Back to marketplace

3.8 Aldehydes and Ketones

No description yet. This curated deck is ready for daily study.

Total cards: 24•Content version: v3•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

What is the carbonyl group?

Back (Answer)

C=O

#2
Front (Question)

What is the functional group and general formula for an aldehyde?

Back (Answer)

RCHO (C double bonded to O, single bond to H and R)

#3
Front (Question)

What is the functional group for a ketone?

Back (Answer)

RCOR’ (C double bonded to O)

#4
Front (Question)

How do you name aldehydes?

Back (Answer)

-al suffix (C=O is on the end of a chain)

#5
Front (Question)

How do you name ketones

Back (Answer)

-one suffix (designate number for which carbon C=O is on)

#6
Front (Question)

What kind of intermolecular forces do molecules with the carbonyl group have? Why?

Back (Answer)

Permanent dipole-dipole due to the polar C=O bond (O is delta -)

#7
Front (Question)

How soluble are they in water? What influences solubility?

Back (Answer)

Yes forms hydrogen bonds between water molecules and oxygen of C=O. As C chain length increases, solubility decreases

#8
Front (Question)

Which bond in carbonyl compounds is usually involved in reactions? Why?

Back (Answer)

C=O, due to the polarity of the bond (large difference in electronegativity between C and O)

#9
Front (Question)

What is the strongest bond in carbonyl compounds?

Back (Answer)

C=O

#10
Front (Question)

Draw a mechanism for the nucleophilic addition of a carbonyl compound, using :Nu- to represent the nucleophile

Back (Answer)

Slide 21

#11
Front (Question)

Draw a mechanism for the nucleophilic addition of HCN to a carbonyl compound

Back (Answer)

Slide 23

#12
Front (Question)

Why is the addition of HCN important

Back (Answer)

Increases the length of the carbon chain by one carbon atom - very useful

#13
Front (Question)

Will the product of HCN added to a carbonyl compound have optical isomers? Why?

Back (Answer)

Yes they will. In the aldehyde/ketone, the carbonyl carbon is planar, so the :CN- can attack from either above or below, forming two enantiomer

#14
Front (Question)

What is the name of the product when HCN is added to a carbonyl compound?

Back (Answer)

Hydroxynitriles (have OH and CN groups)

#15
Front (Question)

What is Fehling’s solution? What colour is it?

Back (Answer)

Copper complex ions, blue

#16
Front (Question)

What happens when an aldehyde is added to Fehling’s solution?

Back (Answer)

Reduced to Cu+ ions —> colour change to brick red ppt

#17
Front (Question)

What happens when a ketone is added to Fehling’s solution?

Back (Answer)

No visible change —> stays blue

#18
Front (Question)

What is in tollens’ reagent?

Back (Answer)

Silver complex ions, colourless solution

#19
Front (Question)

What happens when an aldehyde is added to tollen’s reagent?

Back (Answer)

Silver mirror forms as Ag+ reduced to Ag(s)

#20
Front (Question)

What happens when a ketone is added to tollen’s reagent?

Back (Answer)

No visible change

#21
Front (Question)

What is another oxidising agent for alcohols and aldehydes? What change in colour does this undergo?

Back (Answer)

Acidified potassium dichromate (VI) - H2SO4 and K2Cr2O7. Colour change from orange to green

#22
Front (Question)

What is a reducing agent for aldehydes and ketones? What ions does this release in solution?

Back (Answer)

NaBH4 (sodium tetrahydridoborate (III)), releases an H- ion

#23
Front (Question)

Draw and name a mechanism for the reduction of an aldehyde

Back (Answer)

Slide 47

#24
Front (Question)

Write an equation for the reduction of pentan-2-one and for 3xmethylbutanal

Back (Answer)