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Vocabulary flashcards covering reaction mechanisms, reagents, conditions, and functional group transformations based on the AS Organic Reactions Mind Map.
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Free radical substitution
A reaction where an alkane reacts with Br2 or Cl2 in the presence of UV light to form a halogenoalkane.
Electrophilic addition (Alkene to Halogenoalkane)
A reaction where an alkene reacts with HBr or HCl at room temperature to form a halogenoalkane.
Electrophilic addition / Reduction (Alkene to Alkane)
A reaction where an alkene reacts with H2 using a nickel catalyst or platinum to form an alkane.
Alkene Oxidation to Diol
A reaction where an alkene reacts with cold, dilute H+/KMnO4 at room temperature to form a diol.
Nucleophilic substitution (Halogenoalkane to Alcohol)
A reaction where a halogenoalkane is heated under reflux with aqueous KOH to form an alcohol.
Elimination (Halogenoalkane to Alkene)
A reaction where a halogenoalkane is heated under reflux with alcoholic KOH to form an alkene.
Dehydration (Alcohol to Alkene)
An elimination reaction where an alcohol is heated with concentrated H2SO4 to form an alkene.
Partial Oxidation of Primary Alcohol
A reaction where a primary alcohol is gently heated and distilled with K2Cr2O7/H+ to form an aldehyde.
Complete Oxidation of Primary Alcohol
A reaction where a primary alcohol or aldehyde is heated under reflux with excess oxidising agent (K2Cr2O7/H+) to form a carboxylic acid, accompanied by a color change from orange to green.
Oxidation of Secondary Alcohol
A reaction where a secondary alcohol is heated under reflux with K2Cr2O7/H+ to form a ketone.
Nucleophilic Addition (Hydroxynitrile formation)
A reaction where an aldehyde or ketone reacts with HCN in the presence of a KCN catalyst under heat to form a hydroxynitrile.
Nucleophilic Substitution (Halogenoalkane to Nitrile)
A reaction where a halogenoalkane is heated with CN− in ethanol to produce a nitrile.
Nucleophilic Substitution (Halogenoalkane to Amine)
A reaction where a halogenoalkane is heated under pressure with alcoholic NH3 to form an amine.
Reduction of Nitrile
A reaction where a nitrile is reduced using LiAlH4 to form an amine.
Esterification
A condensation reaction where a carboxylic acid is heated with an alcohol in the presence of concentrated H2SO4 to form an ester.
Acyl Chloride Reaction with Ammonia
A nucleophilic addition-elimination reaction occurring at room temperature between an acyl chloride and NH3 to produce a primary amide.
Acyl Chloride Reaction with Primary Amine
A nucleophilic addition-elimination reaction occurring at room temperature between an acyl chloride and a primary amine to produce a secondary amide.
Acyl Chloride Reaction with Secondary Amine
A nucleophilic addition-elimination reaction occurring at room temperature between an acyl chloride and a secondary amine to produce a tertiary amide.
Hydrolysis of Acyl Chloride
A reaction where an acyl chloride reacts with H2O at room temperature to form a carboxylic acid.
Triiodomethane (Iodoform) Test
A test for methyl ketones or methyl alcohols using alkaline I2 (aq), producing a yellow precipitate of triiodomethane (CHI3).