Highlight each of the positions on the benzene ring that you expect will be most likely to react by electrophilic aromatic substitution. Br CN ☑
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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. CH,O. H XHighlight each of the positions on the benzene ring that you expect will be most likely to react by electrophilic aromatic substitution. ☑ .SO₂H CH3 ☑For each of the molecules below, highlight each of the positions on the benzene ring that you expect will be most reactive towards electrophilic aromatic substitution. HN & bo HO X
- Usually at the 2- or 3- position, Thiophene undergoes electrophilic aromatic substitution. Draw the intermediates and all resonance structures for the reaction at each position, and then decide what position should be more reactive depending on your intermediates.The compound below can be prepared with an alkyl iodide and a suitable nucleophile. Identify the alkyl iodide and the nucleophile that you would use. For an anionic nucleophile, you do not need to draw the counterion. Alkyl iodide: OH Draw Your Solution Nucleophile: Draw Your Solution SUPPORT6) Develop a series of reactions we have covered in lecture that would produce the following molecules. Use any reagents necessary, but you must start with an alkene with one double bond (any alkene you choose) as one of your reactants. он
- 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?What are the relative rates of the following nucleophilic substitution reaction below.Explain why quinuclidine is a much more reactive nucleophile thantriethylamine, even though both compounds have N atoms surroundedby three R groups.
- 9. On each of the structures shown below mark with an arrow where electrophilic aromatic substitution would take place. CN SO3H OH NO₂Explain why quinuclidine is a much more reactive nucleophile than triethylamine, even though both compounds have N atoms surrounded by three R groups.Chemistry Please help explain this textbook question: Although N, N -dimethylaniline is extremely reactive toward electrophilic aromatic substitution and is readily substituted by weak electrophiles, such as diazonium and nitronium ions, this reactivity is greatly diminished by the introduction of an alkyl substituent in an ortho position.