1. P.M. Jadhav
Assistant Professor
Dept. of Chemistry
M.S.P. Mandals, Shri Muktanand
college,
Gangapur, Dist: Aurangabad.

2. The combination of a carbonyl group and a hydroxyl on the same carbon atom is
called a carboxyl group. Compounds containing the carboxyl group are called
carboxylic acids. The carboxyl group is one of the most widely occurring functional
groups in organic chemistry.
C
O
OH C
O
OH
Carbonyl group Hydroxyl group Carboxyl group

3. Carboxylic acids are classified according to the substituent that is attached to the
carboxyl carbon.
 Aliphatic Carboxylic acids: Carboxylic acids have an alkyl group bound to the
carboxyl group is known as aliphatic carboxylic acids. The general formula of an
aliphatic carboxylic acid is R-COOH.
 Aromatic Carboxylic acids: Carboxylic acids have an aryl group bound to the
carboxyl group is known as aromatic carboxylic acids. The general formula of an
aliphatic aromatic carboxylic acid is Ar-COOH.
H3C C
O
OHH C
O
OH H3C CH2 C
O
OH
Formaic acid Acetic acid Propanoic acid
H3C CH2 CH2 C
O
OH
Butanoic acid
COOH COOH
OH
Benzoic acid Salicyclic acid
COOH
COOH
Phthalic acid
COOH
COOH
Terephthalic acid

4. 1. Common Names: Several aliphatic carboxylic acids have been known by their
common names according to source of origin.
2. IUPAC Names: IUPAC names of straight chain aliphatic carboxylic acids are
derived by replacing e of the corresponding alkane by the suffix –oic acid. They are
named as alkanoic acids.
Molecule Origin Formula
Formic acid Extracted from Formica HCOOH
Acetic acid Isolated from vinegar (acetum) CH3COOH
Butyric acid Found in butter. C3H7COOH
Formula Structure Common
name
IUPAC name
CH2O2 HCOOH Formic acid Methanoic acid
C2H4O2 CH3COOH Acetic acid Ethanoic acid
C3H6O2 CH3CH2COOH Propanoic acid Propanoic acid
C4H8O2 CH3CH2CH2COOH Butyric acid Butanoic acid

5.  A carboxylic acid may dissociate in water to give a proton and a carboxylate ion.
Dissociation of a carboxylic acid involves breaking an O-H bond gives a
carboxylate ion with the negative charge spread out equally over two oxygen
atoms, compared with just one oxygen atom in an alkoxide ion. The delocalized
charge makes the carboxylate ion more stable therefore; dissociation of a
carboxylic acid to a carboxylate ion is less endothermic.
 The substituent attached to the carboxyl group of carboxylic acid influence the
acidity of carboxylic acids. The electronic factors such as inductive effect,
resonance effect and hydrogen bonding exerted by the substituents affect on the
acid strength of carboxylic acid.
R C
O
OH R C
O
O H R C
O
O
R C
O
O
Carboxylate ion
Resonance structure
Carboxylic acid

6.  1. Oxidation: The oxidation of aldehyde with oxidizing agents such as CrO3 to
forms carboxylic acids containing the same numbers of carbon atoms with a
oxidizing agents like chromic acid, chromium trioxide. The silver oxide (Ag2O) in
aqueous ammonia solution (Tollen’s reagent) is mild reagent give good yield at
room temperature. E.g. Acetaldehyde reacts with CrO3 in aqueous acid to give
acetic acid.
 2. Grignard reagents (from CO2): Carboxylic acid can be prepared by the
reaction of Grignard reagent (alkyl magnesium halide) with carbon dioxide (CO2)
in presence of dry ether. Grignard reagents react with carbon dioxide to forms a
magnesium carboxylates which on hydrolysis by dilute HCl produces carboxylic
acids.
C
O
HH3C
Acetaldehyde
CrO3 C
O
OHH3C
Acetic acid
H2O
RMgX C O
O
R C
O
OMgX
HCl
R C
O
OH Mg(X)Cl
Grignard
reagent
Carbon dioxide Carboxylic acid

7.  3. Hydrolysis of nitrile: The hydrolysis of nitrile or cyanide in presence of dilute
acid to forms a carboxylic acid. In this reaction –CN group is converted to a –
COOH group.
 4. Hydrolysis Reactions: All the carboxylic acid derivatives (ester, acid
anhydride, acid chloride, amide) can be hydrolyzed into the carboxylic acid in the
acidic or basic media; the hydrolysis reaction is fast and occurs in presence of
water with no acid or base catalyst.
R C R COOH2H2O
H+
Carboxylic acid
N
HCl
Alkyl nitrile
NH3
R C
O
Y R C
O
OHH2O
Carboxylic acid
derivative
Carboxylic acid
H+
Y= -X, -NH2, -OCOR, -OR

8.  Low molecular weights carboxylic acids are colourless liquid at room
temperature i.e. lower member ate liquid up to C9 and have characteristic
odors whereas higher members are solid.
 Carboxylic acids are polar organic compound. Low molecular weight
carboxylic acids (first four members) are soluble in water whereas
solubility in water decrease as molecular weight and chain lengthing
increases.
 Aromatic acids are insoluble in water.
 Carboxylic acids have higher melting and boiling point due to their
capacity to readily form stable hydrogen-bonded dimers.

