3.3.8 Aldehydes and ketones Flashcards
What do aldehydes produce when oxidised?
Carboxylic acids
How do you make Tollens reagent? (3)
- Silver nitrate
- Drops of NaOH
- Drops of ammonia
Tollens test + postive result
- Tollens + water bath.
- Silver mirror
Fehling’s test result
Changes from blue to brick red precipitate
Why does Fehling’s test work?
- Aldehyde can reduce Cu2+ to Cu+
How do you get primary/secondary alcohols?
Reduce aldehyde/ketone using NaBH4
Reduction of Aldehydes and Ketones mechanism name
Nucleophilic addition reaction (diagram)
KCN + aldehyde/ketone mechanism
Same as reduction, except with CN instead of the first H+ added (diagram)
Why is KCN used instead of HCN?
HCN is too toxic, and so KCN disassociates better
Remember KCN should be aqueous
H+ H- mechanism nuance
- C=C = electron rich, repels H-
- H- is attracted to C+
Dehydration of alcohols conditions
Concentrated H2SO4 + reflux
How to obtain pure crystals of ketone (4)
- Filter
- Dissolve in small volume of hot solvent
- Leave to cool, filter
- Wash with cold water and leave to dry