Advertisements
Advertisements
Question
Arrange the following carboxylic acids with increasing order of their acidic strength and justify your answer.
1) ![]()
2) ![]()
3) ![]()
Advertisements
Solution
- Increasing order of their acidic strength: 2 > 3 > 1.
- Oxygen atom is electronegative and exerts electron withdrawing inductive effect (–I effect).
- Thus, compound (2) and (3) are more acidic as compared to (1).
- However, the inductive effect decreases as the oxygen in the ring moves away from the carboxyl group. Therefore, compound (3) is less acidic than compound (2).
APPEARS IN
RELATED QUESTIONS
Answer in brief.
Formic acid is stronger than acetic acid. Explain.
Write the structure of the product formed when carboxylic acid is heated with a dehydrating agent like P2O5
Write the preparation reactions for acid amide from the following.
Carboxylic acid
Write the preparation reactions for acid amide from the following.
Acid chloride
Write reactions for the following conversions.
Propanone to Propane
Write chemical reactions to convert –COOH group of acetic acid into the following.
C2H5OH
Write reaction for preparation of acetophenone from benzoyl chloride.
Explain the acidic nature of carboxylic acids.
Write reactions for the action of the following reagents on p-chlorobenzaldehyde.
Ethane-1,2-diol in presence of dry HCl.
Which of the following compounds reacts with ammonia to form urotropine?
The product of the reaction between dialkyl cadmium and acyl chloride is a/an ____________.
In the following reaction:

The product X is:
A flavouring agent found in oil of wintergreen is ______.
The reducing agent preferred to convert carboxylic acids and esters to primary alcohols is ____________.
Which among the following is the strongest acid?
Which of the following compounds is obtained when ethanoic anhydride is treated with water?
Write structure of adipic acid.
Which oxide of nitrogen is obtained on heating ammonium nitrate at 250°C?
Excess of ammonia with sodium hypochloride solution in the presence of glue or gelatine gives ______.
Which of the following can reduce?
\[\ce{RCOOH -> RCH2OH}\]
Draw structures 01 conjugate bases of monochloroacetic acid and dichloroacetic acid. Which one is more stabilized by -I effect?
Which of the following represents the correct order of the acidity in the given compounds?
Which among the following is the strongest acid?
