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Flashcards covering key reactions and properties of alkenes and haloalkanes.
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Dihydroxylation
A reaction where osmium tetroxide adds to alkenes to introduce two -OH groups.
OsO4
Osmium tetroxide, a reagent used in the dihydroxylation of alkenes.
1,2-diol
A diol where two hydroxyl (-OH) groups are added to the first and second carbons.
Glycol
Another name for a 1,2-diol.
N-methylmorpholine N-oxide (NMO)
An oxidizing agent used in Upjohn dihydroxylation.
Ozonolysis
A reaction that uses ozone to cleave a C=C double bond, producing carbonyl compounds.
Molozonide
An intermediate formed in the ozonolysis reaction.
Ozonide
A compound formed when a molozonide rearranges.
Chain reaction
A reaction where the products initiate further reactions, typical of radical processes.
Initiation step
The first step in a chain reaction where radicals are formed.
Propagation step
The steps in a chain reaction that produce new radicals and continue the reaction.
Chain termination
The step in a chain reaction where radicals combine to form stable products.
Regioselectivity
Preference of a reaction to occur at one location over others in a molecular structure.
Stereochemistry of radical halogenation
The creation of a racemic mixture resulting from halogenation where a chiral center is formed.
Allylic radical
A radical formed on a carbon next to a C=C double bond, stabilized by resonance.
N-bromosuccinimide (NBS)
A reagent that can promote allylic bromination under radical conditions.
Non-Markovnikov addition
Addition of HX to an alkene in which the hydrogen adds to the least substituted carbon.
Autoxidation
A reaction that requires oxygen to oxidize an organic compound, usually initiated by a radical.
R-X
The general formula for haloalkanes, where R is an alkyl group and X is a halogen.
Chlorofluorocarbons (CFCs)
Compounds that were once used as refrigerants and propellants, harmful to the ozone layer.
PFASs (Per- and polyfluoroalkyl substances)
Organic compounds where hydrogen is replaced by fluorine, persistent in the environment.