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.

Arrange the following compounds in increasing order of their boiling points:

The reaction 
suggests that phenol is :
In the reaction R–OH + HCl $\xrightarrow{\text{ZnCl}_2}$ RCl + H$_2$O, what is the correct order of reactivity of alcohols?

A ladder of fixed length \( h \) is to be placed along the wall such that it is free to move along the height of the wall.
Based upon the above information, answer the following questions:
(iii) (b) If the foot of the ladder, whose length is 5 m, is being pulled towards the wall such that the rate of decrease of distance \( y \) is \( 2 \, \text{m/s} \), then at what rate is the height on the wall \( x \) increasing when the foot of the ladder is 3 m away from the wall?
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.