3. Methanoic acid
Total of one
carbon atom
(meth-)
C0H1COOH
Ethanoic acid
Total of two
carbons atoms
(eth-)
C1H3COOH
Propanoic acid
Total of three
carbon atoms
(propan-)
C2H5COOH
*Take note of the functional group’s location, highlighted by the
dotted box
4. Replace the ‘e’ with ‘oic acid’ at the end of
the name of the hydrocarbon
Example:
H H
H C C H
H H
ethane
H O
H C C O H
H
ethanoic acid
5. Since these are acidic compounds, therefore easily
lose H+ ion and covert in carboxylate ion (RCOO-)
6. Hence carboxylic acids can be represented by to
resonance structures.
COOH is less electrophile than aldehyde and
ketone.
120̊̊
planer structure
sp2 hybridized
7. 1. From primary alcohol and
aldehyde(O)
2. From alkyl benzene(O)
3. From Nitriles and amides ( by
hydrolysis)
4. From Dry ice( by carboxylation of
Grignard reagent)
5. From acyl chlorides and acid
anhydrides( by hydrolysis)
6. From esters ( by hydrolysis)
17. Ethanoic acid(acetic acid) is the most
important organic acid
It is used in vinegar as preservative and
flavourings.
18.
19.
20.
21. Making of drugs, dyes, paints, insecticides,
plastics.
Making of esters.
22. Organic
acid
Where it is found
Lactic acid Sour milk
Oxalic acid Rhubarb plant
Citric acid Limes, lemons
Formic acid Insect bites
Tartaric
acid
Grape juice
Acetic acid Vinegar
Malic acid Apples and pears