4. Which alkyl halide would be most reactive in an SN1 reaction? Explain your answer. I Br IV Br Br Br II III Give detailed Solution with explanation needed..don't give Handwritten answer Br V
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- Does ether cleavage following SN1 or SN2 ? Give your explanation.Please answer the attached question. Give the major products for the appropriate SN1 and E1 reactions and please explain how you calculated your answers. Thanks.12c. If you could, please provide an explaination for why the major product would be the SN2 product rather than E2 product?
- The following compound readily eliminates CO; to form a conjugated six membered ring. (a) Complete the reaction with drawing the possible structure and (b) explain why this reaction goes steadily.what is the order of reactivity by ranking from most to least reactive in SN2 reactions?For SN1 Explain if 3o ( tertiary) alkyl halides reacted (fastest or slowest) explain why. Be sure to explain if alkyl halides did not react or did react and why. 3o (tertiary) compounds listed are: 2-chloro-2-methylpropane (see picture) Base your explanations on the following considerations: the nature of leaving group, the effect of structure, steric hindrance and any other feature.
- Please complete both subpart reactions in clear handwritten answer on a paper!How do you properly write an SN1 reaction, with transition states/intermediate steps included?Explain how and why rearrangements occurduring Friedel-Crafts alkylation reactions formingmore than 1 product. Also illustrate therearrangement reaction from the aboveexample.