6.3 Carboxylic Acids & Esters Flashcards

Analyse reactions and properties of carboxylic acids and derivatives. (25 cards)

1
Q

What functional group is present in carboxylic acids?

A

Carboxyl

The –COOH group contains both a carbonyl and hydroxyl group.

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2
Q

What type of compounds are formed when a carboxylic acid reacts with an alcohol?

A

Esters

The reaction is known as esterification.

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3
Q

Fill in the blank:

Carboxylic acids react with carbonates to release _______ _______ gas.

A

carbon dioxide

This reaction forms CO2, water and a salt.

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4
Q

True or False:

Carboxylic acids are strong acids in aqueous solution.

A

False

They are weak acids and only partially dissociate.

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5
Q

What catalyst is commonly used in esterification reactions?

A

Concentrated sulfuric acid

It acts as an acid catalyst and dehydrating agent.

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6
Q

True or False:

Esters often have distinctive fruity smells.

A

True

This is why they are used in perfumes and food flavourings.

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7
Q

Fill in the blank:

Esters can be hydrolysed in alkaline conditions to produce an alcohol and a _______ of a carboxylic acid.

A

salt

The salt forms because the acid reacts with the alkali.

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8
Q

What type of molecules are vegetable oils and animal fats chemically classified as?

A

Esters

They are esters formed from glycerol and fatty acids.

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9
Q

True or False:

Soap is produced by alkaline hydrolysis of fats and oils.

A

True

This process is called saponification.

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10
Q

Fill in the blank:

Hydrolysis of fats in alkaline solution produces glycerol and _______.

A

soap

Soap consists of salts of long-chain carboxylic acids.

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11
Q

What substance reacts with vegetable oils to produce biodiesel?

A

Methanol

A catalyst is used to form methyl esters.

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12
Q

What type of compounds make up biodiesel?

A

Methyl esters

These esters are derived from long-chain fatty acids.

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13
Q

What functional group is present in acyl chlorides?

A

Acyl chloride

The functional group has the structure –COCl.

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14
Q

What functional group links two acyl groups together in acid anhydrides?

A

Anhydride linkage

The structure contains –CO–O–CO–.

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15
Q

Fill in the blank:

A ** primary amide** contains the functional group _______.

A

–CONH2

Amides contain a carbonyl group attached to nitrogen.

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16
Q

True or False:

Acyl chlorides are highly reactive towards nucleophiles.

A

True

The C–Cl bond is easily attacked due to the electron-withdrawing chlorine.

17
Q

What type of reaction occurs when acyl chlorides react with nucleophiles?

A

Nucleophilic addition–elimination

The nucleophile adds to the carbonyl carbon then a leaving group is eliminated.

18
Q

True or False:

Acyl chlorides react with water to form carboxylic acids and HCl.

A

True

The reaction also produces hydrogen chloride gas.

19
Q

Fill in the blank:

Reaction of an acyl chloride with an alcohol produces an _______.

A

ester and HCl

The alcohol replaces the chlorine atom.

20
Q

What product forms when an acyl chloride reacts with ammonia?

A

Amide

Ammonia acts as a nucleophile and replaces the chloride. This reaction also produces HCl gas

21
Q

True or False:

Primary amines reacting with acyl chlorides produce ** N-substituted amides**.

A

True

The –NH2 group acts as the nucleophile.

22
Q

Fill in the blank:

In nucleophilic addition–elimination reactions, the nucleophile first attacks the _______ carbon.

A

carbonyl

This forms a tetrahedral intermediate.

23
Q

Why is ethanoic anhydride often preferred to ethanoyl chloride in aspirin manufacture?

A

Safer and less corrosive as it doesn’t produce toxic HCl gas

It produces fewer hazardous by-products.

24
Q

What type of molecule acts as the nucleophile in acylation reactions?

A

Electron pair donor

Examples include water, alcohols and amines.

25
Give 4 common uses of esters
solvents plasticisers perfumes food flavourings ## Footnote They are good polar solvents due to their polar nature. They are good plasticisers as they can slide in between polymer chains. They are good perfumes and food flavourings due to their sweer smell.