Carboxylic Acids and their Derivatives

Carboxylic Acids and their Derivatives
Chapter 35 Carboxylic Acids and their Derivatives 35.1 Introduction 35.2 Nomenclature of Carboxylic Acids and their Derivatives 35.3 Physical Properties of Carboxylic Acids 35.4 Preparation of Carboxylic Acids 35.5 Reactions of Carboxylic Acids 35.6 Reactions of the Derivatives of Carboxylic Acids 35.7 Uses of Carboxylic Acids and their Derivatives

Carboxylic acids refer to the class of organic compounds
35.1 Introduction (SB p.29) Carboxylic acids refer to the class of organic compounds with the carboxyl group

General formula of carboxylic acid: RCOOH Examples:
35.1 Introduction (SB p.29) General formula of carboxylic acid: RCOOH Examples:

Name Structure Acyl chlorides Acid anhydrides Amides Esters
35.1 Introduction (SB p.30) Carboxylic acid derivatives Name Structure Acyl chlorides Acid anhydrides Amides Esters

35.2 Nomenclature of Carboxylic Acids and their Derivatives (SB p.30)
Carboxylic acids are named by replacing the final “-e” of the name of the corresponding alkane with “-oic acid” When other substituents are present, the carboxyl carbon is assigned position 1 Examples:

Acyl Chlorides Acyl chlorides are named by replacing the final “-ic acid” of the name of the parent carboxylic acid with “-yl chloride” Examples:

Acid Anhydrides Acid anhydrides are named by dropping the word “acid” from the name of the parent carboxylic acid and then adding the word “anhydride” Examples:

Amides Amides that have no substituents on the nitrogen atom are named by replacing “-oic acid” from the parent carboxylic acid with “amide” Substituents on the nitrogen atom of amides are named and the named substituent is preceded by N-, or N,N- Examples:

The portion of the name derived from the alcohol comes first Examples:
35.2 Nomenclature of Carboxylic Acids and their Derivatives (SB p.31) Esters The names of esters are derived from the names of the alcohol (with the ending “-yl”) and the carboxylic acid (with the ending “-oate”) The portion of the name derived from the alcohol comes first Examples:

Example 35-1 Give the IUPAC names of the following compounds: (a) (b)
35.2 Nomenclature of Carboxylic Acids and their Derivatives (SB p.32) Example 35-1 Give the IUPAC names of the following compounds: (a) (b) (c) (d) Solution: (a) 3-Methylbutanoic acid (b) N-methylethanamide (c) Ethyl benzoate (d) Benzoic anhydride Answer

Example 35-2 An ester is formed by reacting an alcohol with a carboxylic acid. Draw the structural formula of the following ester molecule and give the name of the alcohol and the carboxylic acid that form the ester. (a) Methyl ethanoate Answer Solution: (a) The structural formula of methyl ethanoate is: It is formed from the reaction of ethanoic acid and methanol.

Example 35-2 An ester is formed by reacting an alcohol with a carboxylic acid. Draw the structural formula of the following ester molecule and give the name of the alcohol and the carboxylic acid that form the ester. (b) Ethyl methanoate Answer Solution: (b) The structural formula of ethyl methanoate is: It is formed from the reaction of methanoic acid and ethanol.

Check Point 35-1 Complete the following table by filling in the molecular formulae, structural formulae or IUPAC names of the carboxylic acids. (a) (b) Butanoic acid (c) CH3CH(CH3)CH2COOH (d) 3-Methylbutanoic acid (e) C6H4ClCOOH (f) 2-Chlorobenzoic acid (g) CCl3COOH (h) Molecular formula Structural formula IUPAC name C3H7COOH (a) (b) (c) (d) (e) (f) (g) (h) Trichloroethanoic acid Answer

