Homework Answers
b) i. Reaction of sodamide
with 1,2-dibromo compound will give us alkyne as a product.
ii. Alkyne on reaction with strong base like sodamide following by SNr reaction with benzylbromide we will end up with our desired product.
c) Reaction of acetyl group will sodamide followed by epoxide we will get trans alcohol.
ii. By protection of alcohol with Tosylchloride and attack of cynide will give us cis compound as a our desired product.
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b) Show how you would accomplish this synthesis. You may use any reactants/reagents. thermo Only your...
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...
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....
8. Show how you would accomplish the following syntheses. You may use whatever additional reagents you...
8. Show how you would accomplish the following syntheses. You may use whatever additional reagents you need. The synthesis should not take more than three or four reactions. At least one of the reactions should come from the aldehydes and ketones chapter. (6 pts) a) CO2H b)
Show how you would accomplish the following synthetic conversion starting with ethanol as the only source...
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....
20% Multi-Step Synthesis Sa) Show how you could perform the following synthesis. You may use any reagents that you need. 20% Multi-Step Synthesis Sa) Show how you could perform the following...
20% Multi-Step Synthesis Sa) Show how you could perform the following synthesis. You may use any reagents that you need.
20% Multi-Step Synthesis Sa) Show how you could perform the following synthesis. You may use any reagents that you need.
Using any of the reagents drawn below as the only sources of the carbons in your...
Using any of the reagents drawn below as the only sources of the carbons in your target molecule, propose a multistep synthesis for the molecule drawn in the box below. Show all reagents and intermediate products that are formed in each step of the way. (8 pts) Reagents - Only Source of Carbons corocco tante como Target Molecule Using any of the reagents drawn below as the only sources of the carbons in your target molecule, propose a multistep synthesis...
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI. Devise a synthesis that will accomplish the following transformati...
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI. Devise a synthesis that will accomplish the following transformation in good yield. Use the given compounds as the only organic source of carbon atoms. You may use any common organic solvents as well as any needed inorganic reagents
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI....
organic chemistry: show how you would accomplish the following multi-step synthesis using the indicated starting material...
organic chemistry:
show how you would accomplish the following multi-step
synthesis using the indicated starting material and any necessary
reagents
hept-b-en-1-al E - caprolactone
Show how you would accomplish the following syntheses. You may use whatever additional reagents you need....
Show how you would accomplish the following syntheses. You may use whatever additional reagents you need. HO?,CH, CHO CH,OH CHO CHO H OH CH2Br Ph (d) CH, CH CH CH CH,-C-Ph (f) BrCH,CH,CCH, HC=CCH,CH-CCH, ->
Select reagents from the table to show how you would carry out this synthesis. (Enter your...
Select reagents from the table to show how you would carry out
this synthesis. (Enter your answer as a series of letters, i.e.
jbc, in the order that you wish to use the reagents. Repeat a
letter if you want to use more than one equivalent of the reagent.
Do not use commas or spaces.)
H3C CH2 H3C Select reagents from the table to show how you would carry out this synthesis. Reagents Available a: Br2, CH2Cl2 f. Li, NH3...
Problem #2 Show how you would accomplish the following transformation. You may use any reagent necessary....
Problem #2 Show how you would accomplish the following transformation. You may use any reagent necessary. Oh oh
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....
8. Show how you would accomplish the following syntheses. You may use whatever additional reagents you need. The synthesis should not take more than three or four reactions. At least one of the reactions should come from the aldehydes and ketones chapter. (6 pts) a) CO2H b)
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....
20% Multi-Step Synthesis Sa) Show how you could perform the following synthesis. You may use any reagents that you need.
20% Multi-Step Synthesis Sa) Show how you could perform the following synthesis. You may use any reagents that you need.
Using any of the reagents drawn below as the only sources of the carbons in your target molecule, propose a multistep synthesis for the molecule drawn in the box below. Show all reagents and intermediate products that are formed in each step of the way. (8 pts) Reagents - Only Source of Carbons corocco tante como Target Molecule Using any of the reagents drawn below as the only sources of the carbons in your target molecule, propose a multistep synthesis...
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI. Devise a synthesis that will accomplish the following transformation in good yield. Use the given compounds as the only organic source of carbon atoms. You may use any common organic solvents as well as any needed inorganic reagents
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI....
organic chemistry:
show how you would accomplish the following multi-step
synthesis using the indicated starting material and any necessary
reagents
hept-b-en-1-al E - caprolactone
Show how you would accomplish the following syntheses. You may use whatever additional reagents you need. HO?,CH, CHO CH,OH CHO CHO H OH CH2Br Ph (d) CH, CH CH CH CH,-C-Ph (f) BrCH,CH,CCH, HC=CCH,CH-CCH, ->
Select reagents from the table to show how you would carry out
this synthesis. (Enter your answer as a series of letters, i.e.
jbc, in the order that you wish to use the reagents. Repeat a
letter if you want to use more than one equivalent of the reagent.
Do not use commas or spaces.)
H3C CH2 H3C Select reagents from the table to show how you would carry out this synthesis. Reagents Available a: Br2, CH2Cl2 f. Li, NH3...
Problem #2 Show how you would accomplish the following transformation. You may use any reagent necessary. Oh oh
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