Show how you would synthesize the following compound using 2-methylhex-1-ene starting materials and any chemical reactions we have talked about in this course. H
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- Wittig reactions with the following -chloroethers can be used for the synthesis of aldehydes and ketones. (a) Draw the structure of the triphenylphosphonium salt and Wittig reagent formed from each chloroether. (b) Draw the structural formula of the product formed by treating each Wittig reagent with cyclopentanone. Note that the functional group is an enol ether or, alternatively, a vinyl ether. (c) Draw the structural formula of the product formed on acid-catalyzed hydrolysis of each enol ether from part (b).Muscalure is the sex attractant of the common housefly. Flies are lured to traps filled with bait thatcontain muscalure and an insecticide. Eating the bait is fatal. How could you synthesize muscalure using 1-bromopentane as one of the starting materials?Starting from bromobenzene and any other reagents and solvents you need, show how you would synthesize the followingcompounds. Any of these products may be used as starting materials in subsequent parts of this problem. 2-phenylbut-2-ene
- The following reaction was performed as part of a research program sponsored by the National Institutes of Health to develop therapeutic agents for the treatment of cocaine addiction. Using what you have seen about the reactions of halogens with alkenes, propose a mechanism for this process.What will be the resulting products structure when 1-butanol is allowed to react with Jones reagent?Muscalure is the sex attractant of the common housefly. Flies are lured to traps filled with bait that contain muscalure and an insecticide. Eating the bait is fatal. How could you synthesize muscalure using 1-bromopentane as one of the starting materials?
- Please provide the reagents for the following transformations.Show how you would synthesize the following compounds from alkyl halides, vinylhalides, and aryl halides containing no more than six carbon atoms. trans-oct-3-eneWrite the products of the following sequences of reactions. Refer to your reaction roadmap to see how the combined reactions allow you to “navigate” between the different functional groups.
- Show how you might synthesize the following compounds, using acetylene and anysuitable alkyl halides as your starting materials. If the compound given cannot besynthesized by this method, explain why. 5-methylhex-2-yneShow how you would synthesize the following compounds, starting with acetylene and any compounds containing nomore than four carbon atoms. pentanal, CH3CH2CH2CH2CHO2-Butene-1-thiol is one component of skunk spray. how would you synthesize this substance from methyl-2-butenoate? from 1,3-butadiene?