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Alkane to haloalkane
Through a substitution reaction with the halogen under UV conditions
Alkene to alkane
Through an addition/reduction reaction with hydrogen and a catalyst
Alkene to haloalkane
Through an addition reaction with a hydrogen and halogen (e.g., HCL)
Alkene to dihaloalkane
Through an addition with a dihalogen molecule (e.g., Cl2)
Alkene to Alcohol
Through an addition reaction with heat, H2O and a catalyst
Alkene to Polymer
Through an addition reaction with a catalyst, heat and pressure
Haloalkane to Alcohol
Through a substitution reaction with reflux and NaOH(aq)
Haloalkane to Amine
Through a substitution reaction with NH3 and conc
Haloalkane to Nitrile
Through a substitution reaction with KCN and reflux
Haloalkane to Alkene
Through an elimination reaction with NaOH and reflux
Primary Alcohol to Aldehyde
Through an oxidation reaction with H/MnO4 and heat
Primary Alcohol to Carboxylic Acid
Through a second oxidation reaction (alcohol to aldehyde to carboxylic acid) with H/Cr2O7 and heat for longer
Secondary Alcohol to Ketone
Through an oxidation reaction with H/MnO4 or H/Cr2O7
Carboxylic Acid to Ester
Through a condensation or esterification reaction with an alcohol and heat
Carboxylic Acid to Salt
Through a neutralisation reaction with a base
Amine to Amide
A condensation reaction with a carboxylic acid
Amine to Salt
A neutralisation reaction with an acid
Nitrile to Amine
A reduction/addition reaction with a H2/Ni catalyst and heat
How are alkanes distinguished from alkenes?
When using Br2, alkenes turn the red colourless
How do you determine the level of alcohols?
Through the number/products of oxidation. Primary alcohols oxidise twice, secondary once and tertiary null.
How to determine between an aldehyde and ketone?
Because aldehydes oxidise and ketones don't, aldehydes turn orange dichromate green and purple manganate pale pink
Markovnikov's Rule
When an unsymmetrical reagent is added to an unsymmetrical alkene, the H goes to the C's that has the most H's