Explain why the halogens, when attached to a benzene ring, weakly deactivate the ring toward electrophilic aromatic substitution yet they are still ortho/para directors.
Q: Draw the structure of methoxybenzene and explain which product will be formed as a result of the…
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Q: Identify the ring which is more reactive towards electrophilic aromatic substitution.
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- Highlight each of the positions on the benzene ring that you expect will be most likely to react by electrophilic aromatic substitution. Am I correct?From 1 being the slowest and 4 being the fastest rank the aromatic hydrocarbons in terms of increasing raters of nitration via electrophilic aromatic substitutionSome of the groups pre-bonded to an aromatic ring cause electrophilic aromatic substitution to occur mainly at the ortho and para sites. Others lead to the meta location. Is that true or false?
- (a) For which aromatic compound do you expect nitration to take place faster: furan or thiophene? (b) For each of these compounds, at which C atom do you expectelectrophilic aromatic substitution to predominantly takeplace? Explain your reasoning.Which one would be most reactive toward electrophilic aromatic substitution?Complete the electrophilic aromatic substitution mechanisms with the necessary substances!
- Which sequence ranks the following aromatic rings of this compound in order of increasing reactivity in an electrophilic aromatic substitutionreaction (slowest to fastest reacting)?Predict the most likely sites of electrophilic aromatic substitution in each of the following molecules.Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. What is the purpose of deprotonation in the last step of electrophilic aromatic substitution? A) To neutralize the base that is present B) To make room for the electrophile C) To make the ring more reactive D) To restore an aromatic system E) None of the above
- What is the slow (rate-determining) step in any electrophilic aromatic substitution reaction? Please provide a detailed explanation.In electrophilic aromatic substitution, a group attached to the aromatic ring does not affect ring reactivity. Is that true or false?From a Nucleophilic aromatic substitution (SNA), analyze 2 possible disonnections and conclude which bond is convenient disconnect. Taking into consideration the above, suggest a retro-synthesis and a synthesis for the following molecule. (Lobenzarit)