he wants the steps. what should you add to get this reaction from the cycloheanone.
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Birch Reduction(Li/liq.NH3, NH4Cl) reduces enone to Ketone.
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he wants the steps. what should you add to get this reaction from the cycloheanone. (10)...
1) Propose a synthesis of the following amine from ethanol. Ethanol should be the only carbon...
1) Propose a synthesis of the following amine from ethanol. Ethanol should be the only carbon source you use. 2) Propose a synthesis. 3) Propose a synthesis. 1) PCC pn. 3)acid work up 5) 03 6) DMS 7)? 8)? 9) H/Ni 4) Propose a synthesis. 5) Name the following using IUPAC nomenclature.
16. Provide the final product of the following reaction. Name the reaction. 17. Provide the major...
16. Provide the final product of the following reaction. Name the reaction. 17. Provide the major organic product of the following reaction. What is the name of the reaction? MCPBA 18. Using ethanol as your only source of carbon compounds and using any other necessary inorganic reagents, propose a synthesis of ethyl ethanoate. Show each reaction step. O Type here to search oe剆自
1) Propose a synthesis of the following amine from ethanol. Ethanol should be the only carbon...
1) Propose a synthesis of the following amine from ethanol. Ethanol should be the only carbon source you use. Lfcce HN 2) Propose a synthesis. OH 3) Propose a synthesis. Ph OH 1) PCC 2) 3)acid work up 4)2 NH 5) O3, 6) DMS 7)? 8)? 9) H2/Ni 4) Propose a synthesis. HN 5) Name the following using IUPAC nomenclature. Br
please answer and show work for stepwise synthesis and other questions. 1. Provide a stepwise synthesis...
please answer and show work for stepwise synthesis and other
questions.
1. Provide a stepwise synthesis for the dipeptide Ser-Phe. Draw all steps including protecting groups. H2N-CH-C-OH H2N-CH-C-OH CH2 Phe Ser 2. Using ethyl 3-methylbutanoate as your only source of carbon and using any other reagents necessary, propose a stepwise synthesis for the following conversion. 3. Provide the reagents necessary to carry out the following conversion. 4. Provide the structures of the products in each step of the following reaction...
Show your steps and reaction conditions clearly. No reaction mechanisms are required. (a) Using acetone and...
Show your steps and reaction conditions clearly. No reaction mechanisms are required. (a) Using acetone and 2.2-dimethylpropanal as your only sources of carbon atoms, show how you would synthesize compound 1. Hint: Reaction of a diol and a carbonyl compound. Starting from 1-ethoxynaphthalene and 3-methylbutanoic acid as your only sources of carbon atoms, show how you would synthesize the ester 1. Hint oxidation of a ketone to ester (C) Suggest a synthesis for compound 1 using as starting materials/reactants benzaldehye....
(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....
4. Propose a synthesis to create 3,4-dimethyl-3-hexanol from 1-butene. You only need to show individual steps an...
4. Propose a synthesis to create 3,4-dimethyl-3-hexanol from 1-butene. You only need to show individual steps and reagents, you do not need to show mechanisms. You must use 1-butene as your ONLY source of carbon atoms. The convergent processes have been outlined for you. for STEP 1: Show how to synthesize butyl magnesium bromide from 1-butene (5 points): BrMg STEP 2: Show how to synthesize 2-butanone from 1-butene (5 points): STEP 3: What intermediate forms below and what reagent(s) will...
(12 pts total) 21-23. Mechanisms: Provide a reasonable, detailed, stepwise mechanism for: (4 pts, all, if...
(12 pts total) 21-23. Mechanisms: Provide a reasonable, detailed, stepwise mechanism for: (4 pts, all, if completely correct, or nothing) 21. ... the base-promoted transesterification of methyl benzoate with sodium ethoxide. (4 pts, all, if completely correct, or nothing) 22. ... the acid-catalyzed enolization of acetaldehyde. (4 pts, all, if completely correct, or nothing) 23. ... the base-promoted enolization of chloropropanone. (16 pts total) 24-25. Multistep Syntheses: propose a reasonable, efficient, effective, elegant, good-yield synthesis, providing the appropriate reagents and/or...
