In aldehydes, the carbonyl group has a hydrogen atom attached to it together with either:
a second hydrogen atom or, more commonly, a hydrocarbon group which might be an alkyl group or one containing a benzene ring
a third hydrogen atom with another R group
one hydrogen atom with two R groups
How do you make aldehydes?
by oxidising primary alcohols
by a reflux experiment
By heating up a ketone
Which is an aldehyde?
Are aldehydes soluble?
Yes
No
Only short chain aldehydes
Which statement is true?
An aldehyde differs from a ketone by having a hydrogen atom attached to the carbonyl group. This makes the aldehydes very easy to oxidise.
An aldehyde and a ketone are very similar and act in the same way when you try to oxidise them
Ketones have that hydrogen atom and are not resistant to oxidation.
Aldehydes are...
usually more reactive toward nucleophilic substitutions than ketones because of both steric and electronic effects.
atomically extremely heavy
do not oxidise