Show work and label reactions. Starting from benzonitrile and ethanol as your only sources of carbon...
please help me to sythesize this from benzonitrile and ethanol as your only sources of carbon in the final molecule, syr the following using any reagents. NH2 OHTO zncaract A MOTH Starting from toluene and ethanol as your only sources of carbon in the final molecule, sy following
Show work and solve Starting from toluene and ethanol as your only sources of carbon in the final molecule, synthesize the following
Synthesize the compounds shown below utilizing only the carbon sources provided and any reagents of your choosing. Target Molecules Carbon Sources H3C OH OH 了」 。 Hsc
From propane as the only starting carbon source, synthesize 3-propoxyhexane. (please show synthesis of any organic reagents which appear in the final product)
Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent....
Show your steps and reaction conditions clearly. No reaction mechanisms are required. (a) Using acetone and 2.2-dimethylpropanal as your only sources of carbon atoms, show how you would synthesize compound 1. Hint: Reaction of a diol and a carbonyl compound. Starting from 1-ethoxynaphthalene and 3-methylbutanoic acid as your only sources of carbon atoms, show how you would synthesize the ester 1. Hint oxidation of a ketone to ester (C) Suggest a synthesis for compound 1 using as starting materials/reactants benzaldehye....
Synthesize the target molecule (the one at the top) from each of the two starting materials (each starting material is a separate synthesis). Any additional sources of structural carbons can only have 1 C atom at a time. но. он ОН NH о
8. Synthesis: Using the starting materials below as your only carbon sources, synthesize the desired product (hint: you will have to use the ester multiple times!)
You have toluene, methanol, ethanol, and propanol as C (Carbon) sources and any solvents or reagents necessary to do your synthesis. You must include solvents and reagents for each step and make sure that all C's (Carbons) in your target molecule come from the available alcohols. The target molecule is 3-benzyl-2,3-pentanediol
Propose a synthesis of the following amine from ethanol. Ethanol should be the only carbon source you use. Means every carbon in the product should come from an ethanol. You can use ethanol multiple times to get the reagents you need. You can combine the intermediates you obtain from ethanol to get the final product. 4) Propose a synthesis. Ե Ե -NH I Ե Ե Ե Ե 5) Propose a synthesis T Ե Ե