Carboxylic acids are colourless liquids at room conditions
35.3 Physical Properties of Carboxylic Acids (SB p.34) Carboxylic acids are colourless liquids at room conditions They have characteristic pungent smell and sour taste Carboxylic acid Formula Boiling point (°C) Melting point (°C) Density at 20°C (g cm–3) Methanoic acid Ethanoic acid Propanoic acid Butanoic acid Pentanoic acid Hexanoic acid Benzoic acid Phenylethanoic acid 2-Methylpropanoic acid Chloroethanoic acid HCO2H CH3CO2H CH3CH2CO2H CH3(CH2)2CO2H CH3 (CH2)3CO2H CH3 (CH2)4CO2H C6H5CO2H C6H5CH2CO2H (CH3)2CHCO2H CH2ClCO2H 101 118 141 164 186 205 249 266 154 189 8.4 16.6 –20.8 –6.5 –34.5 –1.5 122 76 –47 63 1.220 1.049 0.992 0.964 0.939 0.927 — 0.950

35.3 Physical Properties of Carboxylic Acids (SB p.34)
Formula Boiling point (°C) Melting point (°C) Density at 20°C (g cm–3) Dichloroethanoic acid Trichloroethanoic acid Hydroxyethanoic acid 2-Hydroxypropanoic acid Cis-Butenedioic acid Trans-Butenedioic acid Ethanedioic acid Propandioic acid Butanedioic acid Benzene-1,2-dicarboxylic acid CHCl2CO2H CCl3CO2H HOCH2CO2H CH3CHOHCO2H HO2CCH = CHCO2H HO2CCO2H HO2CCH2CO2H HO2C(CH2)2CO2H C6H4(CO2H)2 194 198 dec. — 235 (dec.) 10.8 57.7 79 16.8 130 – 131 268 (dec.) 190 (dec.) 136 (dec.) 182 206 (dec.) 1.566 1.249 1.590 1.635

Boiling Point and Melting Point
35.3 Physical Properties of Carboxylic Acids (SB p.35) Boiling Point and Melting Point Due to formation of intermolecular hydrogen bonds  high b.p. and m.p. The hydrogen bonds are more extensive than those in alcohols  higher b.p. and m.p. than alcohols

Density The densities of carboxylic acids decrease with increasing relative molecular masses Only methanoic acid and ethanoic acid are denser than water at 20°C ∵ closer packing of the smaller molecules in the liquid phase

First four carboxylic acids are miscible with water
35.3 Physical Properties of Carboxylic Acids (SB p.36) Solubility Carboxylic acids of low molecular masses show appreciable solubilities in water ∵ carboxylic acids are polar and can form strong hydrogen bonds with water molecules First four carboxylic acids are miscible with water The length of the hydrocarbon portion   solubilities in water 

Example 35-3 (a) Propanoic acid has a boiling point of 141°C which is considerably higher than that of butan-1-ol (117°C), although they have the same molecular mass. Explain why. Answer Solution: (a) Each propanoic acid molecule forms two intermolecular hydrogen bonds with another propanoic acid molecule. However, two butan-1-ol molecules form only one hydrogen bond. As molecules of propanoic acid form more extensive intermolecular hydrogen bonds than those of butan-1-ol, the boiling point of propanoic acid is higher than that of butan-1-ol.

Example 35-3 (b) Rank the following compounds in decreasing order of solubility in water: CH3CH2CH2COOH, CH3CH2COOCH3, CH3COOH Answer Solution: (b) The solubility of the compounds in water decreases in the order: CH3COOH > CH3CH2CH2COOH > CH3CH2COOCH3

Example 35-3 (c) Propanedioic acid forms intramolecular hydrogen bonds. Draw its structural formula showing clearly the formation of intramolecular hydrogen bonds. Answer Solution: (c)

Hydrolysis of Nitriles
35.4 Preparation of Carboxylic Acids (SB p.37) Hydrolysis of Nitriles 2-hydroxyalkanenitriles is formed by nucleophilic addition reaction of aldehydes or ketones with hydrogen cyanide Acid hydrolysis or alkaline hydrolysis of 2-hydroxyalkanenitriles produce carboxylic acids or carboxylate ions respectively

35.4 Preparation of Carboxylic Acids (SB p.37)
Nitriles can be formed by nucleophilic substitution reaction of haloalkanes with sodium cyanide Acid hydrolysis of the nitrile produces a carboxylic acid with one more carbon atom e.g.

Reactive derivatives react vigorously with water, e.g. acyl chlorides
35.4 Preparation of Carboxylic Acids (SB p.38) Hydrolysis of Esters Hydrolysis of esters give parent carboxylic acids and alcohols by boiling under reflux with the dilute HCl or dilute H2SO4 Acyl chlorides, acid anhydrides, esters and amides can be hydrolyzed to give the corresponding carboxylic acids Reactive derivatives react vigorously with water, e.g. acyl chlorides Less reactive derivatives require more severe conditions to bring about the reaction

Oxidation of Alcohols and Aldehydes
35.4 Preparation of Carboxylic Acids (SB p.38) Oxidation of Alcohols and Aldehydes Aldehydes and 1° alcohols can be oxidized to carboxylic acids by KMnO4/H+

Examples:

Oxidation of Alkybenzenes
35.4 Preparation of Carboxylic Acids (SB p.39) Oxidation of Alkybenzenes 1° and 2° alkyl groups (but not 3°) directly attached to a benzene ring are oxidized by hot KMnO4/OH– to carboxyl group e.g. This oxidation takes place initially at the benzylic carbon  alkyl groups longer than methyl group are ultimately degraded to benzoic acid

Check Point 35-2 Write the equations for the acid-catalyzed and base-catalyzed hydrolyses of each of the following substances: (a) Ethyl butanoate (a) Answer

Check Point 35-2 Write the equations for the acid-catalyzed and base-catalyzed hydrolyses of each of the following substances: (b) Propanamide (b) Answer

Check Point 35-2 Write the equations for the acid-catalyzed and base-catalyzed hydrolyses of each of the following substances: (c) Benzoyl chloride (c) Answer

Acidity of Carboxylic Acids
35.5 Reactions of Carboxylic Acids (SB p.39) Acidity of Carboxylic Acids Carboxylic acids are weak acids Their acidic properties are due to the presence of ionizable hydrogen atom

35.5 Reactions of Carboxylic Acids (SB p.39)
e.g. ethanoic acid The acid strength of ethanoic acid is shown by the value of its acid dissociation constant (Ka) pKa is used for convenience as Ka is small for weak acids pKa = –log Ka , the smaller the pKa value, the stronger is the acid

Unsubstituted carboxylic acids have pKa values in the range of 3 to 5
35.5 Reactions of Carboxylic Acids (SB p.40) Unsubstituted carboxylic acids have pKa values in the range of 3 to 5 Alcohols have pKa values in 15 to 18  carboxylic acids are much more acidic than alcohols Name Formula pKa Methanoic acid Ethanoic acid Propanoic acid Butanoic acid Benzoic acid HCOOH CH3COOH CH3CH2COOH CH3CH2CH2COOH C6H5COOH 3.75 4.76 4.87 4.82 4.20

Resonance Effect The greater stability of carboxylic acids is attributed to resonance stabilization of the carboxylate ions Example:

No stabilizing resonance structures for alkoxide ions e.g.
35.5 Reactions of Carboxylic Acids (SB p.41) By the resonance effect, the ethanoate ion can be stabilized by spreading the negative charge over two oxygen atoms No stabilizing resonance structures for alkoxide ions e.g. Carboxylic acids are much acidic than alcohols ∵ formation of more stable conjugate base

Inductive Effect Both compounds contain the highly polarized O – H bond due to the difference in electronegativity The greater acidity of ethanoic acid is due to the presence of the powerful electron-withdrawing carbonyl group

