What happens when
(i)n-butyl chloride is treated with alcoholic KOH
(ii)bromobenzene is treated with Mg in the presence of dry ether
(iii)chlorobenzene is subjected to hydrolysis
(iv) ethyl chloride is treated with aqueous KOH
(v)methyl bromide is treated with sodium in the presence of dry ether
(vi)methyl chloride is treated with KCN?
(i)When n−butyl chloride is treated with alcoholic KOH, the formation of but−l−ene takes place. This reaction is a dehydrohalogenation reaction.

(ii)When n−butyl chloride is treated with alcoholic KOH, the formation of but−l−ene takes place. This reaction is a dehydrohalogenation reaction.

(iii)Chlorobenzene does not undergo hydrolysis under normal conditions. However,it undergoes hydrolysis when heated in an aqueous sodium hydroxide solution at a temperature of 623 K and a pressure of 300 atm to form phenol.

(iv)When ethyl chloride is treated with aqueous KOH, it undergoes hydrolysis to form ethanol.

(v)When ethyl chloride is treated with aqueous KOH, it undergoes hydrolysis to form ethanol.

(vi)When methyl chloride is treated with KCN, it undergoes a substitution reaction to give methyl cyanide.

Give two differences between N1 and N2 reactions.
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 \(P,O,Q\).