



The carbocation fromed is very unstable. Therefore, it is inactive towards SN1 as halogen is attached to bridge head carbon atom, where formation of carbocation is not possible.
So, the correct answer is (C).
Match the LIST-I with LIST-II: 
Choose the correct answer from the options given below:
CH$_3$–Br $\xrightarrow{\text{CH$_3$OH/Nu}}$ CH$_3$OH
Correct order of rate of this reaction for given nucleophile:

In the following \(p\text{–}V\) diagram, the equation of state along the curved path is given by \[ (V-2)^2 = 4ap, \] where \(a\) is a constant. The total work done in the closed path is: 
Let \( ABC \) be a triangle. Consider four points \( p_1, p_2, p_3, p_4 \) on the side \( AB \), five points \( p_5, p_6, p_7, p_8, p_9 \) on the side \( BC \), and four points \( p_{10}, p_{11}, p_{12}, p_{13} \) on the side \( AC \). None of these points is a vertex of the triangle \( ABC \). Then the total number of pentagons that can be formed by taking all the vertices from the points \( p_1, p_2, \ldots, p_{13} \) is ___________.
Consider the following two reactions A and B: 
The numerical value of [molar mass of $x$ + molar mass of $y$] is ___.
The hydrocarbons such as Haloalkanes and Haloarenes are the ones, in which one or more hydrogen atoms are replaced with halogen atoms. The main difference between Haloalkanes and Haloarenes is that Haloalkanes are derived from open chained hydrocarbons, also called alkanes, and Haloarenes are derived from aromatic hydrocarbons.