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Fundamental Organic ala Mech

Nguồn ngoài

Fundamental Organic ala Mech

Chemistry
Tác giả
Michael McFavilen
Nhà xuất bản
Chandler-Gilbert Community College
Nguồn
LibreTexts
Giấy phép
CC BY-NC-SA
Ngôn ngữ
EN
Danh mục
Khoa học cơ bản
Đọc trực tuyến Tải PDF (nguồn mở)
Mục lục· 78 mục
  1. 01: Atomic Structure
  2. 1.01: Atomic Structure - The Nucleus
  3. 1.02: Atomic Structure - Orbitals
  4. 1.03: Atomic Structure - Electron Configurations
  5. 02: Molecular Structure
  6. 2.01: Development of Chemical Bonding Theory
  7. 2.02: Describing Chemical Bonds - Valence Bond Theory
  8. 2.03: Drawing Chemical Structures
  9. 2.04: sp Hybrid Orbitals and the Structure of Methane
  10. 2.05: sp Hybrid Orbitals and the Structure of Ethane
  11. 2.06: sp Hybrid Orbitals and the Structure of Ethylene
  12. 2.07: sp Hybrid Orbitals and the Structure of Acetylene
  13. 2.08: Formal Charges
  14. 2.09: Resonance
  15. 2.10: Rules for Resonance Forms
  16. 2.11: Drawing Resonance Forms
  17. 03: Representations of Molecules
  18. 3.01: Drawing Chemical Structures
  19. 3.02: Conformations of Ethane
  20. 3.03: Conformations of Other Alkanes
  21. 3.04: Conformations of Cycloalkanes
  22. 3.4.01: Stability of Cycloalkanes - Ring Strain
  23. 3.4.02: Cis-Trans Isomerism in Cycloalkanes
  24. 3.05: Conformations of Cycloalkanes
  25. 3.5.01: Axial and Equatorial Bonds in Cyclohexane
  26. 3.5.02: Conformations of Monosubstituted Cyclohexanes
  27. 3.5.03: Conformations of Disubstituted Cyclohexanes
  28. 3.5.04: Why This Chapter
  29. 3.5.4.01: Classification of Carbohydrates
  30. 3.5.4.02: Representing Carbohydrate Stereochemistry- Fischer Projections
  31. 3.06: A Review of Isomerism
  32. 3.6.01: Alkanes and Alkane Isomers
  33. 3.6.02: Enantiomers and the Tetrahedral Carbon
  34. 3.6.2.01: The Reason for Handedness in Molecules - Chirality
  35. 3.6.03: Diastereomers
  36. 3.6.04: Meso Compounds
  37. 04: Functional Groups
  38. 4.01: Polar Covalent Bonds - Electronegativity
  39. 4.02: Naming Alkanes
  40. 4.2.01: Alkyl Groups
  41. 4.03: Sequence Rules for Specifying Configuration
  42. 4.04: Naming Alkenes
  43. 4.4.01: Cis-Trans Isomerism in Alkenes
  44. 4.4.02: Alkene Stereochemistry and the EZ Designation
  45. 4.05: Names and Properties of Alkyl Halides
  46. 4.06: Naming Aromatic Compounds
  47. 4.07: Naming Alcohols and Phenols
  48. 4.08: Names and Properties of Ethers
  49. 4.09: Naming Aldehydes and Ketones
  50. 4.10: Naming Carboxylic Acids and Nitriles
  51. 05: Unit 2
  52. 5.01: Functional Groups and Physical Properties
  53. 5.1.01: Polar Covalent Bonds - Electronegativity
  54. 5.1.02: Polar Covalent Bonds - Dipole Moments
  55. 5.1.03: Functional Groups
  56. 5.1.04: Noncovalent Interactions Between Molecules
  57. 5.1.4.01: Properties of Alkanes
  58. 5.1.4.02: Why This Chapter
  59. 5.1.4.03: Waxes Fats and Oils
  60. 5.1.4.04: Soap
  61. 5.02: Reactions overview
  62. 5.2.01: Kinds of Organic Reactions
  63. 5.2.02: Kinds of Organic Reactions
  64. 5.2.03: How Organic Reactions Occur - Mechanisms
  65. 5.2.04: Polar Reactions
  66. 5.2.05: An Example of a Polar Reaction - Addition of HBr to Ethylene
  67. 5.2.06: Using Curved Arrows in Polar Reaction Mechanisms
  68. 5.2.07: Describing a Reaction - Equilibria Rates and Energy Changes
  69. 5.2.08: Describing a Reaction - Energy Diagrams and Transition States
  70. 5.2.09: Describing a Reaction- Intermediates
  71. 5.2.10: Additional Problems
  72. 5.03: Elementary Mechanistic Steps
  73. 5.04: Apply to Acids and Bases
  74. 5.4.01: Acids and Bases - The Brnsted-Lowry Definition
  75. 5.4.02: Acid and Base Strength
  76. 5.4.03: Predicting Acid-Base Reactions from pKa Values
  77. 5.4.04: Organic Acids and Organic Bases
  78. 5.4.05: Acids and Bases - The Lewis Definition