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. ли Η
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- Using cyclooctyne as your starting material, show how you would synthesize the following compounds. (Once you haveshown how to synthesize a compound, you may use it as the starting material in any later parts of this problem.) cyclooctanoneShow 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.(a) hex-1-yne (b) hex-2-yneShow how you would synthesize the following compound using 4-methylhex-1-ene starting material and any reactions we have talked about in this course.
- 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. ) hex-3-yneStarting 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-eneWrite the products of the following sequences of reactions. Refer to your reaction roadmaps to see how the combined reactions allow you to navigate between the different functional groups. Note that you will need your old Chapters 611, Chapters 1518, and Chapter 19 roadmaps along with your new Chapters 2021 roadmaps for these.
- Write the products of the following sequences of reactions. Refer to your reaction roadmaps to see how the combined reactions allow you to navigate between the different functional groups. Note that you will need both your old Chapters 611 roadmap and your new Chapter 15 roadmap for these.Write the products of the following sequences of reactions. Refer to your reaction roadmaps to see how the combined reactions allow you to navigate between the different functional groups. Note that you will need your old Chapters 611, Chapters 1518, and Chapter 19 roadmaps along with your new Chapter 20 reaction roadmap for these.Using your reaction roadmap as a guide, show how to convert 3-hexyne into propanal. All of the carbon atoms of the target molecule must be derived from the starting material as efficiently as possible. Show all intermediate molecules synthesized along the way.
- Using hex-1-ene as your starting material, show how you would synthesize the following compounds. (Once you haveshown how to synthesize a compound, you may use it as the starting material in any later parts of this problem.) c) 2,2-dibromohexaneUsing cyclooctyne as your starting material, show how you would synthesize the following compounds. (Once you haveshown how to synthesize a compound, you may use it as the starting material in any later parts of this problem.) ) cyclooctaneShow how you would synthesize the following compounds, starting with acetylene and any compounds containing nomore than four carbon atoms. pentanal, CH3CH2CH2CH2CHO