9.  1) Decarboxylation: The reaction in which salt of carboxylic acid on heating
with soda lime (NaOH + CaO), loses CO2 to give a product alkanes is called a
decarboxylation. Decarboxylation of the most carboxylic acid is exothermic and
is slow reaction.
 2) Ester formation: Reaction of a carboxylic acid with an alcohol under acidic
conditions produces an ester. Esterification is carried out by warming a mixture of
a carboxylic acid and an alcohol in the presence of a strong acid catalyst. The
excess of alcohol used in the esterification reaction. The acid-catalyst can be
provided by strong mineral acids such as H2SO4, HCl and H3PO4 and dehydrating
agent zinc chloride (ZnCl2).
R C
O
ONa
Sodium salt of
carboxylic acid
(NaOH + CaO)
Soda lime
RH CO2
Heat
Alkane
R C
O
OH R' OH
Carboxylic acid Alcohol
R C
O
OR' H2O
Ester
H2SO4

10.  3) Reduction: The reduction of carboxylic acid leads to the formation of primary
alcohols. This reduction carried out using strong reducing agents like Lithium
aluminum hydride (LiAlH4). The aldehyde is an intermediate in this reduction,
but it cannot be isolated because it is reduced more easily than the acid.
 4) Synthesis of Acid Chlorides: The acid chlorides forms by the reaction of a
carboxylic acid with thionyl chloride (SOCl2), phosphorous pentachloride (PCl5)
or oxalyl chloride (COCl)2. The reaction of thionyl chloride with carboxylic acid
to gives acetyl chloride and produces SO2 while in phosphorous pentachloride
reaction produce HCl and the oxalyl chloride reaction produces HCl, CO, and
CO2 gaseous.
R C
PCl5 / SOCl2 / (COCl)2
O
OH
Carboxylic acid
R C
O
Cl
Acid chloride
R COOH
LiAlH4
Dry ether
R CH2 OH
Carboxylic acid Alcohol

11.  5) Amide Formation: The acid chlorides form by the reaction of a carboxylic
acid with thionyl chloride or phosphorous pentachloride which when react with
ammonia to give amide.
 6) Hell-Volhard Zelinsky Reaction: When the carboxylic acid on treatment
with bromine and catalytic amount of phosphorus to give selective product α-
bromo carboxylic acid (2-bromo acid), the α-hydrogen atom is replaced by the
halogen is known as Hell-Volhard Zelinsky Reaction. The reaction in which the
hydrogen atom of an carboxylic acid replaces with a halogen atom on the α-
carbon of a carboxylic acid.
R C
PCl5
O
OH
Carboxylic acid
R C
O
Cl
Acid chloride
NH3 HClR C
O
NH2
Amide
R CH2 C
O
OH
Carboxylic acid
R CH C
O
OH
Br2
Red P
Br
2-Bromo acid

12.  Acrylic acid is the simplest unsaturated carboxylic acid with both double bond
and carbonyl group attached to same carbon atom.
 It is valuable and commonly used chemical intermediate.
 It is also known as 2-Propenoic acid. It was first prepared by the air oxidation of
acrolein.
H2C CH C
O
OH
Acrylic acid

13.  1. Oxidation of acrolein: The air oxidation of acrolein in presence of metal oxide
catalyst like V2O5 /MoO3, Ag2O, to give acrylic acid.
 2.From Epoxide: Ethylene oxide on heating with hydrogen cyanide to give
ethylene cyanohydrin which on hydrolysis give β-hydroxy propionic acid
followed by heating gives acrylic acid.
H2C CH CHO
V2O5 / MoO3
H2C CH COOH
Acrolein Acrylic acid
O2
Heat
CH2
O
H2C
HCN CH2 CH2HO CN
Ethylene cyanohydrin
Ethylene oxide
C
O
OHCH2CH2HO
3-Hydroxy propionic acid
H+
HCl
-H2O
H2C CH C
Acrylic acid
O
OH

14.  3. β-hydroxy carboxylic acid (β-hydroxy propionic acid) on heating to give
acrylic acid.
 4. The reaction of α or β-halo carboxylic acid with alc. KOH or NaOH to give
acrylic acid. E.g. 2-chloropropionic acid and 3-bromopropionic acid react with
alc.KOH to give acrylic acid.
C
O
OHCH2CH2HO
Dehydration
H2OH2C CH C
Acrylic acid
O
OH
Heat
3-Hydroxy propionic acid
C
O
OHCH2CH2Br H2C CH C
Acrylic acid
O
OH
3-Bromo propionic acid
alc. NaOH

