JEE syllabus
Carboxylic acids:
Preparation, properties
Characteristic reactions
formation of esters,
acid chlorides and amides,
ester hydrolysis;
---------
1. Carboxylic acids are the compound containing carboxyl group in their molecules.
-C with a double bond with oxygen and single bond with OH
2. These acids can be aliphatic or aromatic.
aliphatic acids:
Formic acid HCOOH
Acetic acid CH-3COOH
Isobutyric acid (Branched)
aromatic acids
Bezoic acid : H in benzene substituted by COOH
m-Nitrobenzoic acid: One more H substituted by NO-2
o-Toluic acid (o refers to ortho) Benzoic acid with one more H substituted by CH-3
3. Methods of Preparation of Monocarboxylic Acids:
1. From oxidation of primary alcohols
2. By oxidation of aldehydes and ketones.
A. Reactions due to hydrogen atom of carboxyl group
1. Acidic character
a. Action with blue litmus
all carboxylic acids turn blue litmus red.
b. Reaction with metals: liberation of hydrogen
Carboxylic acids react with active metals such as Na, K, Ca, Mg, Zn, etc., to form their salts with the liberation of hydrogen.
c. Action with alkalies: formation of salts
Carboxylic acids neutralize alkalies forming salts and water.
d. Action with carbonates and bicarbonates: evolving carbon dioxide
Carboxylic acids decompose carbonates and bicarbonates evolving carbon dioxide with brisk effervescence.
Mechanism of acidic character
In the COOH group due to resonance in the OH, O acquires some positive charge the electron pair of OH is drawn towards O. This displacement of electrons causes the release of a proton and a carboxylate ion, RCOO- is formed. This is the reason for acidic character of carboxylic acids.
The strength of acids can be expressed in terms of dissociation constant Ka or Ph number of PKa number which is pKa = -log Ka
A stronger acid will have a higher Ka value but smaller PKa value.
Effects of substituents on acidic strength of acids
Electron releasing substituents: Alkyl is an electron releasing group. If the H atom of formic acid (HCOOH) is replaced by CH3 group to form acetic acid (CH3COOH) the alkyl group will tend to increase the electron density on the oxygen atom of the O-H bond. This increase will make removal H+ ion difficult in comparison to formic acid.
Acetic acid is a weaker acid in comparison to formic acid.
The electron release effect is called +I effect. As +I effect increases, acidic strength will go down. As more alkyl groups are there +I effect increases
CH3
Therefore acidic property is stronger or more for CH3COOH.
Acidic strength is in the following order
acidic strength of HCOOH>CH3COOH>CH3CH2COOH>(CH3)2CHCOOH
Electron withdrawing substituents: Substituents like halogens tend to withdraw the electron charge. Halogens are electron attracting atoms(-I inductive effect). They withdraw the electrons from the carbon to which they are attached and this effect is transmitted throught the chain. The increases positive charge on O atom in the O-H bond and dissociation of H+ ion or proton takes place more easily.
Hence chloroacetic acid is stronger acid than acetic acid.
Some more topics need to be covered
Carboxylic acid - practice questions
http://makoxmcqs.com/chemistry-mcqs-for-jee-main-carboxylic-acids-and-their-derivatives-mcq-practice-sheet/
Updated on 18 January 2020
5 February 2008
Carboxylic acids:
Preparation, properties
Characteristic reactions
formation of esters,
acid chlorides and amides,
ester hydrolysis;
---------
1. Carboxylic acids are the compound containing carboxyl group in their molecules.
-C with a double bond with oxygen and single bond with OH
2. These acids can be aliphatic or aromatic.
aliphatic acids:
Formic acid HCOOH
Acetic acid CH-3COOH
Isobutyric acid (Branched)
aromatic acids
Bezoic acid : H in benzene substituted by COOH
m-Nitrobenzoic acid: One more H substituted by NO-2
o-Toluic acid (o refers to ortho) Benzoic acid with one more H substituted by CH-3
3. Methods of Preparation of Monocarboxylic Acids:
1. From oxidation of primary alcohols
2. By oxidation of aldehydes and ketones.
A. Reactions due to hydrogen atom of carboxyl group
1. Acidic character
a. Action with blue litmus
all carboxylic acids turn blue litmus red.
b. Reaction with metals: liberation of hydrogen
Carboxylic acids react with active metals such as Na, K, Ca, Mg, Zn, etc., to form their salts with the liberation of hydrogen.
c. Action with alkalies: formation of salts
Carboxylic acids neutralize alkalies forming salts and water.
d. Action with carbonates and bicarbonates: evolving carbon dioxide
Carboxylic acids decompose carbonates and bicarbonates evolving carbon dioxide with brisk effervescence.
Mechanism of acidic character
In the COOH group due to resonance in the OH, O acquires some positive charge the electron pair of OH is drawn towards O. This displacement of electrons causes the release of a proton and a carboxylate ion, RCOO- is formed. This is the reason for acidic character of carboxylic acids.
The strength of acids can be expressed in terms of dissociation constant Ka or Ph number of PKa number which is pKa = -log Ka
A stronger acid will have a higher Ka value but smaller PKa value.
Effects of substituents on acidic strength of acids
Electron releasing substituents: Alkyl is an electron releasing group. If the H atom of formic acid (HCOOH) is replaced by CH3 group to form acetic acid (CH3COOH) the alkyl group will tend to increase the electron density on the oxygen atom of the O-H bond. This increase will make removal H+ ion difficult in comparison to formic acid.
Acetic acid is a weaker acid in comparison to formic acid.
The electron release effect is called +I effect. As +I effect increases, acidic strength will go down. As more alkyl groups are there +I effect increases
CH3
Therefore acidic property is stronger or more for CH3COOH.
Acidic strength is in the following order
acidic strength of HCOOH>CH3COOH>CH3CH2COOH>(CH3)2CHCOOH
Electron withdrawing substituents: Substituents like halogens tend to withdraw the electron charge. Halogens are electron attracting atoms(-I inductive effect). They withdraw the electrons from the carbon to which they are attached and this effect is transmitted throught the chain. The increases positive charge on O atom in the O-H bond and dissociation of H+ ion or proton takes place more easily.
Hence chloroacetic acid is stronger acid than acetic acid.
Some more topics need to be covered
Carboxylic acid - practice questions
http://makoxmcqs.com/chemistry-mcqs-for-jee-main-carboxylic-acids-and-their-derivatives-mcq-practice-sheet/
Updated on 18 January 2020
5 February 2008
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