Complete the following synthesis using the shown starting material as the only source of carbon atoms...
Using propyne (structure shown) as your only source of carbon atoms, design a synthesis of the target molecule. You may use any organic or inorganic reagents you choose, but all the carbon atoms in the target must have come from propyne originally. Show the product of each step and the reagents needed for each step. Assume you have an unlimited supply of propyne.
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
Using the given aldehyde as your only source of carbon atoms,
design a synthesis pathway to generate the target.
12. (8 points) Using the given aldehyde as your only source of e given aldehyde as your only source of carbon atoms, design a synthesis pathway to generate the target. This can be done in four sys are encouraged to use a protecting group in this synthesis. o DH HO a. You must show Retrosynthetic Analysis for full credit. b. You...
Synthesis with 10 steps or less
Synthesis Problem Show all the steps required, including intermediates, for the synthesis of the following target compound, using any starting material with six (6) carbons or less, plus any other organic or inorganic reagents necessary. Determine the IUPAC systematic chemical name for your target compound. Try for io sieps or tesvs
Synthesis Problem Show all the steps required, including intermediates, for the synthesis of the following target compound, using any starting material with six...
2. Starting with ethanol as the only source of organic material and using any other reagents that you desire, write equations to show the synthesis of (a) ethanoic acid, and (b) ethyl ethanoate. (4 marks)
Provide a stepwise synthesis for the following compound using
benzyl alcohol as you only source of carbon & using any other
reagents necessary
OH
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).
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.
7) Provide a stepwise synthesis for the following compound using benzyl alcohol as your only source of carbon and using any other reagents necessary. OH OH benzyl alcohol
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...