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Functional Groups
a Functional Group is a group of atoms within a molecule that has a characteristic chemical behavior.
R is a shorthand notation that could mean
Any Carbon chain or any Hydrogen.
Condensed Formula
CH3CH2CH3

Kekule Structure
(see image)

Skeletal Structure (Line Diagram)
(see image) each end of a line (unless otherwise like the Hydrogen or Oxygen) is a Carbon, the lines represent single bonds. Hydrogens are NOT USUALLY drawn (there are exceptions).

HydroCarbon Groups
Alkane, Alkene, Alkyne and Aromatic Ring (Arene)
Alkane
C-C single bond (ane ending)

Names of Alkanes (From having 1 Carbon single bond chain - 10 Carbon single bond Chains
Carbon: Methane
Carbons: Ethane
Carbons: Propane
Carbons: Butane
Carbons: Pentane
Carbons: Hexane
Carbons: Heptane
Carbons: Octane
Carbons: Nonane
Carbons: Decane
Alkene
C=C double bond (ene sufix)

Alkyne
C C triple bond (yne suffix)

Aromatic Ring (Arene)
ring with double bonds

Cycloalkane
End Carbon comes back to First carbon, single bonds.

Primary Carbon
Attached to one other Carbon (i)
Secondary Carbon
Carbon attached to other Carbons, 2°
Tertiary Carbon
Attached to 3 other Carbons, 3°
Oxygen Groups
(Carbon-Oxygen, Carbon single bonded to Oxygen) Alcohol and Ether
Alcohol
sp3 Carbon with bonded to OH (ol suffix)

Ether
C-O-C Oxygen single bonded to Carbon on both ends.

Carbonyl Groups
(Carbon=Oxygen, Carbon double bonded to Oxygen with something else attached): CEAAAK (sea sick, you yack, sea triple yack)
Carboxylic Acid
Ester
Acid Chloride
Aldehyde
Amide
Ketone
Carboxylic Acid
Carbonyl bonded to OH, suffix oic acid (OH base to mix with ACID)

Ester
Carbonyl bonded to -O-C, suffix oate (Ester easter, O looks like an easter egg)

Acid Chloride
Carbonyl attached to Chlorine, suffix oyl chloride

Aldehyde
(Oxygen=C-H) carbonyl attached to H, suffix al (hyde has an H, hydrogen)

Amide
Carbonyl attached to NH2 , suffix amide

Ketone
Carbonyl attached to 2 carbons on both sides, suffix one

Amine
Carbon single bonded to NH2 (it’s like amide, without the oxygen double bond).

Alkyl Group
Comes specifically from alkanes. It happens by removing ONE hydrogen so that it is readily available to attach to something else. When a Hydrogen is removed from an alkane, you add an yl suffix. EX: Methane is CH4, when you remove a Hydrogen, CH3 it becomes methyl. If you have an Ethane, C-C (CH3CH3) and remove one Hydrogen (CH3CH2) it becomes ethyl.

IUPAC Naming
Find the Parent Chain: LONGEST continuous Carbon chain (EX: 4 Carbons, Butane) this becomes your BASE NAME.
Identify the highest priority functional group, this will give your SUFFIX.
Number the chain so that it gives the lowest possible numbers to your alkyl groups
Identify and name your alkyl groups
Assign the numbers to your alkyl groups by where they are placed. If you have two groups on the same carbon, write the number twice. (Numbers are separated from words through -, 2,2-dimethylpropane).
Use prefixes based on how many of the same group you have. EX: if you have two methyl’s, it’s dimethyl
Arrange your name alphabetically, (ignore prefixes like di or tri) EX: Methyl and Bromo, B comes before M, 2-bromo-3-methylpentane
If you have a double bond, number the double bond based on the lowest number where it starts.
When you have more than one functional group, the highest priority becomes the suffix, but the second priority functional group will give you your prefix.
EX: H₂NCH₂CH₂OH
Functional groups:
Alcohol (-OH)
Amine (-NH₂)
Alcohol has higher priority.
Name: 2-aminoethan-1-ol
The amine is named as the prefix amino-.
Isopropyl
3 Carbon chain, propane, remove a Hydrogen, propyl, when it’s attached in the middle, it is an isopropyl.

Nitrile
Carbon triple bonded to Nitrogen

Thiol
Sulfur-Hydrogen, sulfur single bonded to Hydrogen

Sulfide
C-S-C Sulfur single bonded to Carbon on both sides. If you have 2 sulfurs, C-S-S-C disulfide
Flourine attached
Flouro
Chlorine attached
Chloro
Bromine attached
Bromo
Iodione attached
Iodo
When writing Chemical Formula
written as C,H, then everything else in alphabetical order.