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What is an Organic Compound? (3)
A molecular compound containing carbon with the exception of CO2, carbonates, carbides and cyanides
due to carbons 4 valence electrons, it makes it the backbone of many complex molecular compounds, often creating long chains and crystal structure
the ability to make long chains make carbon the building block of all life on earth, “carbon based lifeform”
Common uses of fossil fuels (hydrocarbons)
Coal, Oil, and Natural Gas
Alkane Definition
A saturated Hydrocarbon with any single covalent bonds between its carbon atoms
Hydrocarbon Deffinition:
An atom containing only carbon and hydrogen atoms
What is the general formula for alkanes?
CₙH₂ₙ₊₂
Cyclic Alkanes:
A hydrocarbon in which the main structure consists of a chain of carbon atoms joined to form a closed ring
Orientations of Alkanes
Straight Chain Alkane
Cyclic Alkane
Alkyl Groups (3)
An alkyl group is a type of substituent group
One or more carbon atoms that form a branch off the main chain of a hydrocarbon.
Alkyl groups are named with the prefix indicating the number of carbons atoms in the branch, like in your table, however you add a -yl suffix.
Substituent Group
an atom or group that replaces hydrogen in an organic molecule.
Structural Isomerism (2)
Most hydrocarbons with 4 or more carbon atoms exhibit structural isomerism.
Structural isomerism occurs when 2 molecules each have the same number and types of atoms but these atoms are bonded in different ways.
Naming Alkanes (1-20)
1 - methane
2 - ethane
3 - propane
4 - butane
5 - pentane
6 - hexane
7 - heptane
8 - ocatne
9 - nonane
10 - decane
11 - undecane
12 - dodecane
13 - tridecane
14 - tetradecane
15 - pentadecane
16 - hexadecane
17 - heptadecane
18 - octadecane
19 - nondecane
20 - Icosane
Uncommon Alkyl Groups + Alhpa priority
Isopropyl, butyl isobutyl, sec-butyl, tert-butyl
(ensure these are not apart of the longest carbon chain
chose “i” for iso alpha priority
for tert/sec-butyl, ignore the prefix and focus of butyl for alpha priority
iso means
same number
Alkyl Halides + How to name (4)
An alkane in which one or more hydrogen atoms have been
substituted with one or more halogen atoms.
Halides - implies halogen
Add the root of the halogen followed by o when naming
Does the di, tri, tetra change alpha priority?
No you ignore it, ex if u have dimethyl and ethyl, ethyl still comes first
Unsaturated Hydrocarbon:
An unsaturated hydrocarbon is an organic compound, consisting of a carbon and hydrogen, with one more double or triple bonds joining pairs of carbon atoms within the molecules.
Alkene (2)
a hydrocarbon with at least one carbon-carbon double bond
CnH2n
Alkyne (2)
a hydrocarbon that contains at least one carbon-carbon triple bond
CnH2n-2
Alkynes are linear
Naming Alkenes (3)
you have to include alkenes in your parent chain, even if it is not the longest possible change
Alkenes follow the same naming scheme as alkanes, except their ending is changed to “ene” instead of “ane”.
Methene isn’t included as we need a minimum of 2 carbons
Pi bond:
Double bond
2,3,4 pi bond:
di, tri, tetra
Stereoisomers
Molecules that have the same chemical formula and structural backbone, but with a different arrangement of atoms in space
Cis isomer
A stereoisomer in which the groups of interest are located on the same side of a double bond
Trans isomer
a stereoisomer in which groups of interest are located on opposite sides of a double bond
Limitations of Cis/Trans
The cis and trans naming system is limited to simple molecules containing only 1 cis/trans group.
When and when not to include the a in: Pent-3-ene or penta-3-ene etc
Standard: no a pent-3-ene
When you have diene triene etc
Penta-3-diene or penta-3-triene
Why are Alkynes are linear + cis/trans isomers
because carbons only can have 4 bonds. If 3 are already attached to the triple bond, that leaves only 1 single bond to be used on it’s other side.
Alkynes alone do not form cis/trans isomers