Basic Ideas:
Carbon chains: Straight chains and branched chains, Numbering of chains and branches.
Carbon Rings: Cyclic Molecules, Aromatic Compounds
Types of Organic reactions:
Combustion
Addition
Substitution
Condensation
Oxidation
What is organic chemistry? Carbon compounds.
Methane CH4 Hexane C6 H14
Ethane C2H 6 Heptane C7 H16
Propane C3H 8 Octane C8 H18
Butane C4H10 Nonane C9H20
Pentane C 5 H12 Decane C1 0 H22
Alkanes: Saturated Hydrocarbons
Rules:
Cycloalkanes: Alkenes: Alkynes:
General formula: Cn H2n General formula: Cn H2n General formula:Cn H2n -2
Haloalkanes: Alekanes: Alcohols:
Alkylhalides CnH2n+n “OH” group F (Fluoro), Cl (Chloro), Br (Bromo), I (Iodo)
Other rules:
“Anes” - No double bonds.
“Enes”-At least One double bond.
“Ynes”- At least one triple bond.
“OH”- name ends in “ol”
“ABC rule”- Try to make the chains in Alphabetical order
“Cyclo”- If the chain is connected together it the name must start with Cyclo (If enclosed)
Chain must start where there is most activity
Di, Tri, Tetra – For listing elements when appearing more than once on a chain
Methyl- Single side chain off the main chain
Name side chains by using “yl”- Methyl, ethyl, propyl, etc..
PRIORITY RULES- are a set of rules that allow us to rank certain chemical features of a molecule on a scale of importance. Typically, molecules/groups containing oxygen have a higher priority.
Cyclo groups-
Triangle: Cyclopropane
Square: Cyclobutane
Pentagon: Cyclopentane
Hexagon: Cyclohexane
ISO
Isopropyl- a side chain off of the main chain that has a duel end -<
Isobutyl- \/<
Isopentyl- -/\<
Aromatic Hydrocarbons:
Doesn’t react like an unsaturated molecule.
Ortho-
Meta-
Para-
Toluene-
Phenol-
Addition Vs Substitution: Substitution reactions occur when molecules contain saturated chains (No double or triple bonds) or