Explain the fact that in aryl alkyl ethers
(i)the alkoxy group activates the benzene ring towards electrophilic substitution and
(ii)it directs the incoming substituents to ortho and para positions in the benzene ring.
(i)In aryl alkyl ethers, due to the +R effect of the alkoxy group, the electron density in the benzene ring increases as shown in the following resonance structure. Thus, benzene is activated towards electrophilic substitution by the alkoxy group.
(ii)It can also be observed from the resonance structures that the electron density increases more at the ortho and para positions than at the meta position. As a result, the incoming substituents are directed to the ortho and para positions in the benzene ring.


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 \(P,O,Q\).
Alcohols, phenols, and ethers are organic compounds that can be classified based on their molecular structure and functional groups.
Classification of Alcohols:
Classification of Phenols:
Classification of Ethers:
In summary, alcohols, phenols, and ethers can be classified based on their molecular structure and functional groups. Understanding the classification of these compounds is important for predicting their reactivity and understanding their potential applications in various fields, including chemistry, biology, and industry.