1) Using 3-methyl-1-butene as the only source of carbon, and any other reagents, outline a synthesis...
Outline a synthesis of the following compound from the compound below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. Ignore E/Z stereoisomers for the product alkene. from as the only source of carbon Outline a synthesis of the following compound from the compound below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. Ignore E/Z stereoisomers for the product alkene. from as the only source...
Starting with nitrobenzene and using any other reagents of your choice, outline a synthesis of para-chloroaniline Using acetic acid as your only source of carbon atoms, show how could you make N-ethylacetamide:
using basic reactions and grignard. Outline a synthesis of the following compound from the compounds below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. 2 OH , CH3 CH3 from 2 OH CH CH3 Outline a synthesis of the following compound from the compounds below as the only source of carbon incorporated into the final product, and any needed inorganic reagents. 2 OH , CH3 CH3 from 2 OH CH CH3
Name 4. Starting with cyclohexene and acetylene as the only source of carbons, show a synthesis of the compound below. 1. Show how you could make the given product from the given starting material. Show all steps. OH a CECH 2. Starting with acetylene and methyl bromide as your only source of carbons show a synthesis of cis-2-butene. 5. Prepare 2-methoxy-propanol from 1-bromo-propane. Show the steps and use any reagents you need. 3. Using acetylene and propyl bromide as your...
3. Synthesize the following alcohol using ethyne as the only source of carbon atoms. Any other reagents needed may be used. You can use as many molecules of ethyne as necessary H-CEC-H HO ethyne target alcohol 3. Synthesize the following alcohol using ethyne as the only source of carbon atoms. Any other reagents needed may be used. You can use as many molecules of ethyne as necessary H-CEC-H HO ethyne target alcohol
Devise a synthesis for the compound below using cyclopentane as your only source of carbon. You may use any other reagents. The most efficient route includes a Diels-Alder reaction, two radical halogenation reactions and two elimination reactions.
Starting with propane as the only source of carbon and using only other INORGANIC reagents provide a step- by- step synthesis of cis-hex-2-ene. Assume isomers can be separated (be regio- and stereo- specific).
Starting from methyl acetoacetate and any other necessary reagents, complete the most efficient threestep synthesis of the ketone, 3-benzyl-5-methylhexan-2-one, by dragging the appropiate compound(s) into the boxes. Only one set of reagents will fit into each box, and all compounds will not be used.
Using a Gilman reagent as the key step, outline a synthesis of the following compound from ethyne as the only source of carbon for the main 4-carbon chain and any needed inorganic reagents (the -CN comes from inorganic NaCN).
Propose a stepwise synthesis for N-propylbutanamide. using 1-proanol and/or carbon dioxide as your only source of carbon and using any other reagents necessary. Detail how the final product could be identified using a spectroscopic method.