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Aldehydes and Ketones

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

If C=O is on the end of the chain it is…?

Back (Answer)

An aldehyde

#2
Front (Question)

If C=O is in the middle of the chain it is..?

Back (Answer)

A ketone

#3
Front (Question)

Name ending for aldehydes?

Back (Answer)

-al.

#4
Front (Question)

Name ending for ketones?

Back (Answer)

-one.

#5
Front (Question)

What forces are present in aldehydes and ketones?

Back (Answer)

Van der waals. Permanent dipole forces.

#6
Front (Question)

Can aldehydes and ketones form hydrogen bonds?

Back (Answer)

Not with themselves.

#7
Front (Question)

Why are smaller carbonyls soluble in water?

Back (Answer)

They can form hydrogen bonds with water.

#8
Front (Question)

Describe the polar bond in C=O.

Back (Answer)

It is polarised because O is more electronegative than C. The positive carbon atom attracts nucleophiles.

#9
Front (Question)

Why don’t aldehydes and ketones undergo addition reactions easily?

Back (Answer)

The C=O bond is stronger than the C=C bond which is why electrophiles are attracted to the C=C.

#10
Front (Question)

What oxidising agent oxidises alcohols and aldehydes?

Back (Answer)

Potassium dichromate

#11
Front (Question)

What can a primary alcohol be oxidised into?

Back (Answer)

Aldehyde then aldehydes can be oxidised into carboxylic acids.

#12
Front (Question)

What can a secondary alcohol be oxidised into?

Back (Answer)

A ketone only since ketones can’t be oxidised.

#13
Front (Question)

What can a tertiary alcohol be oxidised into?

Back (Answer)

Nothing

#14
Front (Question)

What reagents are needed for the oxidation of aldehydes into carboxylic acids? What condition is needed?

Back (Answer)

Dilute sulfuric acid and potassium dichromate solution. Heat under reflux.

#15
Front (Question)

What is seen in the oxidation of aldehydes into carboxylic acids?

Back (Answer)

Turns from orange to green.

#16
Front (Question)

What can be used to test for aldehydes?

Back (Answer)

Tollens’ Reagent Fehling’s Solution

#17
Front (Question)

What condition is needed for Tollens’ Reagent? What happens in the reaction? What can you observe?

Back (Answer)

1) Heat gently 2) Aldehydes are oxidised into a carboxylic acid. 3) Silver mirror forms.

#18
Front (Question)

What condition is needed for Fehling’s solution? What happens in the reaction? What can you observe?

Back (Answer)

1) Heat gently 2) Aldehydes are oxidised into a carboxylic acid. 3) Turns from blue to brick red precipitate.

#19
Front (Question)

Which reducing agents reduce carbonyls into alcohols?

Back (Answer)

LiAlH4 NaBH4

#20
Front (Question)

What is NaBH4?

Back (Answer)

Sodium Tetrahydridoborate.

#21
Front (Question)

What is LiAlH4?

Back (Answer)

Lithium Tetrahydridoaluminate.

#22
Front (Question)

What conditions are needed for the reduction of carbonyls?

Back (Answer)

Room temperature and pressure

#23
Front (Question)

What are aldehydes reduced into?

Back (Answer)

Primary alcohols

#24
Front (Question)

What are ketones reduced into?

Back (Answer)

Secondary alcohols