Page 2 of 2 ZOOM Show how you would accomplish the following synthesis in good yield....
3. Show how you would add a Grignard reagent to an acid chloride to synthesize 4-phenylheptan-4-01 4. Show how you would accomplish the following synthesis in good yield. OH benzoic acid N.N-dimethylbenzamide NH HO hexanol heptane-1-amine 0 0 methyl 2-phenylacetate 3-phenylpropionitrile но-л-он
10% Multi Step Reactions 6) Show how you would accomplish the following synthesis in good yields. You may use any reagents that you wish. Hint: Protect 2 different functional groups if you choose to use a Grignard's reagent. :OH : OH но 10% Multi Step Reactions 6) Show how you would accomplish the following synthesis in good yields. You may use any reagents that you wish. Hint: Protect 2 different functional groups if you choose to use a Grignard's reagent....
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...
2) Show how you would accomplish the following transformations. These are all essentially one step reactions (depending on how you count). OH Br OH OH OH он OH он 0 но
Show how you would synthesize the following 3- amine in good yield using alcohols of carbons 4 or less as your only source of carbon CH3 、CH3
Choose the correct reagents for each step to accomplish the following synthesis in good chemical yield. Write the letter from each box in the spaces below. Choose the correct reagents for each step to accomplish the following synthesis in good chemical yield Write the letter from each box in the spaces below CH3 Rxn 1 Rxn 2 02 Rxn 3 Rxn 4 a. NBS, hv b. HBr c. Br2, FeBr3 AICl3 AlCI3 i. HCI, Zn(Hg) CH2N2 then H3O* Rxn 1...
(IPJ Snow how would you accomplish the following synthesis in good vield. Indicate all the reagents you need draw the structures that result after each step in your synthesis. Nr.
1. Give a sequence of reactions to accomplish the following transformation? Show mechanism 2. What reagent(s) would accomplish the following? Show mechanism. R-CH2-NH2 R-C-NH2 3. What would result from the reactions shown below? Hsco-s-OCH3 large excess) NaOH нон H,0 но ОН "ОН (a and B) 4. Predict the major product of the following reaction. CHNNH 3 equivalents) но CHCH2OH Heat он CH2OH Draw the Haworth projection for chair conformation of a-D-Glucopyranose (shown below) CH2OH HO H OH OH