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Retrosynthetic Analysis 12. Give a reasonable synthesis for each of the following compounds from the indicated...
Give a reasonable synthesis for each of the following compounds from the indicated starting materials. You...
Give a reasonable synthesis for
each of the following compounds from the indicated starting
materials. You may use any other organic or inorganic reagents you
wish unless otherwise indicated. The desired product for each
reaction you propose must be the one of the predominant products.
Give the reactants, conditions (where appropriate) and products of
each synthetic step. If equal mixtures are anticipated (i.e. ortho
/ para products) then indicate where separations are needed. NO
MECHANISMS! [6 points
2. Give a...
please explain why the answer is the answer step by step Retrosynthetic Analysis Give a reasonable...
please explain why the answer is the answer step by step
Retrosynthetic Analysis Give a reasonable synthesis for each of the following compounds from the indicated starting materials. You may use any other organic or inorganic reagents you wish unless otherwise indicated. The desired product for each reaction you propose must be the one of the predominant products. Give the reactants, conditions (where appropriate) and products of each synthetic step. If equal mixtures are anticipated (ie. ortho/para products) then indicate...
Synthesis 10. Give a reasonable synthesis for the following compound from the indicated starting material. You...
Synthesis 10. Give a reasonable synthesis for the following compound from the indicated starting material. You may use any other organic or inorganic reagents you wish unless otherwise indicated. The desired product for each reaction you propose must be the one of the predominant products. Give the reactants, conditions (where appropriate) and products of each synthetic step. NO MECHANISMS! [6 points) Make med og som en ons starting with SO3H
9.RETROSYNTHETIC ANALYSIS Give a reasonable synthesis for the following compound from the indicated starting materials. You...
9.RETROSYNTHETIC ANALYSIS Give a reasonable synthesis for the following compound from the indicated starting materials. You may use any other organic reagents or inorganic reagents you wish. The desired product for each reaction must be the MAJOR PRODUCT. Give the reactants, conditions (where appropriate), and products of each synthetic step but NO MECHANISMS. [4 points) OH Use to make HO
7. MECHANISM: Give the complete stepwise mechanism to account for the following observation. Use curved arrows...
7. MECHANISM: Give the complete stepwise mechanism to account for the following observation. Use curved arrows to show FLOW OF ELECTRONS. [9 points H-CI 8.RETROSYNTHETIC ANALYSIS Give a reasonable synthesis for the following compound from the indicated starting materials. You may use any other organic reagents or inorganic reagents you wish. The desired product for each reaction must be the MAJOR PRODUCT. Give the reactants, conditions (where appropriate), and products of each synthetic step but NO MECHANISMS. [6 points] OH...
Perform a retrosynthetic analysis of the compounds below and then devise their synthesis from readily available...
Perform a retrosynthetic analysis of the compounds below and
then devise their synthesis from readily available starting
compounds and any inorganic and/ or organic reagents. Your answer
should include a complete retrosynthetic analysis, synthesis
pathway with reagents and reaction conditions.
Ph Ph from Ph Ph from
Need D,E & G. outline a reaction sequence for synthesis of each of the following compounds fr...
need D,E & G. outline a reaction sequence for synthesis of each
of the following compounds from the indicated starting material
& any other organic or inorganic reagents needed.
Outline a reaction sequence for synthesis of each of the following compounds from the indicated starting material and any other organic or inorganic reagents needed. (a) 0 0 0 он OEt он ,EUA 853 PROBLEMS NH+ (g) O OEt OE
Outline a reaction sequence for synthesis of each of the following...
FALL 2019 QUIZNIO 1 Draw the MAJOR organic products of each reaction and indicate stereochemistry where...
FALL 2019 QUIZNIO 1 Draw the MAJOR organic products of each reaction and indicate stereochemistry where necessary (4 points SOCIE нанд tok OMSO HCI (2 e) 2 SYNTHESIS: How would you prepare compound 1 from cyclopentanol? You may use any other organic reagents of inorganic reagents you wish but you must start with cyclopentanol. The desired product for each reaction must be the MAJOR PRODUCT. Give the reactants, conditions (where appropriate and products of each synthetic step but NO MECHANISMS....
