ACKNOWLEDGEMENT:
Figure
|
Source of Figure
|
Figure 17b
|
http://www.ck12.org
|
Figure Table 7a
|
http://www.restauro-online.com/
|
Figure Table 7b
|
http://howtosmile.org/
|
Figure Table 7c
|
http://www.wikiwand.com/
|
Figure Table 7d
|
http://www.wikiwand.com/
|
Carboxylic Acids:
Carboxylic acids are naturally occurring acids. They are
weakly ionized in nature. They form a homologous series of organic compounds
with the carboxylic functional group or –COOH. Each successive member of the
series differ by CH2, and the general formula of the series is Cn-1H2n-1COOH. The functional group, –COOH gives the compound its acidic properties and in aqueous solutions, the H radical in –COOH is ionnized to give H+ ions. The H+ ions are responsible for the acid behaviour of the compound.
Figure 17b shows the functional group.
Figure 17b:
Table 7: First 4 carboxylic acids in the carboxyl homologous series
Carboxylic Acid
|
Common name
|
Formula
|
Physical Structure
|
Methanoic Acid
|
Formic Acid
|
H3COOH
|
|
Ethanoic Acid
|
Acetic Acid
(Vinegar)
|
CH3COOH
|
|
Propanoic Acid
|
-
|
C2H5COOH
|
|
Butanoic Acid
|
-
|
C3H7COOH
|
|
Chemical properties
of carboxylic acids:
Carboxylic acids are weak acids, implying that they are only
partially ionized in their aqueous solutions. They, however react with metals,
bases and carbonates like any other acid.
- Carboxylic acids turn moist blue litmus paper to red.
- Reaction with metals:
- Reaction with metal oxides:
- Reaction with metal hydroxides:
- Reaction with metal carbonates:
Acids react with metal carbonates to form salt, water and Carbon dioxide gas.