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Each of the following Williamson ether...
How would you prepare benzyl methyl ether using a Williamson ether synthesis? The list of reagents...
How would you prepare benzyl methyl ether using a Williamson ether synthesis? The list of reagents to choose from are: 2-Chloro-norborane, Benzyl chloride, 2-Chloro-2-methylpropane, 4-Chloro-1-butanol, and Chlorobutane. I was reading online and it kept mentioning SN2 reactions, using an alcohol, and an alkyl halide for the synthesis. My guess would be using Benzyl Chloride and another one with an OH attached, but I could be completely wrong. Please help and explain by showing the reaction mechanism. Thank you so much!...
4) Briefly explain why the following molecule cannot be produced using Williamson ether synthesis. 4 pts...
4) Briefly explain why the following molecule cannot be produced using Williamson ether synthesis. 4 pts Note: a complete answer will illustrate the two theoretical William ether synthetic pathways that could be used to synthesis the product (1 pt each) and explain why each pathway would not yield the desired product (1 pt each). Bonus: Provide a different synthetic pathway that produces the ether shown above. (I could do it in a single step!). (bonus 2 pts).
3. Show reagents that you could use to prepare the following ether via a Williamson ether...
3. Show reagents that you could use to prepare the following ether via a Williamson ether synthesis and explain your reasoning.
please answer these questions. thanks 1. Write a reaction of the Williamson Ether synthesis of your...
please answer these questions. thanks
1. Write a reaction of the Williamson Ether synthesis of your product. 2. In this acid catalyzed reaction, a stable benzylic carbocation is formed. Show how this carbocation is formed. 3. Write resonance forms for the benzylic carbocation that is formed. 4. Use the government website www.uspto.gov to find the patent number for the synthesis of your product. Step 2: Ether Synthesis он OR NaBH ROH Amberlyst-15 NaoH H,O он он он
please answer question number Questions: 1. Show, by equations, how you would prepare phenylbenzyl ether by...
please answer question number
Questions: 1. Show, by equations, how you would prepare phenylbenzyl ether by the familiar Williamson synthesis. 2. In the preparation of methyl-2-napthoxy ether: A. What substances are present after the final reflux period? B. What serves as the nucleophile? C. How is the product purified? 3. In your preparation of 2,4-dinitrophenyl-p-tolylamine: In A. How is excess amine removed from the product? B. What serves as the nucleophile?
Please explain the folllwing thoroughly. Pictures will help! Thank you very much. increase in o ncrease...
Please explain the folllwing thoroughly. Pictures will help! Thank
you very much.
increase in o ncrease in H2 CH2 -16, which would be the best way to carry out the following synthesis? OH Br a. (1) KOH, C2HsOH; (2) BH3:THF, then H202, OH b. (1) (CHb)aCOK/(CHs)jbCOH: (2) Ha0, then H20, heat c. (1) HA, heat; (2) H30*, H2O, heat d. (1) (CHa)sCOK/(CHs) COH; (2) BHs:THF, then H202, OH e. (1) KOH, C2HsOH: (2) HA, heat; (3) H30*, H2O, heat -17....
please explain how you got your answer, i am completely lost Use synthetic division to determine...
please explain how you got your answer, i am completely lost
Use synthetic division to determine whether iis a zero of the function. Show all work to receive credit. Give a reason for your answer. (2 points) f(x) = x4 - 2x3 + 4x2 - 2x + 3 Zero? e synthetic division and the remainder theorem to find the zeros of the function. Sh
Please explain how you got the answer for this, for some reason I can not grasp...
Please explain how you got the answer for this, for some reason I can not grasp how to choose from those answer choices... BUT I do know how to get the Qc... Thanks so much for your help and please explain as simply as possible For the reaction H2(g) + Br2(g) 2HBr(g), Kc = 81.4 at 385C. If [H2] = [Br2] = [HBr] = 2.4 10-4 M at 385C, which one of the following is correct? A. [H2] and [HBr]...
Please explain clearly how they got the answer, thank you! Please explain clearly how they got...
Please explain clearly how they
got the answer, thank you!
Please explain clearly how they got the answer, thank you! A proton is accelerated from rest through a potential difference of 2.5 kV and then moves perpendicularly through a uniform 0.60-T magnetic field. What is the radius of the resulting path?
Can you please explain how you got your answer? Thank you! For each of the following...
Can you please explain how you got your answer? Thank you!
For each of the following compounds, determine whether or not you would expect its IR spectrum to exhibit a signal to the left of 3000 cm1: Yes, we expect a signal above 3000 cm-1. O No, we do not expect a signal above 3000 cm-1. Yes, we expect a signal above 3000 cm-1. No, we do not expect a signal above 3000 cm-1. Yes, we expect a signal above...
4) Briefly explain why the following molecule cannot be produced using Williamson ether synthesis. 4 pts Note: a complete answer will illustrate the two theoretical William ether synthetic pathways that could be used to synthesis the product (1 pt each) and explain why each pathway would not yield the desired product (1 pt each). Bonus: Provide a different synthetic pathway that produces the ether shown above. (I could do it in a single step!). (bonus 2 pts).
3. Show reagents that you could use to prepare the following ether via a Williamson ether synthesis and explain your reasoning.
please answer these questions. thanks
1. Write a reaction of the Williamson Ether synthesis of your product. 2. In this acid catalyzed reaction, a stable benzylic carbocation is formed. Show how this carbocation is formed. 3. Write resonance forms for the benzylic carbocation that is formed. 4. Use the government website www.uspto.gov to find the patent number for the synthesis of your product. Step 2: Ether Synthesis он OR NaBH ROH Amberlyst-15 NaoH H,O он он он
please answer question number
Questions: 1. Show, by equations, how you would prepare phenylbenzyl ether by the familiar Williamson synthesis. 2. In the preparation of methyl-2-napthoxy ether: A. What substances are present after the final reflux period? B. What serves as the nucleophile? C. How is the product purified? 3. In your preparation of 2,4-dinitrophenyl-p-tolylamine: In A. How is excess amine removed from the product? B. What serves as the nucleophile?
Please explain the folllwing thoroughly. Pictures will help! Thank
you very much.
increase in o ncrease in H2 CH2 -16, which would be the best way to carry out the following synthesis? OH Br a. (1) KOH, C2HsOH; (2) BH3:THF, then H202, OH b. (1) (CHb)aCOK/(CHs)jbCOH: (2) Ha0, then H20, heat c. (1) HA, heat; (2) H30*, H2O, heat d. (1) (CHa)sCOK/(CHs) COH; (2) BHs:THF, then H202, OH e. (1) KOH, C2HsOH: (2) HA, heat; (3) H30*, H2O, heat -17....
please explain how you got your answer, i am completely lost
Use synthetic division to determine whether iis a zero of the function. Show all work to receive credit. Give a reason for your answer. (2 points) f(x) = x4 - 2x3 + 4x2 - 2x + 3 Zero? e synthetic division and the remainder theorem to find the zeros of the function. Sh
Please explain clearly how they
got the answer, thank you!
Please explain clearly how they got the answer, thank you! A proton is accelerated from rest through a potential difference of 2.5 kV and then moves perpendicularly through a uniform 0.60-T magnetic field. What is the radius of the resulting path?
Can you please explain how you got your answer? Thank you!
For each of the following compounds, determine whether or not you would expect its IR spectrum to exhibit a signal to the left of 3000 cm1: Yes, we expect a signal above 3000 cm-1. O No, we do not expect a signal above 3000 cm-1. Yes, we expect a signal above 3000 cm-1. No, we do not expect a signal above 3000 cm-1. Yes, we expect a signal above...
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