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11 Cards in this Set

  • Front
  • Back
Define the term structural formula.
Shows the unique arrangement of atoms in a molecule in a simplified form, without showing all the bonds.
Define the carbon bond in alkanes and alkenes?
> -enes have a double carbon bond,
> -anes do not
Define how many carbons are in alkanes and alkenes?
>MEPB
1C = Meth
2C = Eth
3C = Prop
4C = But
5C = Pent
6C = Hex
7C = Hep
8C = Oct
9C = Non
10 = Dec
Define the prefixes used in organic chemistry to locate branches.
Prefixes are added to describe changes that have been made to root molecule.
What is a functional group?
An atom or group of atoms in an organic molecule that are responsible for the characteristic of that molecule.
Define the 6 suffixes used in organic chemistry.
>Alkane= -ane as in methane
>Alkene-= -ene as in methene
>Halogenalkanes= fluor-, chloro-, bromo-, iodo-,
>Alcohols (-OH) = -ol as in methanol, CH3OH
>Aldehydes (-CHO) = -al as in ethanal CH3CHO
>Ketones (-COR) = -one as in propanone CH3COCH3
>Carboxylic acids (-COOH) = -oic acid as in ethanoic acid CH3COOH
What are structural isomers?
Molecules that have the same molecular formula but whose atoms are arranged differently.
Define an homologous series.
A set of organic compounds with the same functional group. The compounds differ in the length of their hydrocarbon chains.
What are the three ways in which structural isomerism can occur?
>Positional isomerism - same functional group attached to main chain at different points
>Functional group isomerism - functional groups that are different
>Chain isomerism - different arrangement of hydrocarbon chain (branching)
Stereoisomers
Compounds with the same structural formula but have a different arrangement in space
Two types of stereoisomerism
Z-isomers= 'cis' isomer, where non-hydrogen groups are on the same side of molecule

E-isomers= 'trans' isomer, where non-hydrogen groups are on opposite of molecule