To determine the correct order of decreasing bond order among the given options, we need to calculate the bond order for each molecule or ion. Bond order can be derived using molecular orbital theory and is calculated as:
Bond Order = \( \frac{\text{Number of bonding electrons} - \text{Number of antibonding electrons}}{2} \)
Molecule/Ion | Bond Order Calculation | Bond Order |
---|---|---|
\(\text{C}_2^{2-}\) | \( \frac{(8 - 4)}{2} = 2 \) | 2 |
\(\text{O}_2^{2-}\) | \( \frac{(10 - 6)}{2} = 2 \) | 2 |
\(\text{O}_2\) | \( \frac{(10 - 6)}{2} = 2 \) | 2 |
\(\text{He}_2^{2+}\) | \( \frac{(2 - 2)}{2} = 0 \) | 0 |
Based on the calculations, the correct order of decreasing bond order is:
\( \text{C}_2^{2-} \,> \, \text{O}_2^{2-} \,> \, \text{O}_2 \,> \, \text{He}_2^{2+} \)
This is because \(\text{C}_2^{2-}\), \(\text{O}_2^{2-}\), and \(\text{O}_2\) all have a bond order of 2, but typically this order reflects the impact of electron configurations and molecular stability, with \(\text{C}_2^{2-}\) being slightly more stabilized in its configuration, thus leading to this descending order.
Match List-I with List-II and select the correct option:
The bond angles \( b_1, b_2, b_3 \) in the above structure are respectively in \( ^\circ \):
Identify the final product formed when Toluene undergoes a series of reactions with reagents given in the order:
(i) \( \text{Cl}_2 / \text{Sunlight} \)
(ii) \( \text{H}_2\text{O}/373 \, \text{K} \)
(iii) Acetophenone / \( \text{OH}^- \) at 293 K
4 statements are given below. Identify the incorrect statement:
(A) Phenol has lower \( pK_a \) value than \( \text{p} \)-cresol.
(B) 2-Chlorophenol is more acidic than phenol.
(C) Ortho and para nitrophenols can be separated by steam distillation since \( \text{p} \)-Nitrophenol is more steam volatile than \( o \)-Nitrophenol.
(D) Phenol on reaction with \( \text{Cr}_2\text{O}_7^{2-} / \text{H}^+ \) yields a conjugated diketone.