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Multistep Synthesis (9 pts) Show how to convert benzene into at least one of the molecules...
21. Do Only One! Propose a multistep synthesis using the starting materials shown and any other...
21. Do Only One! Propose a multistep synthesis using the starting materials shown and any other reagents/reactants you need. To maximize partial credit, be sure to draw out the products of each reaction you propose. You do not need to draw mechanisms for full credit. (7 points) o by OR ОMe
Show how you would accomplish the following synthesis, in good overall yield, using the indicated starting...
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...
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...
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...
synthesis show how the immune could be prepared from benzene propanoic acid and dimethylamine. More than...
synthesis show how the immune could be prepared from benzene
propanoic acid and dimethylamine. More than one synthetic
transformation will be necessary
give all possible structures of the product C 10 H 1203 form
by intermolecular placing condensation of the keto Ester shown
below
ps * Bookmarks Gmail YouTube Maps Ch15: Oxidation o. 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...
7. Synthesis Problem (15 points) Show how you would synthesize 3 of the 4 following compounds...
7. Synthesis Problem (15 points) Show how you would synthesize 3 of the 4 following compounds in one chemical reaction. You may use any starting material you wish and any organic and inorganic reagents. Clearly indicate which ones you want graded by circling the molecules н, осн, Br ОН
5. Synthesis: Show how the amine could be prepared from benzene, propanoic acid and dimethyl amine....
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. Он and and 6. Give all possible structures of the product (C20H1203) formed by intramolecular Claisen condensation of the keto-ester shown below. 1. NaOH 2. H30 Page 3 of 4
using the reagents listed below, propose a synthesis of the target compound starting from benzene. Remaining...
using the reagents listed below, propose a synthesis of the
target compound starting from benzene.
Remaining Time 58 minutes, 36 send Question Completion Status Using the registed below, propone a thesis of the target compound starting from benzene. Enter your awwer as a lof letters corresponding to the selected register you wish to use them You may assume that all reactions appropriately worked up and that matures of construtorallomers can be separed. You may use a reagent more than one...
Proposed Synthesis Show the structure of your target molecule as well as synthetic schemes illustrating the two st...
Proposed Synthesis Show the structure of your target molecule as well as synthetic schemes illustrating the two steps required for preparing it from "allowed" starting materials. For each synthetic step indicate the source of the experimental procedure you will follow-sources can either be literature references or simply the course pack itself. (See the example below for the format to be followed) ~Example Target Molecule: NO2 Cl Step 1: OH Reference: Tetrahedron, 1990, 46, 2975 HNO3 Step 2 o H2SO4 NO2...
How would you convert an unsaturated fatty acid into a saturated fatty acid A. KMnO4, "OH,...
How would you convert an unsaturated fatty acid into a saturated fatty acid A. KMnO4, "OH, heat B. "OH,H,O, heat; then H,0 C. Hz, Ni, pressure D. H,0,H,O, heat 26. What structure has the following proton NMR spectrum? 'H NMR: doublet, 6.6 ppm, 2H doublet, 7.8 ppm, 2H broad singlet, 4.2 ppm, 2H singlet, 2.1 ppm, 3H HUN 27. Which of the following is the correct synthesis of the compound shown? CH, Br o Na Na o CH,Br B. T...
21. Do Only One! Propose a multistep synthesis using the starting materials shown and any other reagents/reactants you need. To maximize partial credit, be sure to draw out the products of each reaction you propose. You do not need to draw mechanisms for full credit. (7 points) o by OR ОMe
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...
synthesis show how the immune could be prepared from benzene
propanoic acid and dimethylamine. More than one synthetic
transformation will be necessary
give all possible structures of the product C 10 H 1203 form
by intermolecular placing condensation of the keto Ester shown
below
ps * Bookmarks Gmail YouTube Maps Ch15: Oxidation o. 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...
7. Synthesis Problem (15 points) Show how you would synthesize 3 of the 4 following compounds in one chemical reaction. You may use any starting material you wish and any organic and inorganic reagents. Clearly indicate which ones you want graded by circling the molecules н, осн, Br ОН
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. Он and and 6. Give all possible structures of the product (C20H1203) formed by intramolecular Claisen condensation of the keto-ester shown below. 1. NaOH 2. H30 Page 3 of 4
using the reagents listed below, propose a synthesis of the
target compound starting from benzene.
Remaining Time 58 minutes, 36 send Question Completion Status Using the registed below, propone a thesis of the target compound starting from benzene. Enter your awwer as a lof letters corresponding to the selected register you wish to use them You may assume that all reactions appropriately worked up and that matures of construtorallomers can be separed. You may use a reagent more than one...
Proposed Synthesis Show the structure of your target molecule as well as synthetic schemes illustrating the two steps required for preparing it from "allowed" starting materials. For each synthetic step indicate the source of the experimental procedure you will follow-sources can either be literature references or simply the course pack itself. (See the example below for the format to be followed) ~Example Target Molecule: NO2 Cl Step 1: OH Reference: Tetrahedron, 1990, 46, 2975 HNO3 Step 2 o H2SO4 NO2...
How would you convert an unsaturated fatty acid into a saturated fatty acid A. KMnO4, "OH, heat B. "OH,H,O, heat; then H,0 C. Hz, Ni, pressure D. H,0,H,O, heat 26. What structure has the following proton NMR spectrum? 'H NMR: doublet, 6.6 ppm, 2H doublet, 7.8 ppm, 2H broad singlet, 4.2 ppm, 2H singlet, 2.1 ppm, 3H HUN 27. Which of the following is the correct synthesis of the compound shown? CH, Br o Na Na o CH,Br B. T...
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