Description:

Lec 1:

Basic Nomenclature

1. Prefixes
2. Functional group prefixes
3. Example

Lec 2:

1. Orbitals
2. Stereochemistry
3. R vs S

Lec 3:

1. Orbitals
2. Hybridization
3. Degrees of Unsaturation

Lec 4:

1. Bond angles trends
2. Geometry
3. Bond Length trends 
4. Bond Strength trends

Lec 5:

1. Distinction between types of isomers
2. Geometric
3. Stereoisomers
4. Constitutional
5. Optical
6. Diasteromer, Enantiomer

Lec 6:

1. Enantiomer
2. Diasteromer
3. Anomer
4. Epimer

Lec 7:

1. Properties of Alkanes
2. Boiling Point
3. Hydrogen Bonding
4. Stability
5. Reactivity

Lec 8:

1. Acidity Trends
2. Strong acids
3. Strong bases

Lec 9:

1. Free Radical Halogenation

Lec 10:

1. SN1 vs SN2
2. Mechanism
3. Products
4. Properties

Lec 11:

E1 vs E2

Lec 12:

SN1 vs SN2 Reaction Overview

Lec 13:

Alkene Reactions

1. Bromination
2. H20 Addition
3. Oxymerc-Demurcuration
4. Markovnikov Addition

Lec 14:

AntiMarkovnikov Reactions

Lec 15:

Aromatic Compounds

1. Huckel’s Rule
2. Aromatic vs Nonaromatic

Lec 16:

Aldehyde and Ketone Reactions

1. Alcohol Additions
2. Reductions
3. Oxidations
4. Grignard Reaction

Lec 17:

More Aldehyde and Ketone Reactions

1. Alcohol Addition
2. Amine Addition
3. Aldol Condensation

Lec 18:

Diels Alder Reaction