Design a synthesis of each of the following target molecules starting from methylcyclohexene and any noncyclic...
Design a multi-step synthesis for each of the following target molecules from the indicated starting material. Show the reagents needed for each step and the product of each step. Do not show any mechanisms. Draw the structures of the diene and the dienophile that reacted to form the Diels-Alder product shown. Provide the missing reagents in this multistep synthesis.
Design a synthesis of the target from the starting material and any other reactants and reagents. 4) Br
#19 all 6 synthesis Design a synthesis of each target using the starting material and any reagents containing three carbons or less. Read the assigned pages in the text, and do the assigned problems
a synthesis of each of the following target molecules from the starting reagent synt (8) 4. Sh ow methylenecyclohexane Br CH2 CH3 ?? Br ?? ??
Design an efficient synthesis for the following target molecule, using any hydrocarbons with three or less carbon atoms as starting materials to build the target molecule; also using any solvents or reagents that do not contribute carbon atoms to the final structure. SHOW YOUR ANSWER AS A STEPWISE REACTION SCHEME SHOWING THE REAGENT REQUIRED AND PRODUCT OF EACH STEP DO NOT SHOW MECHANISMS (i.e. curly arrows are NOT required) Any solvents or reagents that do not contribute carbon atoms to...
Use retrosynthesis to design a synthesis of each target using the starting material and any reagents containing three carbons or less. 5. Target Starting Material Target Starting Material OH COH H C Dis Explain why an electron pair in an sp hybrid orbital is lower in potential energy than an electron pair in an sp hybrid 6. H orbital. Explain why ethy ne is more acidic than 7 ethene or ethane. H-CRCE pk, s0 Construct an explanation for why the...
Starting from Benzene and using reagents that we have discussed in class, design a synthesis for the Target molecule (TM). TM SM
3. Design a synthesis of the following molecule starting from benzene and molecules of two or less carbon atoms. You are not limited in your choice of reagents or number of steps. ΝΟ2 ΝΗ2 12 Br 10 Cl CO2H он CI ΝΟ2 ΝΗ2 12 Br 10 Cl CO2H он CI
For 1 - 3, design reasonable syntheses of each of the target molecules using the provided starting material and organic and inorganic reagents of your choice. Show the reagents needed for each step and the product of each step. Do not show any mechanisms. Please put all your answers on this sheet. Write your answers like this (actual number of starting steps may vary)material reagent(s) reagent(s) ABCD target Two equally reasonable routes are possible Can you find them both? (For...
Design an effective synthesis for each of the following amino acids starting from the compounds shown on the left. You may also use any monofunctional organic compound containing four or less carbon atoms, and any inorganic reagents in your syntheses.