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Vocabulary flashcards covering the basics of organic chemistry, including naming conventions for alkanes, alkenes, and alkynes, isomerism, and properties of hydrocarbon chains.
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Organic molecules
Carbon-based molecules.
Organic chemistry
The chemistry of carbon-based molecules.
Properties of organic molecules
Stability composed of stable C−C covalent bonds, defined molecular structures, and defined three-dimensional shapes.
Methane
A hydrocarbon with four single covalent bonds and a tetrahedral shape.
Hydrocarbons
Molecules composed of carbon and hydrogen where each carbon atom forms 4 chemical bonds.
Saturated hydrocarbon
A hydrocarbon where all C−C bonds are single bonds and the molecule contains the maximum number of H-atoms.
Alkanes
Another name for saturated hydrocarbons, identified by the suffix "-ane".
Meth-
Prefix indicating 1 Carbon atom.
Eth-
Prefix indicating 2 Carbon atoms.
Prop-
Prefix indicating 3 Carbon atoms.
But-
Prefix indicating 4 Carbon atoms.
Pent-
Prefix indicating 5 Carbon atoms.
Hex-
Prefix indicating 6 Carbon atoms.
Hept-
Prefix indicating 7 Carbon atoms.
Oct-
Prefix indicating 8 Carbon atoms.
Non-
Prefix indicating 9 Carbon atoms.
Dec-
Prefix indicating 10 Carbon atoms.
Undec-
Prefix indicating 11 Carbon atoms.
Dodec-
Prefix indicating 12 Carbon atoms.
Normal alkanes
Alkanes consisting of continuous chains of carbon atoms.
Branched alkanes
Alkanes that are not continuous chains and contain side chains or branches.
Parent chain
The longest continuous chain of carbons in a hydrocarbon used for naming.
Structural isomers
Molecules with the same chemical formulas but different molecular structures and connectivity.
Methyl group
A one-carbon branch represented as CH3−.
Ethyl group
A two-carbon branch represented as CH3CH2−.
Halogen branch naming
Dropping the "-ine" suffix and adding "-o", such as Bromine becoming Bromo.
Cycloalkane
A hydrocarbon chain that has been joined to make a ring, resulting in the loss of two hydrogen atoms compared to the straight chain.
Angle (ring) strain
Strain resulting from the compression of internal bond angles, being greatest in cyclopropane (60∘) and eliminated in cyclohexane.
Alkenes
Hydrocarbons containing at least one carbon-carbon double bond, identified by the suffix "-ene".
Alkynes
Hydrocarbons containing at least one carbon-carbon triple bond, identified by the suffix "-yne".
Alkane General Formula
CnH2n+2
Alkene General Formula
CnH2n
Alkyne General Formula
CnH2n−2
Cis isomer
An isomer where substituents are on the same side of a double bond.
Trans isomer
An isomer where substituents are on opposite sides of a double bond.