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.
Write the IUPAC name of the product formed in the Reimer-Tiemann reaction.
A certain reaction is 50 complete in 20 minutes at 300 K and the same reaction is 50 complete in 5 minutes at 350 K. Calculate the activation energy if it is a first order reaction. Given: \[ R = 8.314 \, \text{J K}^{-1} \, \text{mol}^{-1}, \quad \log 4 = 0.602 \]
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.