 7.08: Comparing Properties of Isomers
  88. 7.09: Miscibility
  89. 7.10: Solubility
  90. 7.11: Hydrogen Bond Acceptors
  91. 7.12: Heterogenous Mixtures
  92. 7.13: Intermolecular Attractions and Protein Structure
  93. 7.14: Application Problems
  94. 7.15: Solutions to Selected Problems
  95. 08: Introduction to Biomolecules
  96. 8.01: Lipids
  97. 8.02: Proteins
  98. 8.03: Nucleic Acids
  99. 8.04: Carbohydrates
  100. 8.05: Biomolecule Application Problems
  101. 09: Cell Tutorial
  102. 9.01: The Cell- An Overview
  103. 9.02: The Cell- Lipids
  104. 9.03: The Cell - Proteins
  105. 9.04: The Cell- Nucleic Acids
  106. 9.05: The Cell- Carbohydrates
  107. 10: Network Solids
  108. 10.01: A Network Solid - Diamond
  109. 10.02: Other Forms of Carbon
  110. 10.03: Silicates and Silica
  111. 10.04: Aluminosilicates
  112. 10.05: Solutions to Selected Problems
  113. 11: Transition Metal Complexes
  114. 11.01: Introduction
  115. 11.02: Building Blocks- Metal Ions and Ligands in Transition Metal Complexes
  116. 11.03: Electron Counting
  117. 11.04: Chelation
  118. 11.05: Isomers
  119. 11.06: Naming Transition Metal Complexes
  120. 11.07: Geometry in Transition Metal Complexes
  121. 11.08: Solutions for Selected Problems
  122. 12: Macromolecules and Supramolecular Assemblies
  123. 12.01: What are Macromolecules
  124. 12.02: Viscosity
  125. 12.03: Glass Transition
  126. 12.04: Polymer Architecture
  127. 12.05: Morphology and Microphase Separation
  128. 12.06: Polymer Synthesis
  129. 12.07: Molecular Weight
  130. 12.08: Supramolecular Assemblies
  131. 12.09: Solutions for Selected Problems
  132. 13: Molecular Orbital Theory
  133. 13.01: Introductions
  134. 13.02: Wave Behavior and Bonding in the Hydrogren Molecule
  135. 13.03: Molecular Orbitals- Lessons from Dihydrogen
  136. 13.04: Sigma Bonding with p Orbitals
  137. 13.05: Pi Bonding with p Orbitals
  138. 13.06: Assembling the Complete Diagram and Electron Population
  139. 13.07: Experimental Evidence for Molecular Orbital Results
  140. 13.08: Symmetry and Mixing
  141. 13.09: When Different Atoms Bond Together
  142. 13.10: Another Complication in HF- Orbital Mixing
  143. 13.11: Geometry and Orbital Contribution to Bonding
  144. 13.12: Approximations in More Complicated Structures
  145. 13.13: Building a Molecule from Pieces
  146. 13.14: Delocalization
  147. 13.15: Polyenes
  148. 13.16: Delocalization in Aromatics
  149. 13.17: Heteroaromatics
  150. 13.18: Frontier Orbitals
  151. 13.19: Solutions to Selected Problems
  152. 14: Concepts of Acidity
  153. 14.01: General Acidity and Basicity
  154. 14.02: Lewis Bases
  155. 14.03: Lewis Acids
  156. 14.04: Lewis Acid-Base Complexes and Molecular Orbitals
  157. 14.05: Reversibility of the Dative Bond
  158. 14.06: Coordination Complexes
  159. 14.07: Proton as a Common Lewis Acid
  160. 14.08: Proton Transfer from One Basic Site to Another and Molecular Orbital Interactions in Proton Transfers
  161. 14.09: Proton Donor Strength- pKa
  162. 14.10: The Relationship Between Structure and Bronsted-Lowry Acidity
  163. 14.11: Factors Affecting Bronsted-Lowry Acidity- Local Factors
  164. 14.12: Factors affecting Bronsted-Lowry Acidity- Distal Factors
  165. 14.13: Effects on Basicity (Attraction for Proton)
  166. 14.14: The Direction of Proton Transfer
  167. 14.15: Amino Acids and Peptides
  168. 14.16: Relative Conditions and pKa
  169. 14.17: The Meaning of pKa- Product-to-Reactant Ratio and Equilibrium Constant
  170. 14.18: pH and Buffers
  171. 14.19: Application Problems
  172. 14.20: Solutions to Selected Problems