?? Starting with acetylene, any halide 4C), and any other reagents required, make the target molecule....
. Starting with acetylene, any halide ($4C), and any other reagents required, synthesize the target molecule. (8 pts) TM Starting with acetylene, any halide (S4C), and any other reagents required, synthesize the target molecule. (7 pts) 2. OH TM
Provide retrosynthetic analysis and synthesize the following molecule from acetylene and an alkyl halide. 3. Provide retrosynthetic analysis and synthesize the following molecule from acetylene and an alkyl halide: OH
Propose a synthesis using the target molecule with retrosynthetic analysis. Provide complete reagents for each step of your proposed synthesis. from Target molecule from Target molecule
13. Using acetylene as one of the starting materials and any other reagents required, outline a synthetic route (including all reagents, proper order of addition and the product for each step) to obtain the following compound (with the stereochemistry shown):
14. Starting with an appropriate alkyl halide and using any other needed reagents, outline the syntheses of each of the following. When alternative possibilities exist for a synthesis, you should choose the one that gives the better product. Indicate whether each reaction follows an SN1 or SN2 reaction mechanism. 14. Starting with an appropriate alkyl halide and using any other needed reagents, outline the syntheses of each of the following. When alternative possibilities exist for a synthesis, you should choose...
using any reagents show retrosynthetic analysis and then show entire synthesis in forward sense SIcP f youl proposed syninesis. from Target molecule SIcP f youl proposed syninesis. from Target molecule
VI. Starting from acetylene (CH C H) and using any needed reagents to synthesize the following molecule: Show every single step of the synthesis (10 pts)
Design a synthesis of the target from the starting material and any other reactants and reagents. 4) Br
Demonstrate a retrosynthetic analysis (disconnection approach) to make the target molecule. You may invoke any reagent in your synthesis but are restricted to nitrobenzene and methane as carbon sources that end up in your product. OH
Starting with acetylene use a sequence of reagents to show how you could make each of the following products. Note that some steps will be redundant so please just start from a common intermediate once you have shown its synthesis. For example, all of the other products can be made from either 1-butyne or 2-hexyne. You may not use any other source of C other than methyl bromide, calcium carbide, chloroform and the products you can make from these sources....