. Starting with acetylene, any halide ($4C), and any other reagents required, synthesize the target molecule....
?? Starting with acetylene, any halide 4C), and any other reagents required, make the target molecule. C. Retrosynthetic Analysis Synthesis
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)
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
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):
13.) Provide a synthesis for the target molecule shown. (18
pts)product. (6 pts)
Bonus: (10 pts)
Starting from Benzene and using reagents that we have discussed
in class, design a synthesis for the Target molecule (TM)
13. Provide a synthesis for the target molecule shown. (18 pts) go alcohol aketone OH СОН M 얘 SM omgBr =sin 1-2 OH => KongBros Naz6.2010 H2SO4, H2O & H300 q Etmaira H20 어 #C=, 2° alcohol, aldehyde 20 TM o o #C77, Ketore...
Synthesize the following compounds from the given starting material. You may add on any alkyl/alkyl halide under 6 carbons or any necessary inorganic reagent needed (this includes triphenyl phosphine (Ph3P). Draw all intermediates and reagents necessary to reach product. OH tar
provide a synthesis for the target molecule shown.
н" TM SM Bonus: (10 pts) Starting from Benzene and using reagents that we have discussed in class, design a sy molecule (TM).
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...
Starting with acetylene and bromoethane, show how you would use reagents from the table to synthesize 3,4-epoxyhexane.
(Enter your choices as a string of letters without punctuation, i.e. ace.)
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d. Prepare octane from 1-pentyne, indicate each needed
reagents.
e. Synthesize cis-2-hexene from 1-pentyne and an alkyl
halide.
f. Synthesize trans-2-hexene from 1-pentyne and an alkyl
halide.
Synthesize each compound from acetylene. You may use any other organic or inorganic reagents. a.