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26.4 Carboxylic Acid Derivatives

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

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#1
Front (Question)

What are carboxylic acid derivatives?

Back (Answer)

molecules which can be HYDROLYSED to form CARBOXYLIC ACIDS

#2
Front (Question)

What are 4 examples of carboxylic acid derivatives?

Back (Answer)

ESTERS ACYL CHLORIDES AMIDES ACID ANHYDRIDES

#3
Front (Question)

What group do all carboxylic acid derivatives contain?

Back (Answer)

acyl group RCO (OH from carboxylic acid is removed + replaced)

#4
Front (Question)

What is the functional group of esters?

Back (Answer)

-COOR

#5
Front (Question)

What is the functional group of acyl chlorides?

Back (Answer)

-COCl

#6
Front (Question)

What is esterification?

Back (Answer)

Reaction of CARBOXYLIC ACID + ALCOHOL ⟶ ESTER + WATER

#7
Front (Question)

Under what 2 conditions can esters be hydrolysed in?

Back (Answer)

ACIDIC hydrolysis ALKALINE hydrolysis

#8
Front (Question)

What does acidic hydrolysis of an ester form?

Back (Answer)

CARBOXYLIC ACID + ALCOHOL (reverse of esterification)

#9
Front (Question)

What does alkaline hydrolysis of an ester form?

Back (Answer)

CARBOXYLATE + ALCOHOL (reflux with aqueous OH-)

#10
Front (Question)

During general hydrolysis of an ester, what condition is used to make sure the reaction is complete?

Back (Answer)

reflux

#11
Front (Question)

What do you call molecules which can be HYDROLYSED to form carboxylic acids?

Back (Answer)

carboxylic acid derivatives

#12
Front (Question)

How do you form a carboxylic acid from a carboxylate?

Back (Answer)

Add H+ ions

#13
Front (Question)

How do you prepare an ester in the lab?

Back (Answer)

• alcohol + carboxylic acid (1:1) • • Concentrated H2SO4 catalyst • Place in water bath @ 80°C - ester has formed, but unreacted carboxylic acid remains. • • aqueous sodium carbonate which reacts with excess carboxylic acid to remove, forming salt + water + carbon dioxide.

#14
Front (Question)

What is alkaline hydrolysis also known as?

Back (Answer)

saponification

#15
Front (Question)

Which hydrolysis is irreversible?

Back (Answer)

saponification / alkaline hydrolysis

#16
Front (Question)

What are the reactions of acyl chlorides?

Back (Answer)

+ ALCOHOL ⟶ ESTER + PHENOL ⟶ ESTER + WATER ⟶ CARBOXYLIC ACID + AMMONIA/AMINE ⟶ AMIDE

#17
Front (Question)

How are acyl chlorides prepared?

Back (Answer)

Carboxylic acid + SOCl2 ⟶ ACYL CHLORIDE + SO2(g) + HCl(g)

#18
Front (Question)

What products made when WATER added to acyl chloride?

Back (Answer)

carboxylic acid + HCl GAS

#19
Front (Question)

What products made when ALCOHOL added to acyl chloride?

Back (Answer)

ester + HCl

#20
Front (Question)

What products made when PHENOL added to acyl chloride?

Back (Answer)

ester + HCl

#21
Front (Question)

What are the conditions for esterification?

Back (Answer)

Concentrated sulfuric acid

#22
Front (Question)

What are the conditions for acid hydrolysis?

Back (Answer)

reflux + dilute acid catalyst

#23
Front (Question)

Which bond is broken in an ester during hydrolysis?

Back (Answer)

C–O

#24
Front (Question)

What are the conditions for alkaline hydrolysis?

Back (Answer)

aqueous OH- reflux