D P Highlight each of the positions on the benzene ring that you expect will be most likely to react by electrophilic aromatic substitution. N. show work. don't give Ai generated solution
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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.
N.
show work. don't
give Ai generated
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- Please answer completely will give rating surely Both questions answers neededSN2 and E2 will never have carbocations in the mechanismTherefore, this reaction cannot start with L.L.G. Explain why?Hint: InductionClick on the electrophilic center of all species that act as electrophiles in this mechanism: Acetone (CH3COCH3) OH O Targets placed: 0/3 You can place up to 3 targets O.. :OH + H₂O lib qp f : OH Undo Delete selected Remove All
- Pls help ASAP on both questions I HUMBLY REQUESTPropose a synthesis to form cyclohexyl cyclohexanoate using methylene cyclohexane as your only source of carbon. ? oso HINT: There are two cyclohexanes in the product, so this'll definitely involve splitting the starting material in half and doing two paths with it, and joining the two parts at the end...Pls help ASAP on both pls I HUMBLY request
- 4;;5) We discussed how oxygen nucleophiles can attack the carbonyl of a ketone or aldehyde, but those are not the only nucleophiles that do so! Consider the reaction below. The product of the reaction is analyzed using IR spectroscopy and there is no carbonyl signal in the IR spectrum. O HCI a) Propose a structure for the product of the reaction in the space above. b) Provide a curved arrow mechanism for the transformation.Give detailed Solution with explanation needed..give correct answer if you not then don't give answer..I will give you upvote..draw out all of the substitution and elimination reactions
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