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Vocabulary based on the C3.5 organic chemistry reaction scheme, covering functional groups, reagents, and reaction types.
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1° Amine
An organic functional group that turns red litmus paper blue.
Acid chloride
A highly reactive functional group that undergoes a violent reaction with water.
Aldehyde
A carbonyl compound formed by the oxidation of a primary alcohol under cold conditions with Cr2O72−/H+; it shows a positive reaction to Tollens' and Benedict's reagents.
Ketone
A carbonyl compound formed by the oxidation of a secondary alcohol; it shows no reaction to Tollens' or Benedict's reagents.
NaBH4
A reducing agent used to convert aldehydes and ketones back into primary and secondary alcohols.
Cr2O72−/H+ (reflux)
An oxidizing agent and condition used to convert primary alcohols or aldehydes into carboxylic acids, or secondary alcohols into ketones.
MnO4−/H+
An alternative oxidant used for the oxidation of alcohols or aldehydes.
PCl3, PCl5, or SO3Cl2 (reflux)
Reagents used to substitute a hydroxyl group with a chlorine atom to form haloalkanes or acid chlorides.
Alc.KOH (reflux)
Reagent and condition used to convert a haloalkane into an alkene via an elimination reaction.
KOH(aq) (reflux)
Reagent and condition used to convert a haloalkane into an alcohol via a substitution reaction.
Conc.H2SO4 (heat)
A strong acid used to catalyze the dehydration of an alcohol to an alkene or the esterification of a carboxylic acid and alcohol.
Ester
A compound formed from the condensation of a carboxylic acid (or acid chloride) and an alcohol; it can be hydrolyzed back using H2O/H+ or NaOH (heat).
Amide
A functional group formed by the reaction of an acid chloride with NH3 or an amine.
Condensation Polymerisation
A polymerization process where monomers like di-alcohols and di-carboxylic acids join together, releasing H2O to form polyesters.
Dipeptide
A molecule formed by the condensation reaction between two amino acids.
Carboxylate ion
The conjugate base of a carboxylic acid, often formed as a salt (NH4+) when a carboxylic acid reacts with a base.
H2 with Pt or Ni catalyst
Conditions used for the hydrogenation reaction to convert an alkene into an alkane.
NH3(alc) or NH3 in ethanol
Reagent and solvent used to convert a haloalkane into a primary amine.
H2O/H+ (heat)
Acidic hydrolysis conditions used to break down esters, amides, or poluners into their constituent carboxylic acids and alcohols/amines.
Br2 / Cl2
Halogens used to convert alkanes to haloalkanes (slow reaction) or alkenes to dihaloalkanes (fast reaction).