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Organizing Organic Chemistry Basics
Ch. 1: Basics of Chemistry
이즈그리민(izgrimean)
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Jeongbin Park
|
2024-05-31
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izgrimean 페이퍼
Creative Commons
Getting Started
Ch. 1: Basics of Chemistry
Ch. 1: Basics of Chemistry
1. What is Chemistry?
2. Grammar of Chemical Formulas
3. Chemical Reaction Equations
Ch. 2: Classical Atomic Theory
Ch 2: Classical Atomic Theory
1. History of Atomic Models
2. Classical Atomic Model
3. Classical Molecular Model
4. Drawing Molecular Structures
5. Formal Charge
Ch. 3: VSEPR
Ch. 3: VSEPR
1. VSEPR
2. Dipole Moment
Ch. 4: Orbital Theory
Ch. 4: Orbital Theory
1. Orbital Atomic Model
2. Multielectron Atom
3. Atomic Bonding Theory
4. Molecular Orbital Theory
Ch. 5: Basics of Organic Chemistry
Ch. 5: Basics of Organic Chemistry
1. What is Organic Chemistry?
2. Organic Chemistry Structural Formulas
3. Bond Length and Bond Strength
4. Resonance Structures
5. Acid-Base Theory
Ch. 6: Lewis Structures
Ch. 6: Lewis Structures
1. How to Draw Lewis Structures
2. Rules of Lewis Structures
3. Complicated Lewis Structures
Ch. 7: Nomenclature
Ch. 7: Nomenclature
1. Ionic Bond Nomenclature
2. Covalent Bond Nomenclature
3. Organic Chemistry Nomenclature
4. Linear Alkane Nomenclature
5. Cyclic Alkane Nomenclature
6. Complex Cyclic Alkane Nomenclature
7. Acyclic Alkene and Alkyne Nomenclature
8. Cyclic Alkene and Alkyne Nomenclature
9. Aromatic Compound Nomenclature
10. Alcohol Nomenclature
11. Ether Nomenclature
12. Epoxide Nomenclature
13. Aldehyde and Ketone Nomenclature
14. Carboxylic Acid and Analogues Nomenclature
15. Amine and Analogues Nomenclature
16. Python Code for Nomenclature
Ch. 8: Alkanes
Ch. 8: Alkanes
1. Overview
2. Nomenclature
3. Degree of Unsaturation
4. Physical Properties of Alkanes
5. Conformational Isomers (Conformers)
6. Cyclohexane
7. Alkane Reactions
Ch. 9: Cycloalkane and Cycloalkene
Ch. 9: Cycloalkane and Cycloalkene
1. Structure of Cycloalkanes
2. Structure of Cycloalkenes
Ch. 10: Stereochemistry
Ch. 10: Stereochemistry
1. Isomers
2. E-Z Nomenclature
3. Mirror-Image Isomers
4. Optical activity
5. Mesocompounds and racemic mixtures
6. Coordination Compound Isomers
7. Bürgi–Dunitz trajectory