Chapter 1:
- Covalent bonds
- Lewis Dot Structures
- Octet rule
- Double bonds
- Triple bonds
- Polar covalent
bonds
- Formal charge
- Structural formulas
- Constitutional
formulas
- Resonance
- Shapes of molecules
- VSEPR
- Acids and bases
- Arrhenius model
- acid
H+ producer
- base
OH- producer
- Brønsted-Lowry
model
- acid
proton donor
- base
proton acceptor
- Lewis acid-base
model
- acid
electron pair acceptor
- base
electron pair donor
- Conjugate acid
- Conjugate base
- pKa
(- log [Ka] )
- HCl
~ 1
- HC2H3O2
~ 4-5
- HNH3+
~ 9-10
- HOH
~ 15.7
- HNH2
~ 36
- HC
~ 60
- Inductive effects
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Chapter 2:
- Hydrocarbons
- Aliphatic hydrocarbons
- Aromatic hydrocarbons
- Valence bond
model
- Lewis Dot Structures
- Molecular orbital
model
- Sigma (σ
) bond
- Pi (π) bond
- Orbital hybridization
(sp3, sp2, sp)
- Alkane nomenclature
- Isomeric alkanes
- IUPAC nomenclature
- Alkyl groups
(see below)
- Types of carbons:
- Primary (1o)
- Secondary
(2o)
- Tertiary
(3o)
- Quarternary
(4o)
- Cycloalkane nomenclature
- Physical properties
- Intermolecular
forces
- van der Waals
forces
- Heat of combustion
(enthalpy)
- Oxidation number
Alkyl groups
you should know:
- methyl, ethyl,
propyl, butyl, pentyl
- isopropyl (1-methylethyl)
- isobutyl (2-methylpropyl)
- sec-butyl (1-methylpropyl)
- t-butyl (1,1-dimethylethyl)
- isopentyl (3-methylbutyl)
- neopentyl (2,2-dimethylpropyl)
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Chapter 3:
- Conformations
- Staggered conformation
- Eclipsed conformation
- anti conformation
- Gauche conformation
- Torsional strain
- Steric strain
- Activation energy
(Ea)
- van der Waals
strain
- Steric hindrance
- Carbon-carbon
bond rotation
- Angle strain
- Torsional strain
- Cyclopentane
- Cyclohexane
- Axial position
- Equatorial position
- 1,3-diaxial repulsions
- Stereoisomers
(geometric isomers)
- Polycyclic rings
- Spirocyclic compounds
- Polycyclic compounds
- Heterocyclic
compounds
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