Get the answers you need at Westonci.ca, where our expert community is always ready to help with accurate information. Our platform offers a seamless experience for finding reliable answers from a network of experienced professionals. Get precise and detailed answers to your questions from a knowledgeable community of experts on our Q&A platform.
Sagot :
Answer:
3 > 2> 1
Explanation:
Aromatic compounds undergo electrophilic substitution reaction which passes through a positively charged intermediate to yield the product.
Substituted benzenes may be more or less reactive towards electrophilic aromatic substitution than benzene molecule depending on the nature of the substituent.
Certain substituents increase the ease of reaction of benzene towards aromatic substitution.
If we look at the compounds closely, we will notice that toluene reacts readily with CH3Cl / AlCl3. This is because, the methyl group is electron donating hence it stabilizes the positively charged intermediate produced in the reaction.
Carbonyl compounds are electron withdrawing substituents hence they decrease the magnitude of the positive charge and hence decrease the rate of electrophilic aromatic substitution.
Thank you for your visit. We're dedicated to helping you find the information you need, whenever you need it. Your visit means a lot to us. Don't hesitate to return for more reliable answers to any questions you may have. Stay curious and keep coming back to Westonci.ca for answers to all your burning questions.