Two resonance structures for the carbonyl group:
35.5 Reactions of Carboxylic Acids (SB p.41) Two resonance structures for the carbonyl group: The carbonyl atom of ethanoic acid bears a large partial positive charge and exerts a powerful electron- withdrawing inductive effect to hydroxyl oxygen atom, making the hydroxyl hydrogen atom much more positive  proton dissociate more readily The electron-withdrawing inductive effect of the carbonyl group stabilizes the carboxylate ion  carboxylic acids are stronger acid than alcohols

Inductive Effects of Other Groups
35.5 Reactions of Carboxylic Acids (SB p.42) Inductive Effects of Other Groups 1. Electron-withdrawing Groups The presence of electron-withdrawing groups increase the acidity of a carboxylic acid e.g.

The chlorine atom withdraws electron from the carbonyl group and oxygen making the hydroxyl hydrogen more positive than that of ethanoic acid The chlorine atom also stabilizes the chloroethanoate ion to greater extent

Effect of electron-withdrawing substituents on the acidity of carboxylic acids Acidity pKa CH3COOH < < < CCl3COOH Ethanoic Chloroethanoic Dichloroethanoic Trichloroethanoic acid acid acid acid Acidity pKa CH3COOH < < < < Ethanoic Iodoethanoic Bromoethanoic Chloroethanoic Fluoroethanoic acid acid acid acid acid The greater the number of electron-withdrawing groups, the stronger is the acid The more electronegative of halogen substituents (F > Cl > Br > I), the stronger is the acid

The further away of the substituents from the carboxyl group, the weaker is the acid < < 4-Chlorobutanoic 3-Chlorobutanoic 2-Chlorobutanoic acid acid acid Acidity pKa

2. Electron-releasing Groups
35.5 Reactions of Carboxylic Acids (SB p.43) 2. Electron-releasing Groups The presence of electron-releasing groups reduce the acidity of a carboxylic acid e.g.

Electron-releasing alkyl groups release electrons towards the electron-deficient carbonyl carbon, thus reducing its charge Reduce the positive character of the hydroxyl hydrogen atom  dissociate less readily Intensify the negative charge on the carboxyl group  destablizes the ethanoate ion

Check Point 35-3 (a) Match the Ka values: 2.19  10–3 M and 1.26  10–3 M, to the carboxylic acids: CH2FCOOH and CH2BrCOOH. Explain your answer briefly. (a) The greater the Ka value, the stronger is the acid. CH2FCOOH is a stronger acid than CH2BrCOOH. This –F substituent exerts a stronger inductive effect than the –Br substituent, as fluorine is more electronegative than bromine. The –F substituent stabilizes the conjugate base (i.e. CH2FCOOH–) to a greater extent than the –Br substituent. Therefore, CH2FCOOH has a Ka value of 2.19  10–3 M, and CH2BrCOOH has a Ka value of 1.26  10–3 M. Answer

Check Point 35-3 (b) Arrange the following acids in ascending order of acidity: CHCl2COOH, CCl3COOH, CH2ClCOOH, CH3COOH Explain the order briefly. (b) CH3COOH < CH2ClCOOH < CHCl2COOH < CCl3COOH The –Cl substituent is an electron-withdrawing group. An increasing number of the –Cl substituent brings about a greater negative inductive effect. Thus, the conjugate base will be stabilized more, and the acidity of the acid increases. Answer

Check Point 35-3 (c) Arrange the following aryl carboxylic acids in descending order of acidity: Explain the order briefly.

is more acidic than ,because contains the –Cl substituent which is an electron-withdrawing group. Thus, it exerts a negative inductive effect to the conjugate base, and hence stabilizes the carboxylate ion formed. is less acidic than , because contains a methyl group which is an electron-releasing group. Thus, it exerts a positive inductive effect to the conjugate base, and hence destabilizes the carboxylate ion formed.