15.  1. Diels-Alder Reaction: Acrylic acid is acts as dienophile in the Diels-Alder
reaction. The varietes of dienes undergo cycloaddition reaction with acrylic acid
to give Diel-Alder adduct.
 2. Oxidation: The oxidation of acrylic acid to give glyceric acid as intermediate
product which further oxidized to give oxalic acid.
Acrylic acid
CH2
HC
HC
CH2
1,3-Butadiene
CH2
HC
COOH COOH
Diels-Alder addcut
H2C CH C
O
OH
Acrylic acid
H2C CH C
O
OH
OHOH
Glyceric acid
HO C C
O
OH
O
Oxalic acid
OxidationOxidation

16.  3. Addition Reactions: The double bond in acrylic acid acts as Michael
acceptor and which undergo addition reaction to give different product. The
reaction in which addition reaction of acrylic acid with a compound with active
methylene group such as malonic ester, acetoacetic ester and cyanoacetic ester
in presence of a base.
H2C CH C
O
OH
Acrylic acid
CH2(COOCH3)2
C2H5ONa
CH CH2 CH2 C
O
OHH3COOC
COOCH3
Dimethyl malonate

17.  Carboxylic acids containing two carboxyl groups are called dicarboxylic
acids.
 They are named by adding dioic acid as a suffix to the name of the
corresponding hydrocarbon. Both the carboxyl carbon atoms are numbered
as a part of the main chain.
CH
CH2
COOH
COOH
OH
Malic acid
C
C
OH
OH
H
COOH
H
COOH
Tartaric acid
COOH
COOH
Ethanedioic acid
(Oxalic acid)
CH2
COOH
COOH
Propanedioic acid
(Malonic acid)
CH2
CH2
COOH
COOH
Butanedioic acid
(Succinic acid)

18. Preparation:
 1. The reaction of bromosuccinic acid with moist silver oxide to give malic
acid.
 2. The tartaric acid on partial reduction in presence of hydroiodic acid to
give malic acid.
CH
CH2
COOH
COOH
HO
Malic acid
CH
CH2
COOH
COOH
HO
Malic acid
AgOH
CH
CH2
COOH
COOH
Br
Bromosuccinic acid
2HI
CH
CH
COOH
COOH
HO
HO
Tartaric acid
CH
CH2
COOH
COOH
HO
Malic acid

19.  Malic acid is soluble in water, alcohol and sparingly soluble in ether.
 It is colourless crystalline solid.
 Malic acid exhibits optical isomerism as it contains chiral carbon hence
exists in two optically active and one inactive form.
C
CH2
H
COOH
HO
L-(-)-Malic acid
COOH
C
CH2
OH
COOH
H
COOH
D-(+)-Malic acid

20.  1. Malic acid when heated at 150-180°C it gives a mixture of fumaric
acid and maleic anhydride.
 2. Malic acid on oxidation with mild oxidizing reagent it is converted to
oxaloacetic acid.
CH
CH2
COOH
COOH
HO
Malic acid
C
C
COOH
HOOC
H
H
Fumaric acid
C
C
COOH
H
H
COOH
Maleic acid
C
C
C
H
H
C
O
O
O
Maleic anhydride
-H2O
-H2O
-H2O
Heat
Heat
CH
CH2
COOH
COOH
HO
Malic acid
Oxidation
(O) C
CH2
COOH
COOH
O
Oxaloacetic acid

21. Preparation
1. The reaction of glyoxal with HCN to give glyoxal cyanohydrin which on
hydrolysis to give tartaric acid.
C
C
OH
OH
H
COOH
H
COOH
Tartaric acid
CHO
CHO
2HCN C
C
CN
CN
H
H OH
OH
H2O
H+ C
C
OH
OH
H
COOH
H
COOH
Tartaric acid
Glyoxal

22. 2. Hydroxylation of maleic and fumaric acids: Maleic acid on oxidation with
alkaline KMnO4 gives meso-tartaric acid whereas oxidation of fumaric acid with
alkaline KMnO4 to gives (±)-tartaric acid.
3. Naturally occurring tartaric acid is dextro rotatory and is potassium salt present
in the various fruits such as grapes, plums and argol. In the fermentation of grape
juice, the potassium hydrogen tartarate deposits as a reddish brown crust (argol)
which on crystallization, argol deposits crystals of the salt known as cream of
tartar.
C
C
COOH
H
H
COOH
Maleic acid
H2O
C
C
OH
OH
H
COOH
H
COOH
Meso-Tartaric acid
H2O
C
C
COOH
HOOC
H
H
Fumaric acid
KMnO4
C
C
OH
OH
H
COOH
H
COOH
Tartaric acid
C
C
OH
H
H
COOH
CH
CH
C
HO
HO
C
O
O
OHO
COOK
O
Ca
Calcium tartarate
CH
CH
COOK
HO
HO
COOK
Potassium tartarate
Ca(OH)2
2H2O
Cream of tartar

