



For SN2, steric hindrance matters: \(1^◦ > 2^◦ > 3^◦\). For SN1, carbocation stability is key. EDGs activate aromatic rings for electrophilic substitution, while EWGs activate for nucleophilic substitution.
In SN2 reactions:
In SN1 reactions:
In electrophilic aromatic substitution:
In nucleophilic aromatic substitution:
(A), (B), (C), and (D) are all correct.
Match List-I with List-II: List-I
The correct increasing order of stability of the complexes based on \( \Delta \) value is:
| List I (Molecule) | List II (Number and types of bond/s between two carbon atoms) | ||
| A. | ethane | I. | one σ-bond and two π-bonds |
| B. | ethene | II. | two π-bonds |
| C. | carbon molecule, C2 | III. | one σ-bonds |
| D. | ethyne | IV. | one σ-bond and one π-bond |

A square loop of sides \( a = 1 \, {m} \) is held normally in front of a point charge \( q = 1 \, {C} \). The flux of the electric field through the shaded region is \( \frac{5}{p} \times \frac{1}{\varepsilon_0} \, {Nm}^2/{C} \), where the value of \( p \) is: