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Chapter 26: Carboxylic Acids and Esters

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

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#1
Front (Question)

What functional group do carboxylic acids have, and what does this contain?

Back (Answer)

• Carboxyl groups • They contain both a carbonyl and hydroxyl group bonded to the same carbon atom, which is what makes them react differently

#2
Front (Question)

Are carboxylic acids soluble? Explain why.

Back (Answer)

• The C=O and O-H bonds are polar, which allows carboxylic acids to form hydrogen bonds with the water molecules and dissolve in water • However, once there are more than 4 carbon atoms in a carboxylic acid molecules, they are no longer soluble, as the non-polar carbon chain has a greater effect

#3
Front (Question)

What type of carboxylic acids are more soluble than the others, and why?

Back (Answer)

• Dicarboxylic acids • They have 2 polar carboxyl groups to form hydrogen bonds

#4
Front (Question)

What happens when carboxylic acids dissolve in water? What does this mean?

Back (Answer)

• They partially dissociate • They are weak acids

#5
Front (Question)

Give the equation for the dissociation of methanoic acid, including state symbols.

Back (Answer)

• HCOOH (aq) <-> H+ (aq) + HCOO- (aq)

#6
Front (Question)

Which reactions do carboxylic acids have in common with other acids?

Back (Answer)

• Redox reactions with metals • Neutralisation reactions with bases (alkalis, metal oxides and carbonates)

#7
Front (Question)

What observations can be made during the reaction of carboxylic acids with metals?

Back (Answer)

• The metal dissolves • Effervescence

#8
Front (Question)

What observations can be made during the reaction of carboxylic acids with carbonates?

Back (Answer)

• The carbonate dissolves if the carboxylic acid is in excess • Effervescence

#9
Front (Question)

How can carboxylic acids be told apart from other organic compounds? Why does this method work?

Back (Answer)

• They are reacted with carbonates • They are the only common organic compound that is acidic enough to react with carbonates

#10
Front (Question)

What are carboxylic acid derivatives?

Back (Answer)

• Compounds that are formed (derived) from carboxylic acids

#11
Front (Question)

List 4 derivatives of carboxylic acids, and the functional group of each.

Back (Answer)

• Esters, RCOOR (second R cannot be a hydrogen atom) • Acyl chlorides, RCOCl • Acid anhydrides, RCOOCOR/ (RCO)2O • Amides, RCONR2

#12
Front (Question)

What causes carboxylic acid derivatives to react in similar ways?

Back (Answer)

• They all have an acyl group (RC=O, called that and not a carbonyl group since it comes from a carboxylic acid) bonded to an electronegative atom

#13
Front (Question)

How are esters formed? What is this reaction called?

Back (Answer)

• Alcohol + carboxylic acid -> ester + water • Conditions: heat, sulfuric acid catalyst • Esterification

#14
Front (Question)

How are simple esters named?

Back (Answer)

• The alcohol’s name changes to end in -yl (e.g. methyl) • The name of the carboxylic acid changes to end in -oate (e.g. propanoate) • (E.g. methyl propanoate) • However, if the OH group is on the second carbon, for example, the ester would be called 2-propyl methanoate

#15
Front (Question)

How are esters with substituents named?

Back (Answer)

• The carbon atoms in the ester bond are both numbered 1 in their part of the chain

#16
Front (Question)

What is hydrolysis?

Back (Answer)

• A reaction with water (or in the presence of an aqueous solution) that breaks a chemical compound into 2 compounds

#17
Front (Question)

What can esters be hydrolysed by?

Back (Answer)

• Aqueous acid • Aqueous alkali

#18
Front (Question)

Give the general equation and conditions for the hydrolysis of esters by aqueous acid.

Back (Answer)

• Ester + water -> carboxylic acid + alcohol • Conditions: reflux, aqueous H2SO4

#19
Front (Question)

Give the general equation and conditions for the hydrolysis of esters by aqueous alkali.

Back (Answer)

• Ester + hydroxide ion -> carboxylate ion + alcohol • Conditions: reflux, aqueous NaOH

#20
Front (Question)

What are 3 differences between the hydrolysis of esters by aqueous acid and aqueous alkali?

Back (Answer)

• The hydrolysis of esters by aqueous acid is reversible, but with aqueous alkali, it’s irreversible • The acid is a catalyst, but the alkali is used up • In the reversible reaction, some ester will remain in the mixture, but in the irreversible reaction, provided that there is enough NaOH, the ester will be completely converted

#21
Front (Question)

Other than carboxylic acids, what else can produce esters?

Back (Answer)

• Acid anhydrides • Acyl chlorides

#22
Front (Question)

What can phenols be esterified by, and why?

Back (Answer)

• Only acid anhydrides and acyl chlorides • Carboxylic acids are not reactive enough to esterify them

#23
Front (Question)

How are acid anhydrides named?

Back (Answer)

• If it is formed from 2 of the same carboxylic acid, the word acid is replaced with anhydride • For example, 2 ethanoic acid molecules would form ethanoic anhydride • If 2 different carboxylic acids are used, put their names in alphabetical order (e.g. butanoic propanoic anhydride)

#24
Front (Question)

How do acid anhydrides react to form esters? Give a general equation.

Back (Answer)

• Acid anhydride + alcohol -> ester + carboxylic acid