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Unit 4.4 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)

What can oxidising primary/secondary alcohols give u?

Back (Answer)

Aldehydes or ketones

#2
Front (Question)

What’s the oxidising agent used for the oxidisation of primary/secondary alcohols? (Either one)

Back (Answer)

• Acidified potassium dichromate (VI) • Acidified potassium manganate (VII)

#3
Front (Question)

Which alcohol being oxidised creates the formation of an aldehyde?

Back (Answer)

Primary alcohols

#4
Front (Question)

Show me the equation of the formation of an aldehyde from the oxidisation of primary alcohols (Whiteboard needed)

Back (Answer)

Where’s your whiteboard?

#5
Front (Question)

Which alcohol being oxidised creates the formation of a ketone?

Back (Answer)

Secondary alcohols

#6
Front (Question)

Show me the equation of the formation of a ketone from the oxidisation of secondary alcohols (Whiteboard needed)

Back (Answer)

Where’s your whiteboard?

#7
Front (Question)

What are the 2 reagents used to distinguish between aldehydes and ketones

Back (Answer)

• Tollen’s reagent • Fehling’s reagent

#8
Front (Question)

What consists of Tollen’s reagent? (2 things + 1 what?)

Back (Answer)

• Mild oxidising agents such as Ag+ • Usually an ammoniacal solution of silver nitrate • contains diamminesilver(I) ion, [(NH302Ag]+)

#9
Front (Question)

What does Tollen’s reagent oxidise?

Back (Answer)

The aldehyde

#10
Front (Question)

What observations are there from aldehyde with Tollen’s reagent? and how?

Back (Answer)

• Silver mirror forms • Oxidised further

#11
Front (Question)

What does Tollen’s reagent not oxidise?

Back (Answer)

The ketone

#12
Front (Question)

What observations are there from ketone with Tollen’s reagent? and how?

Back (Answer)

• No observable change or goes black • Cannot be oxidised further

#13
Front (Question)

Equation for aldehyde with Tollen’s reagent?

Back (Answer)

Get your whiteboard Carboxylic acid formed i think

#14
Front (Question)

Equation for ketone with Tollen’s reagent?

Back (Answer)

It don’t work

#15
Front (Question)

What is step 1 of Tollen’s reagent experiment (Method)

Back (Answer)

• Add 1cm (depth) of silver nitrate to a boiling tube

#16
Front (Question)

What is step 2 of Tollen’s reagent experiment (Method) (2-way)

Back (Answer)

• Add sodium hydroxide dropwise • until a brown ppt appears

#17
Front (Question)

What is step 3 of Tollen’s reagent experiment (Method) (2-way)

Back (Answer)

• Add ammonia (ammonium hydroxide) • until the brown ppt disappears

#18
Front (Question)

What is step 4 of Tollen’s reagent experiment (Method) (2-way)

Back (Answer)

• Add a squirt of glucose (aldehyde substitute) • to the mixture and warm in water bath

#19
Front (Question)

What consists of Fehling’s reagent?

Back (Answer)

2 solutions

#20
Front (Question)

What is solution A of Fehling’s reagent?

Back (Answer)

Aqueous copper(II) sulfate

#21
Front (Question)

What is solution B of Fehling’s reagent?

Back (Answer)

Sodium potassium tartrate (dissolved aq sodium hydroxide don’t listen to that part it’s wrong lol)

#22
Front (Question)

What does Fehling’s reagent oxidise?

Back (Answer)

The aldehyde

#23
Front (Question)

What observations are there from aldehyde with Fehling’s reagent?

Back (Answer)

Blue to brick-red

#24
Front (Question)

What does Fehling’s reagent not oxidise?

Back (Answer)

The ketone