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.

(N/A) $(i)$ 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 structures.
Thus,the benzene ring 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 electrophilic substituents are directed to the ortho and para positions in the benzene ring.