I ONLY NEED HELP WITH THE SECOND COLUMN (NOT THE FIRST)
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I ONLY NEED HELP WITH THE SECOND COLUMN (NOT THE
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Second Column only for synthesis!!...
need help on synthesis 9 10-Synthesis question. Show how the starting material can be converted to...
need help on synthesis
9 10-Synthesis question. Show how the starting material can be converted to the product through any of the reactions you have learned in Ochem-l and Ochem-II. Show all the reagents you need and indicate the stereochemistry when appropriate. You do not need to show arrow pushing like in a mechanism question, only the reactions. If a chiral molecule is formed mark the chiral center with an asterisk (*) and write "racemic" below the structure. All carbon...
i need help with these synthesis problems: a,b,c 3) Show how the following molecules can be synthesized from the sta...
i need help with these synthesis problems: a,b,c
3) Show how the following molecules can be synthesized from the starting material indicated. Draw the structure of each intermediary compound in your synthesis, and add reagents above/beneath your reaction arrows. (24 points total). CHO HOH CHO HOH H -OH H-OH HOH H- OH НТОН CH OM CH OH DOH Cros Co ^Nitz DEN ĮHz, Pd-c 17 -NO₂ Page 3 of 5
ChemActivity 10: Oxidation and Reduction 149 7. Show a synthesis of each of the following target...
ChemActivity 10: Oxidation and Reduction 149 7. Show a synthesis of each of the following target molecules from methylenecyclohexane. (Some syntheses may be only one step.) methylenecyclohexane (starting material) OH -CC-CH₂ OH OH OH _LOH OCH OH- 8 Draw the product that results when each set of reagents is mixed with methyeyclohexene 1) BHS THE HBr peroxides 2) HOOH NAOH HCI 1) Hg(OAc), THF, H2O 2) NaBH, NaOH Bry Pd 0°, dark, no peroxides Pd 1) MCPBA 2) H SO./...
Synthesis using Carbonyla-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry....
Synthesis using Carbonyla-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry. You are assigned two target molecules, one of which is best synthesized by an alkylation approach, while the other is best synthesized by an addition or condensation approach. My two target molecules are number 2 and number 12 in the last page. You must do the following: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the...
Page 1 Synthesis using Carbonyl O-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules...
Page 1 Synthesis using Carbonyl O-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry. You are assigned two target molecules, one of which is best synthesized by an alkylation approach, while the other is best synthesized by an addition or condensation approach. You must do the following: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the organic starting material (what you have to work backwards toward) depends...
Can someone help me solve this synthesis? Q 10 - Synthesis question. Show how the starting...
Can someone help me solve this synthesis?
Q 10 - Synthesis question. Show how the starting material can be converted to the product through any of the reactions you have learned in Ochem-I and Ochem-11. Show all the reagents you need and indicate the stereochemistry when appropriate. You do not need to show arrow pushing like in a mechanism question, only the reactions. If a chiral molecule is formed mark the chiral center with an asterisk (") and write "racemic"...
Synthesis question... I just need help with the structures. Thanks Devise a synthesis of CH3CH2CECCH2CH2OH using...
Synthesis question... I just need help with the structures.
Thanks
Devise a synthesis of CH3CH2CECCH2CH2OH using CH3CH2CH- CH2 as the starting material. You may use any other organic compounds or inorganic reagents. Be sure to answer all parts. OH Step 1 LICI 2 equiv CI2 SOCI Intermediate 1: edit structure
Use retrosynthesis to design a synthesis of each target using the starting material and any reagents...
Use retrosynthesis to design a synthesis of each target using the starting material and any reagents containing three carbons or less. 5. Target Starting Material Target Starting Material OH COH H C Dis Explain why an electron pair in an sp hybrid orbital is lower in potential energy than an electron pair in an sp hybrid 6. H orbital. Explain why ethy ne is more acidic than 7 ethene or ethane. H-CRCE pk, s0 Construct an explanation for why the...
Need Help. Will Rate If Complete. Q 8- The following molecules can be formed by either:...
Need Help. Will Rate If Complete.
Q 8- The following molecules can be formed by either: Michael Reaction; Enamine Acylation; Acetoacetic Ester Synthesis; Michael Addition; Malonic Ester Synthesis; Robinson Annulation; Aldol Condensation; Claisen Condensation; Intramolecular Aldol Condensation; Dieckmann Condensation or a Combination of two of the above listed reaction. In each case write the proper of the reaction on the line and dissect the product into appropriate starting material. In some cases there might only be one starting material. You...
I just need help with the assessment section Lab Section Name Write-Up Sheet for Multi-step Synthesis...
