Write the correct order of rate of reaction of following with PhN$_2$Cl 
The rate of reaction with PhN$_2$Cl (azo coupling) is affected by substituents on the aromatic ring. Electron-donating groups (EDGs) increase the electron density of the ring, making it more nucleophilic and increasing the rate.
1. R has an NH$_2$ group, which is a strong EDG (+M effect).
2. P has a CH$_3$ group, which is a weak EDG (+I and hyperconjugation).
3. Q has an NO$_2$ group, which is a strong electron-withdrawing group (-M effect).
Thus, the correct order of reaction rate is R>P>Q.
Write the correct order of rate of reaction of following compounds with $PhN_2Cl$
P: $N,N$-dimethylaniline
Q: $N,N$-dimethyl-3-methylaniline
R: $N,N$-dimethyl-2,6-dimethylaniline
Most preferred site for electrophilic substitution in above example?
(Note: The molecule contains a nitrogen-containing ring and a carbonyl-containing ring, labels are U, S, R, P).
| Column-I (Complex compound) | Column-II ($\Delta_0$ (CFSE) $\text{cm}^{-1}$) |
| (i) $[Cr(CN)_6]^{3-}$ | (P) 17000 |
| (ii) $[Cr(H_2O)_6]^{3+}$ | (Q) 15000 |
| (iii) $[Cr(en)_3]^{3+}$ | (R) 12000 |
| (iv) $[CrF_6]^{3-}$ | (S) 20000 |
Identify A in the following reaction. 
For the reaction, \(N_{2}O_{4} \rightleftharpoons 2NO_{2}\) graph is plotted as shown below. Identify correct statements.
A. Standard free energy change for the reaction is 5.40 kJ \(mol^{-1}\).
B. As \(\Delta G\) in graph is positive, \(N_{2}O_{4}\) will not dissociate into \(NO_{2}\) at all.
C. Reverse reaction will go to completion.
D. When 1 mole of \(N_{2}O_{4}\) changes into equilibrium mixture, value of \(\Delta G = -0.84 \text{ kJ mol}^{-1}\).
E. When 2 mole of \(NO_{2}\) changes into equilibrium mixture, \(\Delta G\) for equilibrium mixture is \(-6.24 \text{ kJ mol}^{-1}\).
Choose the correct answer from the following.

Assuming in forward bias condition there is a voltage drop of \(0.7\) V across a silicon diode, the current through diode \(D_1\) in the circuit shown is ________ mA. (Assume all diodes in the given circuit are identical) 
Write the correct order of rate of reaction of following compounds with $PhN_2Cl$
P: $N,N$-dimethylaniline
Q: $N,N$-dimethyl-3-methylaniline
R: $N,N$-dimethyl-2,6-dimethylaniline
Most preferred site for electrophilic substitution in above example?
(Note: The molecule contains a nitrogen-containing ring and a carbonyl-containing ring, labels are U, S, R, P).