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Aldehydes and Ketones

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Total cards: 14•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (14)

#1
Front (Question)

The C and O double bond is…

Back (Answer)

Highly polar with a partial negative charge on the oxygen and a partial positive charge on the carbon. They are considered polar and aprotic

#2
Front (Question)

Acidity of alpha carbon

Back (Answer)

ketones have 2 aldehydes have 1 -the hydrogens are weakly acidic and can be removed -aldehydes are more acidic

#3
Front (Question)

When forming resonance, where does the negative charge want to go?

Back (Answer)

to the oxygen -when the negative charge is on the alpha carbons, it becomes more reactive

#4
Front (Question)

Boiling points

Back (Answer)

aldehydes and ketones have a lower boiling point compared to carboxylic acids and alcohols

#5
Front (Question)

The carbonyl carbon

Back (Answer)

is electrophilic with its partial positive charge

#6
Front (Question)

The alpha carbon

Back (Answer)

Functions as a nucleophile after the acidic hydrogen is removed. is negatively charged

#7
Front (Question)

Redox reactions

Back (Answer)

LEO -lose electrons -gain bonds to oxygen -lose hydrogen bonds GER -gain electrons -lose bonds to oxygen -gains hydrogen bonds

#8
Front (Question)

In order to oxidize an aldehyde…

Back (Answer)

We are going from an aldehyde to a carboxylic acid and a strong oxidizing agent is needed

#9
Front (Question)

In order to oxidize a ketone…

Back (Answer)

Cannot be oxidized into a carboxylic acid

#10
Front (Question)

In order to reduce an aldehyde or ketone…

Back (Answer)

goes to alcohol using hydride base reducing agents

#11
Front (Question)

Addition reactions

Back (Answer)

Hydration reaction

#12
Front (Question)

Hydration reaction

Back (Answer)

Water adds to carbonyl carbon via nucleophilic addition. becomes a hydroxyl group (geminal diol)

#13
Front (Question)

When treated with an alcohol

Back (Answer)

Forms hemiacetal or hemiketal

#14
Front (Question)

Cyanohydraide formation

Back (Answer)

Cyanohydrine formed