
Phenol does not decompose $NaHC{O_3}$ to evolve but picric acid does.
A.True
B.False
Answer
555.9k+ views
Hint: Acids react with sodium hydrogen carbonate to evolve carbon dioxide. The compounds which are more acidic than carbonic acid will react with \[NaHC{O_3}\] else the reaction would not take place.
Complete Step by step answer: Phenol is acidic in nature . But it is a weak acid. The presence of $ - OH$ on phenol and the conjugation of electrons in benzene rings pull the electrons away from the $ - OH$ group . Sodium bicarbonate is a weak base . It easily accepts electrons from stronger acids like carbonic acid, but it is not strong enough to pull the proton off phenol. Hence, due to the weak acidic nature of phenol \[NaHC{O_3}\] does not react with phenol .
We will see whether it reacts with picric acid or not.
$2,4,6 - trinitrophenol$ is commonly known as picric acid.
The presence of three nitro groups at ortho-para positions increases the acidity of the compound. It is an electron withdrawing group . EWG ( electron withdrawing group ) increases the acidic character of any compound. And hence picric acid becomes a stronger acid than phenol and carbonic acid. It is actually as strong as hydrochloric acid. Since any acid stronger than carbonic acid can react with $NaHC{O_3}$ and give effervescence of $C{O_2}$.
Hence, picric acid reacts with sodium bicarbonate to give effervescence of carbon dioxide while phenol does not.
The correct option A is TRUE.
Note: This can be seen as a general reaction between an acid and a base. Only the acids that can readily donate protons can react with it. Phenol is less acidic than both picric acid as well as carbonic acid.
Complete Step by step answer: Phenol is acidic in nature . But it is a weak acid. The presence of $ - OH$ on phenol and the conjugation of electrons in benzene rings pull the electrons away from the $ - OH$ group . Sodium bicarbonate is a weak base . It easily accepts electrons from stronger acids like carbonic acid, but it is not strong enough to pull the proton off phenol. Hence, due to the weak acidic nature of phenol \[NaHC{O_3}\] does not react with phenol .
We will see whether it reacts with picric acid or not.
$2,4,6 - trinitrophenol$ is commonly known as picric acid.
The presence of three nitro groups at ortho-para positions increases the acidity of the compound. It is an electron withdrawing group . EWG ( electron withdrawing group ) increases the acidic character of any compound. And hence picric acid becomes a stronger acid than phenol and carbonic acid. It is actually as strong as hydrochloric acid. Since any acid stronger than carbonic acid can react with $NaHC{O_3}$ and give effervescence of $C{O_2}$.
Hence, picric acid reacts with sodium bicarbonate to give effervescence of carbon dioxide while phenol does not.
The correct option A is TRUE.
Note: This can be seen as a general reaction between an acid and a base. Only the acids that can readily donate protons can react with it. Phenol is less acidic than both picric acid as well as carbonic acid.
Recently Updated Pages
Master Class 11 Economics: Engaging Questions & Answers for Success

Master Class 11 English: Engaging Questions & Answers for Success

Master Class 11 Social Science: Engaging Questions & Answers for Success

Master Class 11 Biology: Engaging Questions & Answers for Success

Class 11 Question and Answer - Your Ultimate Solutions Guide

Master Class 11 Business Studies: Engaging Questions & Answers for Success

Trending doubts
What is meant by exothermic and endothermic reactions class 11 chemistry CBSE

10 examples of friction in our daily life

One Metric ton is equal to kg A 10000 B 1000 C 100 class 11 physics CBSE

Difference Between Prokaryotic Cells and Eukaryotic Cells

What are Quantum numbers Explain the quantum number class 11 chemistry CBSE

1 Quintal is equal to a 110 kg b 10 kg c 100kg d 1000 class 11 physics CBSE

