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26.1 Carbonyl Compounds

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Total cards: 13•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

What is a carbonyl compound?

Back (Answer)

any molecule containing the functional group C=O

#2
Front (Question)

What is a carbonyl group?

Back (Answer)

C=O

#3
Front (Question)

Name this molecule:

Card front image
Back (Answer)

3-methylbutan-2-one

#4
Front (Question)

Name this molecule:

Card front image
Back (Answer)

propanal

#5
Front (Question)

How are carbonyl compounds reduced?

Back (Answer)

+ NaBH4, which acts as a reducing agent by donating H atom

#6
Front (Question)

Write a general word equation for the reaction between an aldehyde + NaBH4

Back (Answer)

aldehyde + [H] ⟶ primary alcohol

#7
Front (Question)

Write a general word equation for the reaction between a ketone + NaBH4:

Back (Answer)

ketone + 2[H] ⟶ secondary alcohol

#8
Front (Question)

Why can ketones not be oxidised?

Back (Answer)

(oxidation is the loss of electrons, either by gaining oxygen or losing hydrogen) ketones cannot lose an electron in the form of a hydrogen atom, or gain oxygen

#9
Front (Question)

Under what conditions are aldehydes oxidised?

Back (Answer)

acidified potassium dichromate ions

#10
Front (Question)

Why is the gain of hydrogen considered reduction?

Back (Answer)

reduction = reduction in oxidation number due to gain of electrons H atom contains 1 electron gaining a H atom therefore means the molecule has gained 1 electron.

#11
Front (Question)

Carbonyl compound + HCN ⟶

Back (Answer)

hydroxynitrile

#12
Front (Question)

Why is HCN, hydrogen cyanide, not used in the lab during the reaction between carbonyl compounds + HCN?

Back (Answer)

HCN = highly toxic liquid boiling just above room temperature therefore sodium cyanide + sulfuric acid used instead.

#13
Front (Question)

What is the name of the reaction mechanism when aldehydes are reduced when reacting with NaBH4?

Back (Answer)

nucleophilic addition