Check Point 35-3 (d) Which is a stronger acid, CH2ClCOOH or CH3CHClCOOH? Explain your answer briefly. Answer (d) CH2ClCOOH is a stronger acid as CH3CHClCOOH contains a methyl group which is an electron-releasing group. It exhibits a positive inductive effect and thus destabilizes the conjugate base of the acid. Therefore, CH3CHClCOOH is less acidic.

Reaction with Active Metals
35.5 Reactions of Carboxylic Acids (SB p.44) Formation of Salts Reaction with Active Metals Carboxylic acids react with reactive metals such as Na or Mg to give the corresponding metal carboxylates and hydrogen gas

Example:

Reaction with Bases Carboxylic acids react with strong alkalis such as NaOH to form sodium carboxylates and water Examples:

Carboxylic acids also react weak alkalis such as Na2CO3 or NaHCO3 to form sodium carboxylates, carbon dioxide and water

Examples: This reaction serves as a test to distinguish carboxylic acids and other acidic organic compounds

NaOH and Na2CO3 can be used to separate a mixture of alcohols, phenols and carboxylic acids

Check Point 35-4 (a) Describe how to separate a mixture of benzoic acid and phenol in the laboratory. Answer (a) Sodium hydrogencarbonate, water and diethyl ether are added to the mixture. Benzoic acid reacts with sodium hydrogencarbonate to form a water-soluble salt which dissolves in the aqueous layer. After separation by the use of a separating funnel, phenol can be recovered by distilling off the ether. To the aqueous layer, hydrochloric acid is added to generate the benzoic acid which can be extracted by diethyl ether. After separation from the aqueous layer, benzoic acid is obtained by distilling off the ether.

Check Point 35-4 (b) Outline how a mixture of butanone and ethanoic acid can be separated in the laboratory. Answer

Formation of Acyl Chlorides
35.5 Reactions of Carboxylic Acids (SB p.47) Formation of Acyl Chlorides Acyl chlorides are the most reactive amongst the carboxylic acid derivatives They can be prepared by the use of SOCl2, PCl3 or PCl5 in good yields

Acyl chlorides can be used to prepare aldehydes, ketones, esters, amides and acid anhydrides in organic synthesis Acyl chlorides are extremely sensitive to moisture, therefore, it must be stored in anhydrous conditions ∵ hydrolyze rapidly to form carboxylic acids

Formation of Acid Anhydrides
35.5 Reactions of Carboxylic Acids (SB p.47) Formation of Acid Anhydrides Acid anhydrides can be prepared by reacting acyl chlorides with carboxylic acids in the presence of pyridine This can be used to prepare mixed anhydrides (R  R´) or simple anhydrides (R = R´)

Acyl chlorides react with sodium salts of carboxylic acids to give acid anhydrides

Formation of Amides Ammonia reacts with carboxylic acids to form ammonium salts. The dry salts are heated to dehydrate to give amide The better way to prepare amides is reacting ammonia or amines with acyl chlorides

Esterification reactions are acid-catalyzed and reversible
35.5 Reactions of Carboxylic Acids (SB p.48) Formation of Esters Carboxylic acids react with alcohols to form esters through condensation reactions Esterification reactions are acid-catalyzed and reversible

Reduction with Lithium Tetrahydridoaluminate
35.5 Reactions of Carboxylic Acids (SB p.48) Reduction with Lithium Tetrahydridoaluminate LiAlH4 is a powerful reducing agent which reduces carboxylic acids to primary alcohols in good yields Example:

Example 35-4 (a) Complete and balance the following acid-base equations: (i) (ii) Solution: (a) (i) (ii) Answer

Example 35-4 (b) Draw the structural formulae for the products formed from the following compounds when they are reduced with lithium tetrahydridoaluminate. (i) (ii) Solution: (b) (i) (ii) HOCH2CH2CH2CH2OH Answer