I just need help with the assessment section
Lab Section Name Write-Up Sheet for Multi-step Synthesis Experiment (Day 2) Give the reaction scheme (starting material(s), reagents, ex heme (starting material(s), reagents, expected product) for the second step of your multi- step synthesis. Solvents and catalysts should be included though work up steps need not be shown. O Tethanolo 2-(Phenylamino) phano DATA & ANALYSIS N - Playl-2-hylony beneylumine Amounts of Starting Materials and Reagents Used List all starting materials and reagents...
need help on synthesis
9 10-Synthesis question. Show how the starting material can be converted to the product through any of the reactions you have learned in Ochem-l and Ochem-II. Show all the reagents you need and indicate the stereochemistry when appropriate. You do not need to show arrow pushing like in a mechanism question, only the reactions. If a chiral molecule is formed mark the chiral center with an asterisk (*) and write "racemic" below the structure. All carbon...
i need help with these synthesis problems: a,b,c
3) Show how the following molecules can be synthesized from the starting material indicated. Draw the structure of each intermediary compound in your synthesis, and add reagents above/beneath your reaction arrows. (24 points total). CHO HOH CHO HOH H -OH H-OH HOH H- OH НТОН CH OM CH OH DOH Cros Co ^Nitz DEN ĮHz, Pd-c 17 -NO₂ Page 3 of 5
ChemActivity 10: Oxidation and Reduction 149 7. Show a synthesis of each of the following target molecules from methylenecyclohexane. (Some syntheses may be only one step.) methylenecyclohexane (starting material) OH -CC-CH₂ OH OH OH _LOH OCH OH- 8 Draw the product that results when each set of reagents is mixed with methyeyclohexene 1) BHS THE HBr peroxides 2) HOOH NAOH HCI 1) Hg(OAc), THF, H2O 2) NaBH, NaOH Bry Pd 0°, dark, no peroxides Pd 1) MCPBA 2) H SO./...
Synthesis using Carbonyla-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry. You are assigned two target molecules, one of which is best synthesized by an alkylation approach, while the other is best synthesized by an addition or condensation approach. My two target molecules are number 2 and number 12 in the last page. You must do the following: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the...
Page 1 Synthesis using Carbonyl O-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry. You are assigned two target molecules, one of which is best synthesized by an alkylation approach, while the other is best synthesized by an addition or condensation approach. You must do the following: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the organic starting material (what you have to work backwards toward) depends...
Can someone help me solve this synthesis?
Q 10 - Synthesis question. Show how the starting material can be converted to the product through any of the reactions you have learned in Ochem-I and Ochem-11. Show all the reagents you need and indicate the stereochemistry when appropriate. You do not need to show arrow pushing like in a mechanism question, only the reactions. If a chiral molecule is formed mark the chiral center with an asterisk (") and write "racemic"...
Synthesis question... I just need help with the structures.
Thanks
Devise a synthesis of CH3CH2CECCH2CH2OH using CH3CH2CH- CH2 as the starting material. You may use any other organic compounds or inorganic reagents. Be sure to answer all parts. OH Step 1 LICI 2 equiv CI2 SOCI Intermediate 1: edit structure
Use retrosynthesis to design a synthesis of each target using the starting material and any reagents containing three carbons or less. 5. Target Starting Material Target Starting Material OH COH H C Dis Explain why an electron pair in an sp hybrid orbital is lower in potential energy than an electron pair in an sp hybrid 6. H orbital. Explain why ethy ne is more acidic than 7 ethene or ethane. H-CRCE pk, s0 Construct an explanation for why the...
Need Help. Will Rate If Complete.
Q 8- The following molecules can be formed by either: Michael Reaction; Enamine Acylation; Acetoacetic Ester Synthesis; Michael Addition; Malonic Ester Synthesis; Robinson Annulation; Aldol Condensation; Claisen Condensation; Intramolecular Aldol Condensation; Dieckmann Condensation or a Combination of two of the above listed reaction. In each case write the proper of the reaction on the line and dissect the product into appropriate starting material. In some cases there might only be one starting material. You...
I just need help with the assessment section
Lab Section Name Write-Up Sheet for Multi-step Synthesis Experiment (Day 2) Give the reaction scheme (starting material(s), reagents, ex heme (starting material(s), reagents, expected product) for the second step of your multi- step synthesis. Solvents and catalysts should be included though work up steps need not be shown. O Tethanolo 2-(Phenylamino) phano DATA & ANALYSIS N - Playl-2-hylony beneylumine Amounts of Starting Materials and Reagents Used List all starting materials and reagents...
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