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4. Synthesize the following compound from starting materials containing the indi cated number of carbons. Show your syntheses in the forward direction and include any necessary reactants, reagents or...
3. (15 pts.) Provide retro- and forward syntheses of the following compound from the indicated starting...
3. (15 pts.) Provide retro- and forward syntheses of the following compound from the indicated starting materials. Show all reagents required for each transformation. Individual amino acids NCO2H NH2 H21
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....
11. Propose a synthesis for each compound below. You must write in all necessary reactants, reagents,...
11. Propose a synthesis for each compound below. You must write in all necessary reactants, reagents, and solvents to receive full credit. Your starting materials must be 3 carbons or less. If you use an ionic or organometallic species, you must show how it was synthesized from a neutral, covalent species. Any species that adds carbon to your product must be synthesized from a molecule of 3 carbons or less. Only show the steps of your synthesis- do not put...
4) (2 pts each) Outline a synthesis (i.e., simply show the reagents/reactants for the necessary reactions)...
4) (2 pts each) Outline a synthesis (i.e., simply show the reagents/reactants for the necessary reactions) for each compound below from the designated starting material. Use reagents you've learned about in Orgo I and II. The number of arrows does not necessarily correspond to the number of steps required. As a general rule, any carbon units in the products that were not in the starting materials should come from molecules containing 7 or fewer carbons. Things that don't end up...
4. Show how to synthesize the following products using any reactants/reagents and number of steps (unless...
4. Show how to synthesize the following products using any reactants/reagents and number of steps (unless otherwise specified below). Be sure to show all reactants/reagents/conditions required HO from
2. Design multi-step syntheses for TWO of the following targets. Show the reagents needed for each...
2. Design multi-step syntheses for TWO of the following targets. Show the reagents needed for each step and the product of each step. Special conditions: You must use cyclopentadiene as your starting material for all syntheses. You may use organic reagents containing 4 or fewer carbons, and any inorganic reagents. For any Diels-Alder reaction that you use (necessary for all targets!), the dienophile must be an a,ß-unsaturated carbonyl compound. Target 1: HO D Target 2: Doe Target 3: ro Target...
1. Provide a complete retrosynthesis and forward synthesis of the target molecule below from the given...
1. Provide a complete retrosynthesis and forward synthesis of the target molecule below from the given starting materials. All carbons of the target must be from the given starting materials. You may use any reagents you find necessary. You may include more than one step over a reaction arrow, but please no more than 3 steps at a time. Please show the key intermediates in your synthesis for partial credit. (10 bonus points) For full credit, include a retrosynthetic analysis,...
Need help, numbers 3-6 please show work. and fill out table of chemicals for all chemical...
Need help, numbers 3-6 please show work. and fill out table of
chemicals for all chemical used.
calculate mmol in the table as well show work please
and each of these must be listed in its own row. There are 10 column headings: IUPAC name OR common name, structure, CAS number (Chemical Abstract Service number) molecular mass, melting point (if applicable), boiling point (if applicable), solubility (in water, if applicable), density, amounts to be used in the experiment, and the...
3. (15 pts.) Provide retro- and forward syntheses of the following compound from the indicated starting materials. Show all reagents required for each transformation. Individual amino acids NCO2H NH2 H21
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....
11. Propose a synthesis for each compound below. You must write in all necessary reactants, reagents, and solvents to receive full credit. Your starting materials must be 3 carbons or less. If you use an ionic or organometallic species, you must show how it was synthesized from a neutral, covalent species. Any species that adds carbon to your product must be synthesized from a molecule of 3 carbons or less. Only show the steps of your synthesis- do not put...
4) (2 pts each) Outline a synthesis (i.e., simply show the reagents/reactants for the necessary reactions) for each compound below from the designated starting material. Use reagents you've learned about in Orgo I and II. The number of arrows does not necessarily correspond to the number of steps required. As a general rule, any carbon units in the products that were not in the starting materials should come from molecules containing 7 or fewer carbons. Things that don't end up...
4. Show how to synthesize the following products using any reactants/reagents and number of steps (unless otherwise specified below). Be sure to show all reactants/reagents/conditions required HO from
2. Design multi-step syntheses for TWO of the following targets. Show the reagents needed for each step and the product of each step. Special conditions: You must use cyclopentadiene as your starting material for all syntheses. You may use organic reagents containing 4 or fewer carbons, and any inorganic reagents. For any Diels-Alder reaction that you use (necessary for all targets!), the dienophile must be an a,ß-unsaturated carbonyl compound. Target 1: HO D Target 2: Doe Target 3: ro Target...
1. Provide a complete retrosynthesis and forward synthesis of the target molecule below from the given starting materials. All carbons of the target must be from the given starting materials. You may use any reagents you find necessary. You may include more than one step over a reaction arrow, but please no more than 3 steps at a time. Please show the key intermediates in your synthesis for partial credit. (10 bonus points) For full credit, include a retrosynthetic analysis,...
Need help, numbers 3-6 please show work. and fill out table of
chemicals for all chemical used.
calculate mmol in the table as well show work please
and each of these must be listed in its own row. There are 10 column headings: IUPAC name OR common name, structure, CAS number (Chemical Abstract Service number) molecular mass, melting point (if applicable), boiling point (if applicable), solubility (in water, if applicable), density, amounts to be used in the experiment, and the...
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