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.
The correct increasing order of stability of the complexes based on \( \Delta \) value is:
Match List-I with List-II: List-I
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 |
Let one focus of the hyperbola $ \frac{x^2}{a^2} - \frac{y^2}{b^2} = 1 $ be at $ (\sqrt{10}, 0) $, and the corresponding directrix be $ x = \frac{\sqrt{10}}{2} $. If $ e $ and $ l $ are the eccentricity and the latus rectum respectively, then $ 9(e^2 + l) $ is equal to:
The largest $ n \in \mathbb{N} $ such that $ 3^n $ divides 50! is: