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now how you would make the target compounds on the right form...
22. Show how you would make the target compounds on the right form the starting compounds on the left. Show reagent...
22. Show how you would make the target compounds on the right form the starting compounds on the left. Show reagents and conditions where appropriate, and the structures of important intermediate compounds. Do not show any (arrow pushing) mechanisms!!!! (8 points) NH2 3-Steps NH2 17. Show the products and give reaction mechanisms for the following, using curved arrows to indicate the flow of electrons between intermediates.
Question 5 (27 pts.) Synthesize the target) molecules on the right from the starting molecules the...
Question 5 (27 pts.) Synthesize the target) molecules on the right from the starting molecules the left. this can not be done in one reaction. Give reagents and conditions and the intermediate molecules at each step. Do not show any mechanisms or transient intermediates. If other isomers are formed at any step then you need to indicate this but you do not need to draw their structures. NOZ CO2H SO3H
Question 5 (27 pts.) Synthesize the target) molecules on the right from the starting molecules the...
Question 5 (27 pts.) Synthesize the target) molecules on the right from the starting molecules the left, this can not be done in one reaction. Give reagents and conditions and the intermediate molecules at each step. Do not show any mechanisms or transient intermediates. If other isomers are formed at any step then you need to indicate this but you do not need to draw their structures. NOZ CO2H SOH
52. Arrange the relative pKa's of the following compounds:( P (2 pts) соон соон COOH pKa's: 53. Arrange th compounds: (2 pts) e relative reaction rates for the electrophilic aromatic subst...
52. Arrange the relative pKa's of the following compounds:( P (2 pts) соон соон COOH pKa's: 53. Arrange th compounds: (2 pts) e relative reaction rates for the electrophilic aromatic substitution of the following CH3 OCHa NO2 Reaction rates: 54. Arrange the relative base strength of the following compounds: (2 pts) NHCOCH3 NH2 NH2 NH2 NH. OCH3 OCH3 Basicity 55. What is the splitting pattern for the labeled hydrogens in the following compounds? (5 pt CH CH 56. Provide one...
please answer completely and clearly. thank you! SHORT ANSWER #29: How would you carry out the...
please answer completely and clearly. thank you!
SHORT ANSWER #29: How would you carry out the synthesis below? Show the reagents needed for each step of your transformation, but do NOT draw the mechanisms for each step. (10 points) NH2 N SHORT ANSWER #29: How would you carry out the synthesis below? Show the reagents needed for each step of your transformation, but do NOT draw the mechanisms for each step. (10 points) NH2 N
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
Please answer and show all work. It is a multistep question. [1]. How do you prepare...
Please answer and show all work. It is a multistep
question.
[1]. How do you prepare the following compounds, starting from benzene? These synthesis require multiple steps, show all reagents and intermediate products CO2CH3 b.COM CH,CH3
This is really important. If you are 100% sure it is corect then thank you. 3....
This is really important. If you are 100% sure it is corect
then thank you.
3. Draw the appropriate starting materials and indicate the appropriate reaction conditions needed that you would need in order to make the ester shown below. There is more than one correct answer. (5 pts) La 4. Show reagents for the reactions below: (2 pts each, 6 pts total) OH CO-H os
(2) Show how you would prepare the following Compound from benzere include all reagents and intermediate...
(2) Show how you would prepare the following Compound from benzere include all reagents and intermediate structures Show all steps in mechanism for this reaction HCI CH3
Can you please answer all of them? Section B: Free Response (you must show your work...
Can you please answer all of them?
Section B: Free Response (you must show your work for full credit) 1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sp2 hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts) 2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect...
22. Show how you would make the target compounds on the right form the starting compounds on the left. Show reagents and conditions where appropriate, and the structures of important intermediate compounds. Do not show any (arrow pushing) mechanisms!!!! (8 points) NH2 3-Steps NH2 17. Show the products and give reaction mechanisms for the following, using curved arrows to indicate the flow of electrons between intermediates.
Question 5 (27 pts.) Synthesize the target) molecules on the right from the starting molecules the left. this can not be done in one reaction. Give reagents and conditions and the intermediate molecules at each step. Do not show any mechanisms or transient intermediates. If other isomers are formed at any step then you need to indicate this but you do not need to draw their structures. NOZ CO2H SO3H
Question 5 (27 pts.) Synthesize the target) molecules on the right from the starting molecules the left, this can not be done in one reaction. Give reagents and conditions and the intermediate molecules at each step. Do not show any mechanisms or transient intermediates. If other isomers are formed at any step then you need to indicate this but you do not need to draw their structures. NOZ CO2H SOH
52. Arrange the relative pKa's of the following compounds:( P (2 pts) соон соон COOH pKa's: 53. Arrange th compounds: (2 pts) e relative reaction rates for the electrophilic aromatic substitution of the following CH3 OCHa NO2 Reaction rates: 54. Arrange the relative base strength of the following compounds: (2 pts) NHCOCH3 NH2 NH2 NH2 NH. OCH3 OCH3 Basicity 55. What is the splitting pattern for the labeled hydrogens in the following compounds? (5 pt CH CH 56. Provide one...
please answer completely and clearly. thank you!
SHORT ANSWER #29: How would you carry out the synthesis below? Show the reagents needed for each step of your transformation, but do NOT draw the mechanisms for each step. (10 points) NH2 N SHORT ANSWER #29: How would you carry out the synthesis below? Show the reagents needed for each step of your transformation, but do NOT draw the mechanisms for each step. (10 points) NH2 N
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
Please answer and show all work. It is a multistep
question.
[1]. How do you prepare the following compounds, starting from benzene? These synthesis require multiple steps, show all reagents and intermediate products CO2CH3 b.COM CH,CH3
This is really important. If you are 100% sure it is corect
then thank you.
3. Draw the appropriate starting materials and indicate the appropriate reaction conditions needed that you would need in order to make the ester shown below. There is more than one correct answer. (5 pts) La 4. Show reagents for the reactions below: (2 pts each, 6 pts total) OH CO-H os
(2) Show how you would prepare the following Compound from benzere include all reagents and intermediate structures Show all steps in mechanism for this reaction HCI CH3
Can you please answer all of them?
Section B: Free Response (you must show your work for full credit) 1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sp2 hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts) 2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect...
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