23.  Malic acid is water soluble in water, alcohol but insoluble in ether.
 It is colourless crystalline solid. Tartaric acid exhibits optical isomerism as
it contains two similar chiral carbons hence exists in two optically active
enantiomeric form and meso form.
 Chemically all the three forms behave in the same way.
 Tartaric acid behaves as a dicarboxylic acid as well as secondary alcohol.

24.  1. Action of Heat: The tartaric acid when heated at 1500C to give tartaric
anhydride.
 The tartaric acid on strong heating above its melting point to gives pyruvic acid.
 The tartaric acid when heated with cone. H2SO4, it decomposes to CO2, CO and
H2O.
CH
CH
C
HO
HO
C
O
O
O
CH
CH
COOH
HO
HO
COOH
Heat
1500
C
Tartaric acid
Tartaric anhydride
C COOH H2OH3C
CH
CH
COOH
HO
HO
COOH
Strong heating
Tartaric acid
CO2
O
Pyruvic acid
3H2O
CH
CH
COOH
HO
HO
COOH
Tartaric acid
CO2CO
Conc.H2SO4
Heat

25. 2. Reduction: The reduction of tartaric acid with hydroiodic to give malic acid
which further reduced to give succinic acid.
3. Oxidation: The oxidation of tartaric acid with HNO3 to form tartonic acid which
further oxidized to give oxalic acid.
 When the tartaric acid is oxidized with Fenton’s reagent to gives dihydroxy
fumaric acid.
4. Complex formation: Sodium potassium tartarate forms complex with Cu2+.
CH
CH2
COOH
COOH
HO
Malic acid
CH
CH
COOH
HO
HO
COOH
Tartaric acid
CH2
CH2
COOH
COOH
Succinic acid
HI HI
CH
COOH
COOHHO
Tartonic acid
CH
CH
COOH
HO
HO
COOH
Tartaric acid
COOH
COOH
Oxalic acid
(O) (O)
HNO3HNO3
C
C
COOH
HOOC
HO
OH
Dihydroxy fumaric acid
CH
CH
COOH
HO
HO
COOH
Tartaric acid
H2O2 / FeSO4
C
C
OH
OH
H
COOK
H
COONa
C
C
COO K
COO Na
O
Sodium potassium tartarate
Cu2+
O
H
H
Cu
Fehling's solution complex

26.  Preparation: Citric acid is prepared by the fermentation of sugars (Cane-Sugar,
glucose) or by the fermentation of dilute solution of molasses in the presence of
certain micro-organisms. Citric acid is also manufactured from the citrus fruit
wastes.
C
CH2
COOH
COOH
HO
Citric acid
CH2 COOH

27.  Citric acid is colourless crystalline solid.
 It is soluble in water and alcohol and sparingly soluble in ether.
 A molecule of citric acid contains one tertiary hydroxyl group and three
carboxyl groups.
 Citric acid exhibits the properties of both alcohol and carboxylic acid.

28.  1. The citric acid on treatment with acetyl chloride forms monoacetyl derivative
acetylcitric acid. The reaction takes place on hydroxyl group of citric acid.
 2. Reduction: The reduction of citric acid with HI to forms tricarballylic acid.
The reaction takes place on hydroxyl group of citric acid.
C
CH2
OCOCH3
COOH
HOOC
Acetylcitric acid
CH2 COOH
C
CH2
HOOC
COOH
OH
Citric acid
CH2 COOH
CH3COCl
HC
CH2
COOH
COOH
Tricarballylic acid
CH2 COOH
C
CH2
COOH
COOH
HO
Citric acid
CH2 COOH
HI

29.  3. Salt formation: The citric acid forms a trisodium citrate when treated with the
alkali such as NaOH.
 4. Effect of heat: When citric acid is heated to 150°C it gives β-hydroxy
unsaturaed acid (aconitic acid) with removal of water molecule.
C
CH2
COOH
COOH
HO
Citric acid
CH2 COOH
NaOH
C
CH2
COOH
COOH
HO
Monosodium citrate
CH2 COO Na
C
CH2
COOH
COO Na
HO
CH2 COO Na
NaOH
NaOH
C
CH2
COO Na
COO Na
HO
CH2 COO Na
Trisodium citrate
Disodium citrate
C
CH2
COOH
COOH
HO
Citric acid
CH2 COOH
Heat
C
CH2
COOH
COOH
CH COOH
H2O
Aconitic acid
150°C