Example 35-4 (c) Complete the following equations: Solution: (i) (ii)
35.5 Reactions of Carboxylic Acids (SB p.49) Example 35-4 (c) Complete the following equations: (i) (ii) (iii) Solution: (c) (i) (ii) (iii) Answer

Reactions of Acyl Chlorides
35.6 Reactions of the Derivatives of Carboxylic Acids (SB p.50) Reactions of Acyl Chlorides Both chlorine and oxygen atoms are electron- withdrawing groups, thus making the acyl carbon much electron-deficient  acyl carbon is a good nucleophilic site Chloride ion is a good leaving group which is substituted by other atoms or groups easily  acyl chlorides are very reactive

35.6 Reactions of the Derivatives of Carboxylic Acids (SB p.50)
Benzoyl chloride is much less reactive than aliphatic acyl chlorides ∵ reduction of electron-deficiency on the acyl carbon due to delocalization of electrons (resonance effect)

Reaction with Water Acyl chlorides are hydrolyzed by water to form the parent carboxylic acids and hydrogen chloride Examples:

Reaction with Alcohols
35.6 Reactions of the Derivatives of Carboxylic Acids (SB p.51) Reaction with Alcohols Acyl chlorides react with alcohols to give esters and HCl Examples:

Acyl chlorides react with phenols to give esters in the presence of base as catalyst ∵ an alkaline medium converts phenol to a powerful nucleophile, phenoxide ion Example:

Reaction with Ammonia and Amines
35.6 Reactions of the Derivatives of Carboxylic Acids (SB p.52) Reaction with Ammonia and Amines Acyl chlorides react with ammonia to form amides rapidly Example:

This method is widely used in laboratory for amides synthesis
35.6 Reactions of the Derivatives of Carboxylic Acids (SB p.52) Acyl chlorides react rapidly with 1° and 2° amines to form N-, N,N- substituted amides respectively The reaction takes place at room temperature and produces amides in high yield This method is widely used in laboratory for amides synthesis

Check Point 35-5 Explain why ethanoyl chloride must be protected from atmospheric moisture during storage. Answer This is because ethanoyl chloride reacts readily with water (from atmospheric moisture) to form ethanoic acid.

Reactions of Acid Anhydrides
35.6 Reactions of the Derivatives of Carboxylic Acids (SB p.53) Reactions of Acid Anhydrides Reaction with Water Acid anhydrides undergo hydrolysis to form carboxylic acids Example:

Reaction with Alcohols
35.6 Reactions of the Derivatives of Carboxylic Acids (SB p.53) Reaction with Alcohols Acid anhydrides react with alcohols to form esters in the presence of acid catalyst Example:

Reaction with Ammonia and Amines
35.6 Reactions of the Derivatives of Carboxylic Acids (SB p.54) Reaction with Ammonia and Amines Acid anhydrides react with ammonia and with 1° and 2° amines in the ways similar to those of acyl chlorides

Examples:

∵ NH2–, NHR– or NR2– are strong bases and thus poor leaving groups
35.6 Reactions of the Derivatives of Carboxylic Acids (SB p.53) Reactions of Amides Amides are the least reactive among the carboxylic acid derivatives towards nucleophilic substitution reactions ∵ NH2–, NHR– or NR2– are strong bases and thus poor leaving groups

Reaction with Water Amide undergo acid and alkaline hydrolyses to form carboxylic acids and carboxylates respectively Acid hydrolysis: Alkaline hydrolysis:

Amides are dehydrated by heating with P4O10 to form nitriles
35.6 Reactions of the Derivatives of Carboxylic Acids (SB p.55) Dehydration Amides are dehydrated by heating with P4O10 to form nitriles Useful synthetic method for preparing nitriles that are not available by nucleophilic substitution reactions between haloalkanes and cyanide ions

The resulted amines have one carbon less than original amides
35.6 Reactions of the Derivatives of Carboxylic Acids (SB p.55) Hofmann Degradation Amides react with a solution of Br2 in NaOH or a solution of Cl2 in NaOH to give amines through a reaction called Hofmann degradation The resulted amines have one carbon less than original amides Example:

