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This set of vocabulary flashcards covers essential reagents and outcome patterns for alkene addition and cleavage reactions based on the lecture notes.
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Hydroboration-Oxidation
A reaction sequence involving BH3. THF followed by H2O2/OH− that results in the anti-Markovnikov addition of water (H and OH) across a double bond with syn stereochemistry.
Oxymercuration-Demercuration
A process using AcOHg,OH and followed by a reducing agent like NaHSO3 to achieve Markovnikov addition of H and OH without carbocation rearrangement.
Acid-Catalyzed Hydration
The addition of water to an alkene in the presence of an acid catalyst such as H2O/H2SO4 to form a Markovnikov alcohol.
Halohydrin Formation
The reaction of an alkene with a halogen in the presence of water (e.g., Cl2/H2O) to add both a halogen atom (Cl) and a hydroxyl group (OH) across the double bond.
Anti-Markovnikov Hydrobromination
The addition of HBr in the presence of peroxides (H2O2) resulting in the bromine atom attaching to the less substituted carbon of the alkene.
Dehydrohalogenation
An elimination reaction using a strong base in alcohol (e.g., KOH,CH3CH2OH) to remove a hydrogen halide from an alkyl halide to form an alkene.
Oxidative Cleavage
A reaction that breaks the carbon-carbon double bond to form carbonyl compounds, such as aldehydes and ketones (e.g., producing H−C=O and O=C−CH3).
Epoxide Ring Opening
A reaction involving an epoxide intermediate treated with aqueous acid (H3O+) in a solvent like CH2Cl2 to yield a 1,2-diol (glycol).