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6. (12 pts) For each the molecules below, provide a retrosynthetic analysis and then give a...
4. (12 pts) For each of the molecules below, provide a retrosynthetic analysis to starting materials...
4. (12 pts) For each of the molecules below, provide a retrosynthetic analysis to starting materials that satisfy the conditions given. Then give a step-by-step synthetic plan. You may use any reagents you want to accomplish your synthesis. HC НОХ H₃C CH весна from propanal as the only carbon source from starting materials containing three or fewer carbon atoms
5. (12 pts) For the molecules below, provide a retrosynthetic analysis to starting materials that satisfy...
5. (12 pts) For the molecules below, provide a retrosynthetic analysis to starting materials that satisfy the conditions given. Then give a step-by-step synthetic plan. You may use any reagents you want to accomplish your synthesis. OH O from starting materials containing three or fewer carbon atoms from starting materials containing two or fewer carbon atoms
Retrosynthetic Analysis 12. Give a reasonable synthesis for each of the following compounds from the indicated...
Retrosynthetic Analysis 12. 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. NO MECHANISMS! [8 points] NH ONH2 Make starting with
4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place t...
4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. Me NH но HK он 1 4 5. 6. 3. 2. NH2 O) 08
4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. Me NH но HK он 1 4 5....
For any two of the molecules below, outline both a retrosynthetic analysis and a forward synthesis...
For any two of the molecules below, outline both a retrosynthetic analysis and a forward synthesis with reagents. Each of your building blocks should not incorporate more than five carbon atoms of the target molecule. (Note: your syntheses do not need to be stereoselective) COH OH [20 marks]
1- Suggest a retrosynthetic analysis for each of the following target molecules In each case identify...
1- Suggest a retrosynthetic analysis for each of the following
target molecules
In each case identify the latent polarity and the type of
disconnection .
2-suggest synthons, synthetic equivalents, and
reagents for the forward synthesis (a single disconnection is
required )
((resynthetic steps) , ((synthetic steps))
Please answer both When performing a retrosynthetic analysis for the desired synthesis below, what is the...
Please answer both
When performing a retrosynthetic analysis for the desired synthesis below, what is the best question to ask first? Br CH3-C=CH Br To what functional group can two adjacent bromine atoms be added? Which alkyl halide is needed for the synthesis? How can I deprotonate an alkyne? What reagents are needed to alkylate an alkyne? What is most likely the initial retrosynthetic disconnection of the target molecule in the given synthetic transformation (i.e., the last step of the...
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
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...
Please help by showing how to do the synthesis for both target molecules! Thank you and...
Please help by showing how to
do the synthesis for both target molecules! Thank you and please be
very thorough with explaining the solvents used and please also
provide a retrosynthetic anaylsis with the forward anaylsis.
Thanks!
7. (16 pts) Synthesize the target molecules using only the carbon sources provided and any reagents of your choosing. Target Molecules Carbon Sources Br Br HO CH3 CH
4. (12 pts) For each of the molecules below, provide a retrosynthetic analysis to starting materials that satisfy the conditions given. Then give a step-by-step synthetic plan. You may use any reagents you want to accomplish your synthesis. HC НОХ H₃C CH весна from propanal as the only carbon source from starting materials containing three or fewer carbon atoms
5. (12 pts) For the molecules below, provide a retrosynthetic analysis to starting materials that satisfy the conditions given. Then give a step-by-step synthetic plan. You may use any reagents you want to accomplish your synthesis. OH O from starting materials containing three or fewer carbon atoms from starting materials containing two or fewer carbon atoms
Retrosynthetic Analysis 12. 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. NO MECHANISMS! [8 points] NH ONH2 Make starting with
4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. Me NH но HK он 1 4 5. 6. 3. 2. NH2 O) 08
4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. Me NH но HK он 1 4 5....
For any two of the molecules below, outline both a retrosynthetic analysis and a forward synthesis with reagents. Each of your building blocks should not incorporate more than five carbon atoms of the target molecule. (Note: your syntheses do not need to be stereoselective) COH OH [20 marks]
1- Suggest a retrosynthetic analysis for each of the following
target molecules
In each case identify the latent polarity and the type of
disconnection .
2-suggest synthons, synthetic equivalents, and
reagents for the forward synthesis (a single disconnection is
required )
((resynthetic steps) , ((synthetic steps))
Please answer both
When performing a retrosynthetic analysis for the desired synthesis below, what is the best question to ask first? Br CH3-C=CH Br To what functional group can two adjacent bromine atoms be added? Which alkyl halide is needed for the synthesis? How can I deprotonate an alkyne? What reagents are needed to alkylate an alkyne? What is most likely the initial retrosynthetic disconnection of the target molecule in the given synthetic transformation (i.e., the last step of the...
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
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...
Please help by showing how to
do the synthesis for both target molecules! Thank you and please be
very thorough with explaining the solvents used and please also
provide a retrosynthetic anaylsis with the forward anaylsis.
Thanks!
7. (16 pts) Synthesize the target molecules using only the carbon sources provided and any reagents of your choosing. Target Molecules Carbon Sources Br Br HO CH3 CH
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