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...
6. (12 pts) For each the molecules below, provide a retrosynthetic analysis and then give a...
6. (12 pts) For each the molecules below, provide a retrosynthetic analysis and then give a step-by- step synthetic plan. All the carbon atoms in the final products must come from molecules in the box at the bottom. You may use any other reagents you want to accomplish your synthesis. H3CH2CO Acceptable Carbon Sources: " i hool.com ormar BCH,NH iicuch " OCH CH3
Give a reasonable synthesis for
each of the following compounds from the indicated starting
materials. You may use any other organic or inorganic reagents you
wish unless otherwise indicated. The desired product for each
reaction you propose must be the one of the predominant products.
Give the reactants, conditions (where appropriate) and products of
each synthetic step. If equal mixtures are anticipated (i.e. ortho
/ para products) then indicate where separations are needed. NO
MECHANISMS! [6 points
2. Give a...
please explain why the answer is the answer step by step
Retrosynthetic Analysis Give a reasonable synthesis for each of the following compounds from the indicated starting materials. You may use any other organic or inorganic reagents you wish unless otherwise indicated. The desired product for each reaction you propose must be the one of the predominant products. Give the reactants, conditions (where appropriate) and products of each synthetic step. If equal mixtures are anticipated (ie. ortho/para products) then indicate...
Synthesis 10. Give a reasonable synthesis for the following compound from the indicated starting material. You may use any other organic or inorganic reagents you wish unless otherwise indicated. The desired product for each reaction you propose must be the one of the predominant products. Give the reactants, conditions (where appropriate) and products of each synthetic step. NO MECHANISMS! [6 points) Make med og som en ons starting with SO3H
9.RETROSYNTHETIC ANALYSIS Give a reasonable synthesis for the following compound from the indicated starting materials. You may use any other organic reagents or inorganic reagents you wish. The desired product for each reaction must be the MAJOR PRODUCT. Give the reactants, conditions (where appropriate), and products of each synthetic step but NO MECHANISMS. [4 points) OH Use to make HO
7. MECHANISM: Give the complete stepwise mechanism to account for the following observation. Use curved arrows to show FLOW OF ELECTRONS. [9 points H-CI 8.RETROSYNTHETIC ANALYSIS Give a reasonable synthesis for the following compound from the indicated starting materials. You may use any other organic reagents or inorganic reagents you wish. The desired product for each reaction must be the MAJOR PRODUCT. Give the reactants, conditions (where appropriate), and products of each synthetic step but NO MECHANISMS. [6 points] OH...
Perform a retrosynthetic analysis of the compounds below and
then devise their synthesis from readily available starting
compounds and any inorganic and/ or organic reagents. Your answer
should include a complete retrosynthetic analysis, synthesis
pathway with reagents and reaction conditions.
Ph Ph from Ph Ph from
need D,E & G. outline a reaction sequence for synthesis of each
of the following compounds from the indicated starting material
& any other organic or inorganic reagents needed.
Outline a reaction sequence for synthesis of each of the following compounds from the indicated starting material and any other organic or inorganic reagents needed. (a) 0 0 0 он OEt он ,EUA 853 PROBLEMS NH+ (g) O OEt OE
Outline a reaction sequence for synthesis of each of the following...
FALL 2019 QUIZNIO 1 Draw the MAJOR organic products of each reaction and indicate stereochemistry where necessary (4 points SOCIE нанд tok OMSO HCI (2 e) 2 SYNTHESIS: How would you prepare compound 1 from cyclopentanol? You may use any other organic reagents of inorganic reagents you wish but you must start with cyclopentanol. The desired product for each reaction must be the MAJOR PRODUCT. Give the reactants, conditions (where appropriate and products of each synthetic step but NO MECHANISMS....
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...
6. (12 pts) For each the molecules below, provide a retrosynthetic analysis and then give a step-by- step synthetic plan. All the carbon atoms in the final products must come from molecules in the box at the bottom. You may use any other reagents you want to accomplish your synthesis. H3CH2CO Acceptable Carbon Sources: " i hool.com ormar BCH,NH iicuch " OCH CH3
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