Amides are reduced by LiAlH4 in dry ether to give 1° amines
35.6 Reactions of the Derivatives of Carboxylic Acids (SB p.56) Reduction with Lithium Tetrahydridoaluminate Amides are reduced by LiAlH4 in dry ether to give 1° amines

Acid-catalyzed Hydrolysis
35.6 Reactions of the Derivatives of Carboxylic Acids (SB p.56) Reactions of Esters Acid-catalyzed Hydrolysis Acid-catalyzed hydrolysis of esters is the reverse reaction of esterification Example:

Alkali-catalyzed Hydrolysis
35.6 Reactions of the Derivatives of Carboxylic Acids (SB p.56) Alkali-catalyzed Hydrolysis When esters are refluxed with an alkali such as NaOH, the corresponding alcohol and sodium salt of the carboxylic acid are produced Alkali-catalyzed hydrolysis are irreversible Example:

The reaction is called saponification
35.6 Reactions of the Derivatives of Carboxylic Acids (SB p.57) Soap is made by the alkaline hydrolysis of fats or oils (i.e. triesters) to produce sodium carboxylates (i.e. soap) The reaction is called saponification

Reduction with Lithium Tetrahydridoaluminate
35.6 Reactions of the Derivatives of Carboxylic Acids (SB p.57) Reduction with Lithium Tetrahydridoaluminate Esters are reduced to alcohols by LiAlH4 Example:

Example 35-5 Draw the structural formulae of the missing compounds A to M: (a) (b) (c) Solution: (a) (b) (c) Answer

Example 35-5 Draw the structural formulae of the missing compounds A to M: (d) (e) (f) Solution: (d) (e) (f) Answer

Example 35-5 Draw the structural formulae of the missing compounds A to M: (g) (h) (i) Solution: (g) (h) (i) Answer

Benzoic acid and its sodium salt used as food preservatives
35.7 Uses of Carboxylic Acids and their Derivatives (SB p.59) As Food Preservatives Benzoic acid and its sodium salt used as food preservatives Prevent the microbial growth and spoilage Used in oyster sauce, fish sauce, ketchup, non-alcoholic beverages, fruit juices, margarine, salad dressings, jams and pickled products

As Raw materials for Making Polymers
35.7 Uses of Carboxylic Acids and their Derivatives (SB p.59) As Raw materials for Making Polymers Nylon-6,6, ,is a condensation polymer It is a polyamide made by adding NaOH containing hexanedioyl dichloride and hexane-1,6-diamine to CH3CCl3

Not attack by insects easily
35.7 Uses of Carboxylic Acids and their Derivatives (SB p.60) Advantages of Nylon-6,6 Drip dry easily Not attack by insects easily Resist creasing (no ironing required after washing) Used for making ropes, thread, cords, and various kinds of clothing from stockings to jackets

35.7 Uses of Carboxylic Acids and their Derivatives (SB p.60)
Terylene, , is a polyester made from acid-catalyzed condensation polymerization of benzene-1,4-dicarboxylic acid and ethane-1,2-diol Terylene is used to make wash- and-wear garments

As Solvents Liquid esters are widely used as solvents for all-purpose adhesives, thinners for paints and nail varnish removers

Volatile esters often have characteristic sweet and fruity smells
35.7 Uses of Carboxylic Acids and their Derivatives (SB p.60) As Flavourings Volatile esters often have characteristic sweet and fruity smells They are used as artificial flavourings in food-processing industry An artificial flavouring made of esters

Some esters and their characteristic flavours Structure of ester Characteristic flavour Banana Apple Apricot Pineapple

Some esters and their characteristic flavours (cont’d) Structure of ester Characteristic flavour Rum Grape Wintergreen

The END

Carboxylic Acids and their Derivatives

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