General Organic Chemistry Lecture Notes
Topics Covered
- Electron Configurations
- Bonding
- Formal Charge
Line Angle Formula
- Represents molecules using angles and lines.
- Each angle or line end typically represents a carbon atom.
- Example: NAD+ (Nicotinamide adenine dinucleotide) uses line angle formula.
Electron Configurations
- NAD+ as an electron carrier in the body.
- Electrons configurations based on periodic table positions.
- Shells and orbitals:
- 1st shell: 1s orbital (2 electrons)
- 2nd shell: 1s and 3p orbitals (8 electrons total)
- 3rd shell: 1s, 3p, and access to 5d orbitals.
- Orbital shapes:
- S orbitals: spherical, more stable due to volume.
- P orbitals: elongated figure-eight shape.
Electron Configuration in Elements
- Example: Hydrogen (1s1), Helium (1s2)
- Lithium: 1s2 2s1
- Oxygen (neutral): 1s2 2s2 2p4 (2 bonds typically)
- Florine: 1s2 2s2 2p5 (1 bond typically)
- Carbon: typical (1s2 2s2 2p2) vs. true (1s2 2s1 2p3)
Lone Pairs
- Defined as non-bonding electrons in an orbital.
- Example: Oxygen has 2 lone pairs typically.
- Valence shell electrons determine bonding potential.
Types of Bonds
- Covalent Bonds: Formed between nonmetals (e.g., H₂O)
- Polar Covalent: Unequal sharing of electrons (e.g., H₂O)
- Non-polar Covalent: Equal sharing (e.g., Cl₂)
- Ionic Bonds: Formed between metals and nonmetals (e.g., Na⁺ and O²⁻)
Formal Charge
Practice Problems
- Using academic resources like Khan Academy or textbooks is recommended for practice.
These notes summarize the key concepts discussed during the lecture on electron configurations, bonding, and formal charges in organic chemistry.