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8. Predict the number of peaks and the 'H splitting (multiplicity) for the following compound: он...
Predict the multiplicity M (the number of peaks as a result of splitting) for each labeled...
Predict the multiplicity M (the number of peaks as a result of
splitting) for each labeled proton in the following
compound.
H H H
Synthesis with 10 steps or less Synthesis Problem Show all the steps required, including intermediates, for the synthesis of the following target compound, using any starting material with six (6) ca...
Synthesis with 10 steps or less
Synthesis Problem Show all the steps required, including intermediates, for the synthesis of the following target compound, using any starting material with six (6) carbons or less, plus any other organic or inorganic reagents necessary. Determine the IUPAC systematic chemical name for your target compound. Try for io sieps or tesvs
Synthesis Problem Show all the steps required, including intermediates, for the synthesis of the following target compound, using any starting material with six...
17. Outline the reactions necessary to accomplish the synthesis of the following compound starting from benzene....
17. Outline the reactions necessary to accomplish the synthesis of the following compound starting from benzene. Provide the necessary reagents/reactants and include the structure of intermediate organic products. Any additional organic starting materials used (excluding solvents) must not contain more than 3 carbons. You do not need to provide the mechanism of each reaction. ОН 18. Outline the reactions necessary to accomplish the synthesis of the following compound. Provide the necessary reagents/reactants and include the structure of intermediate organic products....
Show, by writing a series of synthetic steps how you could prepare the following target compound...
Show, by writing a series of synthetic steps how you could prepare the following target compound for the designated two starting materials (a cyclic diene and acetylene) and any other necessary organic or inorganic reagents. You must also show all the intermediate structure(s) for your synthesis indicated by the "?" marks. More than one step will be needed. H CH,CH, CH CHH + H-C=C-H ? ?
12. Propose a synthesis for the following compound using benzene or toluene and any other reagents...
12. Propose a synthesis for the following compound using benzene or toluene and any other reagents necessary. Show all major intermediate compounds that would probably be isolated during the course of your synthesis. (6 points)
Devise a synthesis of the following compound using the given compounds
Devise a synthesis of the following compound using the given compounds (you may use each one more than once if needed). You may also use any needed inorganic or organic reagents but all of the carbons in the target molecule must come from the given starting materials.
3:45 INFO Done Attachment H, Pt (excess) MY HO 2. Outline a synthesis starting from the...
3:45 INFO Done Attachment H, Pt (excess) MY HO 2. Outline a synthesis starting from the compound below and any other organic/inorganic compounds. Fill in the missing reagents and compound. Los OH PBr3 COOH 3. Propose how you could make the following compounds starting with benzene and any other organic or inorganic compounds.
What are the following syntheses for each compound? 7. Propose a synthesis for each of the...
What are the following syntheses for each compound?
7. Propose a synthesis for each of the following compounds using the indicated starting material. You may use any organic compounds, inorganic compounds, organometallic compounds, or solvents of your choice. Do not show any reactive intermediates, mechanisms, or transition states, but be sure to show each isolable compound along your synthetic route. осон steps H₂C (ra (racemic) Hoc OH Hac CH3 сна N-OH steps
QUESTION 12 Prepare the compound shown below from cyclohexanone (use as many molecules as needed) and...
QUESTION 12 Prepare the compound shown below from cyclohexanone (use as many molecules as needed) and organic compounds of three carbons or less as the starting materials. Show the product of each synthetic step and indicate all necessary reagents and reaction conditions. Count carbons carefully! os
b. Page 4 (Question 4 continued) Propose reasonable syntheses for the following indicated compounds and using...
b. Page 4 (Question 4 continued) Propose reasonable syntheses for the following indicated compounds and using any other necessary orga Show all intermediates formed to receive full credit ÇO2H I NO₂ for the following compounds beginning with the ng any other necessary organic or inorganic reagents. CHE SO3H OCH2CH3 [3% +6% marks] c. Outline the synthesis of the following compound using either the aceu meester synthesis method. Draw the structure of the starting material and show all intermediates, reagents and...
Predict the multiplicity M (the number of peaks as a result of
splitting) for each labeled proton in the following
compound.
H H H
Synthesis with 10 steps or less
Synthesis Problem Show all the steps required, including intermediates, for the synthesis of the following target compound, using any starting material with six (6) carbons or less, plus any other organic or inorganic reagents necessary. Determine the IUPAC systematic chemical name for your target compound. Try for io sieps or tesvs
Synthesis Problem Show all the steps required, including intermediates, for the synthesis of the following target compound, using any starting material with six...
17. Outline the reactions necessary to accomplish the synthesis of the following compound starting from benzene. Provide the necessary reagents/reactants and include the structure of intermediate organic products. Any additional organic starting materials used (excluding solvents) must not contain more than 3 carbons. You do not need to provide the mechanism of each reaction. ОН 18. Outline the reactions necessary to accomplish the synthesis of the following compound. Provide the necessary reagents/reactants and include the structure of intermediate organic products....
Show, by writing a series of synthetic steps how you could prepare the following target compound for the designated two starting materials (a cyclic diene and acetylene) and any other necessary organic or inorganic reagents. You must also show all the intermediate structure(s) for your synthesis indicated by the "?" marks. More than one step will be needed. H CH,CH, CH CHH + H-C=C-H ? ?
12. Propose a synthesis for the following compound using benzene or toluene and any other reagents necessary. Show all major intermediate compounds that would probably be isolated during the course of your synthesis. (6 points)
3:45 INFO Done Attachment H, Pt (excess) MY HO 2. Outline a synthesis starting from the compound below and any other organic/inorganic compounds. Fill in the missing reagents and compound. Los OH PBr3 COOH 3. Propose how you could make the following compounds starting with benzene and any other organic or inorganic compounds.
What are the following syntheses for each compound?
7. Propose a synthesis for each of the following compounds using the indicated starting material. You may use any organic compounds, inorganic compounds, organometallic compounds, or solvents of your choice. Do not show any reactive intermediates, mechanisms, or transition states, but be sure to show each isolable compound along your synthetic route. осон steps H₂C (ra (racemic) Hoc OH Hac CH3 сна N-OH steps
QUESTION 12 Prepare the compound shown below from cyclohexanone (use as many molecules as needed) and organic compounds of three carbons or less as the starting materials. Show the product of each synthetic step and indicate all necessary reagents and reaction conditions. Count carbons carefully! os
b. Page 4 (Question 4 continued) Propose reasonable syntheses for the following indicated compounds and using any other necessary orga Show all intermediates formed to receive full credit ÇO2H I NO₂ for the following compounds beginning with the ng any other necessary organic or inorganic reagents. CHE SO3H OCH2CH3 [3% +6% marks] c. Outline the synthesis of the following compound using either the aceu meester synthesis method. Draw the structure of the starting material and show all intermediates, reagents and...
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