Step 1: Understand the structure of phenol and picric acid.
Picric acid is 2,4,6-trinitrophenol.
Step 2: Recall the nitration of phenol.
Phenol is activated towards electrophilic substitution.
Step 3: Consider the reagents.
Conc. HNO3 is a strong nitrating agent.
Dil. HNO3 leads to mono-nitration.
H2SO4 leads to sulfonation.
Step 4: Identify the correct reagent for picric acid formation.
Concentrated HNO3 nitrates phenol at the 2, 4, and 6 positions.
Step 5: Conclusion.
Conc. HNO3 reacts with phenol to form picric acid.
For the thermal decomposition of \( N_2O_5(g) \) at constant volume, the following table can be formed, for the reaction mentioned below: \[ 2 N_2O_5(g) \rightarrow 2 N_2O_4(g) + O_2(g) \] Given: Rate constant for the reaction is \( 4.606 \times 10^{-2} \text{ s}^{-1} \).
Predict the major product $ P $ in the following sequence of reactions:
(i) HBr, benzoyl peroxide
(ii) KCN
(iii) Na(Hg), $C_{2}H_{5}OH$
If the ratio of the terms equidistant from the middle term in the expansion of \((1 + x)^{12}\) is \(\frac{1}{256}\), then the sum of all the terms of the expansion \((1 + x)^{12}\) is:
A 3 kg block is connected as shown in the figure. Spring constants of two springs \( K_1 \) and \( K_2 \) are 50 Nm\(^{-1}\) and 150 Nm\(^{-1}\) respectively. The block is released from rest with the springs unstretched. The acceleration of the block in its lowest position is ( \( g = 10 \) ms\(^{-2}\) )