2. Propose a synthesis for the following molecules – should not take more than 5-6 steps. Hint: they all involve a pericyclic reaction at one point. ? CI
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- How would you synthesize the followingcompounds from benzene using thereagents from the table? Each requires 3-4steps.How would you synthesize compound B from compound A? Be specific with all the reactives and solvents that are needed and also with the order of the steps to follow.Which halide in the attached marine natural product reacts fastest inthe SN2 reaction?
- p. please don't provide handwrriten solution Write the mechanism of the reaction with proper arrow formalisim, do not combine into one stepShow how m-dibromobenzene can be synthesized from benzene from multiple reactions. Tip: think of diazotation as an important reaction in this process.a,b-Unsaturated carbonyl compounds are susceptible to either 1,2 addition or 1,4 (Michael)addition. Give examples of nucleophiles that would favor each case and explain yourreasoning
- 1.Draw the product, please shows step by step in details 2.Explain if (CH3)2CH in this reaction can attach in ortho positon in Friedel Craft Alkylation?? why or why not???3) Explain how and why the reaction below results in the observed regiochemistryand/or stereochemistry.Which alkene on ozonolysis produce Pentan-3-one and 2-Methylpropanal?
- what is a possible mechanism for the following reaction ??Ochem help with reactions... See the attached image... what would be the major product(s) of the following reactions? ThanksI'm stuck on the last part, what happens after acylation since we don't have any of the reagents to leave, and NH2 is not one of course. what is D? explain please