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प्रश्न
Correct order of acid strength for
- acetic acid
- fluoroacetic acid
- 4-Nitrobenzoic acid
- 4-Methyl benzoic acid is ______.
विकल्प
i > ii > iii > iv
ii > iii > iv > i
iii > iv > i > ii
iv > i > ii > iii
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उत्तर
ii > iii > iv > i
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संबंधित प्रश्न
Answer in brief.
Formic acid is stronger than acetic acid. Explain.
Arrange the following carboxylic acids with increasing order of their acidic strength and justify your answer.
1) 
2) 
3) 
Write the preparation reactions for acid amide from the following.
Carboxylic acid
Write reactions for the following conversions.
Propanone to Propane
Write chemical reactions to convert –COOH group of acetic acid into the following.
CH4
Write chemical reactions to convert –COOH group of acetic acid into the following.
CH3COCl
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.
Complete the following sequence of reactions and write structures for A, B, C.
\[\ce{Dry ice ->[i. Dry ether][ii. Hydrolysis] A ->[PCl5] B ->[H2(gas)][Pd - BaSO4] C}\]
Which of the following compounds reacts with ammonia to form urotropine?
In the reaction, \[\ce{C6H5COCH3 ->[{[H]}][Zn-Hg/conc. HCl] X}\], X is ______.
A flavouring agent found in oil of wintergreen is ______.
Which of the following carboxylic acids will have the highest acidity?
The elimination of CO2 from a carboxylic acid is known as ____________.
The reducing agent preferred to convert carboxylic acids and esters to primary alcohols is ____________.
Which among the following is the strongest acid?
The oxidation number of B in NaBH4 is ____________.
Which of the following functional groups is reduced by diborane?
Which of the following compounds is obtained when ethanoic anhydride is treated with water?
Which of the following carboxylic acids ha highest acidic strength?
The number of bonding pairs and lone pairs of electrons present in the central atom of ammonia molecular are respectively.
Draw structures 01 conjugate bases of monochloroacetic acid and dichloroacetic acid. Which one is more stabilized by -I effect?
Identify the product ‘B’ in the following sequence of reactions.
\[\ce{\underset{}{Methylpropanoate} ->[Δ][dil. NaOH] \underset{\underset{}{}}{A}->[H+][Conc. HCl] \underset{\underset{}{}}{B}}\]
Which of the following can not be oxidised to give carboxylic acid?
Which of the following represents the correct order of the acidity in the given compounds?