3 Propose a mechanism for the following reaction. Show all steps Show all nonzero formal charges...
3 Propose a mechanism for the following reaction. Show all steps Show all nonzero formal charges Show all important resonance forms of intermediates Use curved arrows to show electron flow н* NH Ph сн,осн, Hо Ph CH,осH, COCHS CHEGCHS CHyait Ph Ph Ph CHZOC WH3 4. Propose a synthesis of 2-butanol (CH;CHOHCH;CH3) starting with ethanol (CH,CH:OH) as your only source of carbons in the product. You may use any other reagents or solvents as long as they do not contribute...
(10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the...
(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. Show all reaction steps, reagents and conditions used. OH ethanol 4-methylheptan-4-01
1) Propose a synthesis of the following amine from ethanol. Ethanol should be the only carbon source you use. 2) Propose a synthesis. 3) Propose a synthesis. 1) PCC pn. 3)acid work up 5) 03 6) DMS 7)? 8)? 9) H/Ni 4) Propose a synthesis. 5) Name the following using IUPAC nomenclature.
16. Provide the final product of the following reaction. Name the reaction. 17. Provide the major organic product of the following reaction. What is the name of the reaction? MCPBA 18. Using ethanol as your only source of carbon compounds and using any other necessary inorganic reagents, propose a synthesis of ethyl ethanoate. Show each reaction step. O Type here to search oe剆自
1) Propose a synthesis of the following amine from ethanol. Ethanol should be the only carbon source you use. Lfcce HN 2) Propose a synthesis. OH 3) Propose a synthesis. Ph OH 1) PCC 2) 3)acid work up 4)2 NH 5) O3, 6) DMS 7)? 8)? 9) H2/Ni 4) Propose a synthesis. HN 5) Name the following using IUPAC nomenclature. Br
please answer and show work for stepwise synthesis and other
questions.
1. Provide a stepwise synthesis for the dipeptide Ser-Phe. Draw all steps including protecting groups. H2N-CH-C-OH H2N-CH-C-OH CH2 Phe Ser 2. Using ethyl 3-methylbutanoate as your only source of carbon and using any other reagents necessary, propose a stepwise synthesis for the following conversion. 3. Provide the reagents necessary to carry out the following conversion. 4. Provide the structures of the products in each step of the following reaction...
Show your steps and reaction conditions clearly. No reaction mechanisms are required. (a) Using acetone and 2.2-dimethylpropanal as your only sources of carbon atoms, show how you would synthesize compound 1. Hint: Reaction of a diol and a carbonyl compound. Starting from 1-ethoxynaphthalene and 3-methylbutanoic acid as your only sources of carbon atoms, show how you would synthesize the ester 1. Hint oxidation of a ketone to ester (C) Suggest a synthesis for compound 1 using as starting materials/reactants benzaldehye....
(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....
4. Propose a synthesis to create 3,4-dimethyl-3-hexanol from 1-butene. You only need to show individual steps and reagents, you do not need to show mechanisms. You must use 1-butene as your ONLY source of carbon atoms. The convergent processes have been outlined for you. for STEP 1: Show how to synthesize butyl magnesium bromide from 1-butene (5 points): BrMg STEP 2: Show how to synthesize 2-butanone from 1-butene (5 points): STEP 3: What intermediate forms below and what reagent(s) will...
(12 pts total) 21-23. Mechanisms: Provide a reasonable, detailed, stepwise mechanism for: (4 pts, all, if completely correct, or nothing) 21. ... the base-promoted transesterification of methyl benzoate with sodium ethoxide. (4 pts, all, if completely correct, or nothing) 22. ... the acid-catalyzed enolization of acetaldehyde. (4 pts, all, if completely correct, or nothing) 23. ... the base-promoted enolization of chloropropanone. (16 pts total) 24-25. Multistep Syntheses: propose a reasonable, efficient, effective, elegant, good-yield synthesis, providing the appropriate reagents and/or...
3 Propose a mechanism for the following reaction. Show all steps Show all nonzero formal charges Show all important resonance forms of intermediates Use curved arrows to show electron flow н* NH Ph сн,осн, Hо Ph CH,осH, COCHS CHEGCHS CHyait Ph Ph Ph CHZOC WH3 4. Propose a synthesis of 2-butanol (CH;CHOHCH;CH3) starting with ethanol (CH,CH:OH) as your only source of carbons in the product. You may use any other reagents or solvents as long as they do not contribute...
(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. Show all reaction steps, reagents and conditions used. OH ethanol 4-methylheptan-4-01
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