Due to salt formation with AlCl\(_3\), aniline becomes a Lewis base, deactivating the benzene ring.
Step 1: Role of Lewis Acid Catalyst in Friedel-Crafts Reaction - Friedel-Crafts alkylation and acylation require a Lewis acid catalyst like AlCl\(_3\) to generate the electrophile.
Step 2: Interaction Between Aniline and AlCl\(_3\) - Aniline (\( \text{C}_6\text{H}_5\text{NH}_2 \)) has a lone pair on nitrogen, which interacts with AlCl\(_3\), forming a salt. \[ \text{C}_6\text{H}_5\text{NH}_2 + AlCl_3 \rightarrow [\text{C}_6\text{H}_5\text{NH}_2]^+ [AlCl_3]^- \] - This deactivates the benzene ring, making it less reactive toward electrophilic substitution.
Step 3: Conclusion Due to this salt formation, aniline does not undergo Friedel-Crafts reaction.





Consider the following reaction of benzene. the percentage of oxygen is _______ %. (Nearest integer) 
A racing track is built around an elliptical ground whose equation is given by \[ 9x^2 + 16y^2 = 144 \] The width of the track is \(3\) m as shown. Based on the given information answer the following: 
(i) Express \(y\) as a function of \(x\) from the given equation of ellipse.
(ii) Integrate the function obtained in (i) with respect to \(x\).
(iii)(a) Find the area of the region enclosed within the elliptical ground excluding the track using integration.
OR
(iii)(b) Write the coordinates of the points \(P\) and \(Q\) where the outer edge of the track cuts \(x\)-axis and \(y\)-axis in first quadrant and find the area of triangle formed by points \(P,O,Q\).