1) Propose a synthesis of the following amine from ethanol. Ethanol should be the only carbon source you use. 2) Propose a synthesis. 3) Propose a synthesis. 1) PCC pn. 3)acid work up 5) 03 6) DMS 7)? 8)? 9) H/Ni 4) Propose a synthesis. 5) Name the following using IUPAC nomenclature.
Propose a synthesis. Intermediate is appreciate
3) Propose a synthesis. T ph 1) PCC OH NH 2) 3)acid work up 4) ? 5) 03, 6) DMS 7)? 8)? 9) H/Ni
3) Propose a synthesis. 1) PCC 3)acid work up 4) ? 5) 03, 6) DMS 7)? 8)? 9) H/Ni
Problem 5: Propose a synthesis that would convert the starting material to the desired product. Problem 6: Propose a synthesis that would convert the starting material to the desired product. OH
Problem 6 (10 pts) Propose a synthesis of the molecule shown below from cyclohexanol and 1-butanol using any other reactions necessary to prepare intermediates O.
Problem 6 In the synthesis of lansoprazole, 2,3-dimethylpyridine is converted to the compound shown. Propose a synthesis CF3
propose a synthesis of halomon from 2-butene
Propose a multistep synthesis of phenylacetaldehyde from benzene
please explain
Problem 5 (10 pts) Starting from acetylene propose a synthesis of both cis-3-heptene and trans-3-heptene.
Problem 3 Propose a synthesis of the following molecule from the given starting material. You may use any reactions we have learned in this course so far, and any reagents containing the carbon atoms you need. If you make a mixture in any of the steps, place a box around the compound you would separate from the mixture, and carry on with your synthesis assuming you can isolate the desired regioisomer. NH2