Ans
5. Given the following retrosynthetic analysis, show how to synthesize the following tertiary amine as a...
וווו והו vide a retrosynthetic analysis to show how you would synthesize the following molecule. As starting erials you may use any alcohols of 5 carbons or less. You may use any necessary solvents and inorganic eagents. There is no need to show reaction mechanisms, just reactants, conditions and products (10 points). HyC
5. Show how to synthesize the following molecules using the given starting material. Show all the intermediate products for multiple steps. You can use any other reagents or starting materials necessary D amer --
Provide retrosynthetic analysis and synthesize the following
molecule from acetylene and an alkyl halide.
3. Provide retrosynthetic analysis and synthesize the following molecule from acetylene and an alkyl halide: OH
5. Synthesis: Show how the amine could be prepared from benzene, propanoic acid and dimethyl amine. More than one synthetic transformation will be necessary. You have unlimited access to any inorganic reagent. and OH and
Show how you would accomplish the following synthesis, in good overall yield, using the indicated starting materials and any other necessary reagent(s) (as long as these are involved in reactions presented/reviewed in course notes/lecture videos). State clearly all required reagents and conditions (if these are important for the outcome of the reaction). There is no need to provide mechanistic details or to show retrosynthetic analysis. (Important: please, keep in mind that submission of unnecessary content that is incorrect will be...
Show how you would accomplish the following synthesis, in good overall yield, using the indicated starting materials and any other necessary reagent(s) (as long as these are involved in reactions presented/reviewed in course notes/lecture videos). State clearly all required reagents and conditions (if these are important for the outcome of the reaction). There is no need to provide mechanistic details or to show retrosynthetic analysis. (Important: please, keep in mind that submission of unnecessary content that is incorrect will be...
Show how you would accomplish the following synthesis, in good overall yield, using the indicated starting materials and any other necessary reagent(s) (as long as these are involved in reactions presented/reviewed in course notes/lecture videos). State clearly all required reagents and conditions (if these are important for the outcome of the reaction). There is no need to provide mechanistic details or to show retrosynthetic analysis. (Important: please, keep in mind that submission of unnecessary content that is incorrect will be...
5. For the following molecule: a) perform a thorough retrosynthetic analysis, including Evans-Lapworth charge affinity analysis, for the target (and any intermediate target(s) you generate as part of your analysis) to guide your bond disconnections (28 points), and b) from your retrosynthetic analysis, propose a synthetic scheme from any reagents of three carbons or less. You can also use any reagents larger than these limits as long as only the specified number of carbons, or less, become incorporated from those...
Show how you would synthesize the following a n d beginning with 1-butene, Bromma and any necessary additional reagents. More than one step is needed. Br Bromobenzene, 1-Butene < Show how you woull Synthesize 4.- Nonanone, begining with 1-Butanol and any other non-organic reagents. (1-Butanol is the only Organic compouno available). only organ n
sbow how you woukd synthesize each of the following compounds from
benzene
(a) Show how you would synthesize each of the following compounds from benzene. Br (b) (c) (d) NHA Br. Br. (e) HN NH2