Carboxylic Acids | Ester | Carboxylic Acid


What are carboxylic acids?
‡ Carboxylic acids are compounds which contain a -COOH group.

Salts of carboxylic acids
‡ Carboxylic acids are acidic because of the hydrogen in the -COOH group. ‡ When the acids form salts, this is lost and replaced by a metal. Sodium ethanoate, for example, has the structure:

boiling point and solubility) of the carboxylic acids are governed by their ability to form hydrogen bonds.Physical properties of carboxylic acids ‡ The physical properties (for example. .

hydrogen bonding can occur between two molecules of acid to produce a dimer.2°C 118°C ‡The boiling points of carboxylic acids of similar size are higher still. . ‡The higher boiling points of the carboxylic acids are still caused by hydrogen bonding. but operating in a different way. ‡In a pure carboxylic acid.Boiling points propan-1-ol ethanoic acid CH3CH2CH2OH CH3COOH 97.

resulting in a high boiling point.‡ This immediately doubles the size of the molecule and so increases the van der Waals dispersion forces between one of these dimers and its neighbours . .

‡ This is because the longer hydrocarbon "tails" of the molecules get between water molecules and break hydrogen bonds. In this case. ‡ Instead. ‡ The solubility of the bigger acids decreases very rapidly with size. ‡ The carboxylic acids with up to four carbon atoms will mix with water in any proportion. the carboxylic acids don't dimerise. hydrogen bonds are formed between water molecules and individual molecules of acid.Solubility in water ‡ In the presence of water. . these broken hydrogen bonds are only replaced by much weaker van der Waals dispersion forces.

by oxidising primary alcohols or aldehydes ‡ Primary alcohols are oxidised to carboxylic acids in two stages .1. MAKING CARBOXYLIC ACIDS .first to an aldehyde and then to the acid .

you could combine these into one single equation to give: ‡ Eg : .‡ Starting from the primary alcohol.

2. Making carboxylic acids by hydrolysing nitriles ‡ What are nitriles? ‡ Nitriles are compounds which contain -CN attached to a hydrocarbon group. ‡ Some common examples include: .

.Converting the nitrile into a carboxylic acid ‡ There are two ways of doing this. both of which involve reacting the carbon-nitrogen triple bond with water. ‡ This is described as hydrolysis of nitriles ‡ The two methods produce slightly different products .you just have to be careful to get this right.

Acid hydrolysis ‡ The nitrile is heated under reflux with a dilute acid such as dilute hydrochloric acid. starting from ethanenitrile you would get ethanoic acid. The ethanoic acid could be distilled off the mixture. ‡ For example. . A carboxylic acid is formed.

‡ To liberate the weak acid. ethanoic acid. you just have to supply hydrogen ions from a strong acid such as hydrochloric acid. .Alkaline hydrolysis ‡ The nitrile is heated under reflux with an alkali such as sodium hydroxide solution.

‡ In solution in water. a hydrogen ion is transferred from the -COOH group to a water molecule.The acidity of the carboxylic acids ‡ The carboxylic acids are acidic because of the hydrogen in the -COOH group. . ‡ For example.

‡ No more than about 1% of the acid has reacted to form ions at any one time. ‡ These are therefore weak acids. ‡ RCOOH + H2O Relatively less stable RCOO.+ H30+ relatively more stable .

depending on their concentrations.The pH of carboxylic acid solutions ‡ The pH depends on both the concentration of the acid and how easily it loses hydrogen ions from the -COOH group.3 range. ‡ Typical lab solutions have pH's in the 2 . ‡ Ethanoic acid is typical of the acids where the -COOH group is attached to a simple alkyl group. .

With metals ‡ Carboxylic acids react with the more reactive metals to produce a salt and hydrogen. .Reactions of the carboxylic acids 1.

2. . With metal hydroxides ‡ These are simple neutralisation reactions and are just the same as any other reaction in which hydrogen ions from an acid react with hydroxide ions.

‡ For carbonates: ‡ For hydrogencarbonates: .3. a salt is formed together with carbon dioxide and water. With carbonates and hydrogencarbonates ‡ In both of these cases.

‡ The full equation is: .

. With ammonia colourless solution of ammonium ethanoate.4.

5. With amines ‡ Amines are compounds in which one or more of the hydrogen atoms in an ammonia molecule have been replaced by a hydrocarbon group such as an alkyl group. ‡ Simple primary amines include : .

For example. ‡ ethanoic acid reacts with methylamine to produce a colourless solution of the salt methylammonium ethanoate. .

ethyl ethanoate .ESTERIFICATION OF CARBOXYLIC ACIDS ‡ What are esters? ‡ Esters have a hydrocarbon group of some sort replacing the hydrogen in the -COOH group of a carboxylic acid. ‡ A common ester .

A few more esters .

Making esters ‡ Esters are produced when carboxylic acids are heated with alcohols in the presence of an acid catalyst. ‡ The catalyst is usually concentrated sulphuric acid. .

flavourings and preservatives ‡ Excellent solvents for many organic compounds (drugs. antibiotics. etc) ‡ Production of polyesters .Uses of esters ‡ Used as taste enhancers.

(lithium aluminium hydride). LiAlH4 .REDUCTION OF CARBOXYLIC ACIDS The reducing agent ‡ Lithium tetrahydridoaluminate(III).

.‡ The reaction happens in two stages .first to form an aldehyde and then a primary alcohol.

CONVERTING CARBOXYLIC ACIDS INTO ACYL CHLORIDES (ACID CHLORIDES) nucleophilic substitution reaction ‡ Replacing -OH by -Cl .

‡ It leaves a liquid mixture of the acyl chloride and a phosphorus compound.1.POCl3. . Replacing the -OH group using phosphorus(V) chloride. phosphorus trichloride oxide (phosphorus oxychloride) . PCl5 ‡ Phosphorus(V) chloride is a solid which reacts with carboxylic acids in the cold to give steamy acidic fumes of hydrogen chloride.

Replacing the -OH group using phosphorus(III) chloride. . ‡ Its reaction with a carboxylic acid is less dramatic than that of phosphorus(V) chloride because there is no hydrogen chloride produced. PCl3 ‡ Phosphorus(III) chloride is a liquid at room temperature.2.

3. Replacing the -OH group using sulphur dichloride oxide (thionyl chloride) ‡ Sulphur dichloride oxide (thionyl chloride) is a liquid at room temperature and has the formula SOCl2. .

THE DECARBOXYLATION OF CARBOXYLIC ACIDS AND THEIR SALTS ‡ In decarboxylation. the -COOH or -COONa group is removed and replaced with a hydrogen atom. .

‡ The solid sodium salt of a carboxylic acid is mixed with solid soda lime. . benzene can be made by heating soda lime with solid benzoic acid (benzenecarboxylic acid). ‡ For example. and the mixture is heated. C6H5COOH.

polyvinyl acetate plastic (PVA) .Uses of Carboxylic Acids in Industry ‡ Methanoic acid and ethanoic acid are used to coagulate rubber latex ‡ Methanoic acid is also used in textile dyeing and in leather tanning ‡ Ethanoic acid is use in the food industry as vinegar. It is used in the manufacturing industry to produce vinyl acetate (CH3COOCH=CH2) ‡ Vinyl acetate is polymerised to form polymer.

Uses of Carboxylic Acids in Industry ‡ Manufacture of nylon ‡ Preservatives in foodstuffs ‡ Preparation of medicines .

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