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attempt 31. value 6.38 points You did not receive...
can you help me answer this question? 28. 6.38 points You did not receive full credit...
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28. 6.38 points You did not receive full credit for this question in a previous attempt Be sure to answer all parts. Draw two different ways to prepare (CH),CHCOC(CH), from an acid chloride and an organocuprate reagent. Be sure to draw the skeletal (line-bond) structures of each starting material: condensed structures will not be accepted. Part 1 out of 2 edit structure edit structure acid chloride organecuprate Report problem Check my work Next...
can you help me answer this question? 39. 6.38 points You did not receive full credit...
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39. 6.38 points You did not receive full credit for this question in a previous attempt Check my work Click the "draw structure" button to launch the drawing utility. Report problem Draw the organic product of the following Wittig reaction. Hint PhPa -O + draw structure References eBook & Resources Multipart Answer Difficulty: Medium
can you help me answer this question? 30. You did not receive full credit for this...
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30. You did not receive full credit for this question in a previous attempt 6.38 points Be sure to answer all parts. How can (CH),C-CHCOCH, (mesityl oxide) be converted to the following compound. Part 1 out of 2 1 X 12H20 edit structure... Select the correct reagent X. There may be more than one correct answer. | CH, CHMgBr (CH, CH) Culi CH-CHBr CH-CHLI Report problem Check my work Next part Hint
can you help me answer this? 13. 6.38 points You did not receive full credit for...
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13. 6.38 points You did not receive full credit for this question in a previous attempt Be sure to answer all parts. Draw one resonance structure for each of the conjugate bases formed by removal of the labeled protons (H ,H, and H) in cyclohexane-1,3-dione. Rank these protons in order of increasing acidity and explain the order you chose. dients. cyclohexane-1,3-dione Part 1 out of 3 out Mail dil Draw one resonance structure for...
can you help me answer this? 20. 6.38 points You did not receive full credit for this question in a previous attempt...
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20. 6.38 points You did not receive full credit for this question in a previous attempt Click the "draw structure" button to launch the drawing utility. Part 1 out of 2 What product is formed when the following compound is treated with ARO, NH,OH? 에 오 draw structure. Report problem Check my work Next part Hint
can you help me answer this question? Question 38 of 47) Submit 38. 6.38 points You...
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Question 38 of 47) Submit 38. 6.38 points You did not receive full credit for this question in a previous attempt Check my work Click the "draw structure" button to launch the drawing utility. Report problem What alkene would yield 2,2-dimethoxycyclopentane-1,3-dicarbaldehyde on treatment with O; followed by (CH),S? Hint 2,2-dimethoxycyclopentane-1,3-dicarbaldehyde edit structure
can you help me solve these 5 questions please? thank you :) 1.) 2.) 3.) 4.)...
can you help me solve these 5 questions please? thank you
:)
1.)
2.)
3.)
4.)
5.)
Give the major substitution product of the following reaction. Br CH3CO2H ? heat OH SCH O NH2 O o There is no reaction under these conditions or the correct product is not listed here. Give the major substitution product of the following reaction. Br CH3OH ? heat There is no reaction under these conditions or the correct product is not listed here. OH...
can you help me answer this question? < Question 35 of 47 - 35. 6.38 points...
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you help me answer this question?
< Question 35 of 47 - 35. 6.38 points You did not receive full credit for this question in a previous attempt Check my work Click the "draw structure button to launch the drawing utility. Report problem Use the 'H NMR and IR data to determine the structure of the following compound Hint Compound B Molecular formula CH,0 IR absorption at 1718 cm-" IH NMR data: 1.10 (doublet, 6 H), 2.14 (singlet, 3H),...
can you help me answer this question? 29. 338 points You did not receive full credit...
can
you help me answer this question?
29. 338 points You did not receive full credit for this question in a previous attempt Be sure to answer all parts. Part 1 out of 2 Draw the product when the compound shown above is treated with (CH),Cull, followed by H20. edit structure Report problem Check my work Next part Hint
If you could help me with each question and give me a brief explantion, its all...
If you could help me with each question and give me a brief
explantion, its all that I have left to do on my homework, thanks
so much :)
7) Give a complete plausible mechanism for the radical chlorination of the compound to give the product shown: (Show the initiation, propagation, and termination steps.) Cl ses fr e racti sho1) Give the reagents needed to accomplish the following reactions ·w rite you answers on the paper provided for each question!...
can you help me answer this question?
28. 6.38 points You did not receive full credit for this question in a previous attempt Be sure to answer all parts. Draw two different ways to prepare (CH),CHCOC(CH), from an acid chloride and an organocuprate reagent. Be sure to draw the skeletal (line-bond) structures of each starting material: condensed structures will not be accepted. Part 1 out of 2 edit structure edit structure acid chloride organecuprate Report problem Check my work Next...
can you help me answer this question?
39. 6.38 points You did not receive full credit for this question in a previous attempt Check my work Click the "draw structure" button to launch the drawing utility. Report problem Draw the organic product of the following Wittig reaction. Hint PhPa -O + draw structure References eBook & Resources Multipart Answer Difficulty: Medium
can
you help me answer this question?
30. You did not receive full credit for this question in a previous attempt 6.38 points Be sure to answer all parts. How can (CH),C-CHCOCH, (mesityl oxide) be converted to the following compound. Part 1 out of 2 1 X 12H20 edit structure... Select the correct reagent X. There may be more than one correct answer. | CH, CHMgBr (CH, CH) Culi CH-CHBr CH-CHLI Report problem Check my work Next part Hint
can you help me answer this?
13. 6.38 points You did not receive full credit for this question in a previous attempt Be sure to answer all parts. Draw one resonance structure for each of the conjugate bases formed by removal of the labeled protons (H ,H, and H) in cyclohexane-1,3-dione. Rank these protons in order of increasing acidity and explain the order you chose. dients. cyclohexane-1,3-dione Part 1 out of 3 out Mail dil Draw one resonance structure for...
can you help me answer this?
20. 6.38 points You did not receive full credit for this question in a previous attempt Click the "draw structure" button to launch the drawing utility. Part 1 out of 2 What product is formed when the following compound is treated with ARO, NH,OH? 에 오 draw structure. Report problem Check my work Next part Hint
can you help me answer this question?
Question 38 of 47) Submit 38. 6.38 points You did not receive full credit for this question in a previous attempt Check my work Click the "draw structure" button to launch the drawing utility. Report problem What alkene would yield 2,2-dimethoxycyclopentane-1,3-dicarbaldehyde on treatment with O; followed by (CH),S? Hint 2,2-dimethoxycyclopentane-1,3-dicarbaldehyde edit structure
can you help me solve these 5 questions please? thank you
:)
1.)
2.)
3.)
4.)
5.)
Give the major substitution product of the following reaction. Br CH3CO2H ? heat OH SCH O NH2 O o There is no reaction under these conditions or the correct product is not listed here. Give the major substitution product of the following reaction. Br CH3OH ? heat There is no reaction under these conditions or the correct product is not listed here. OH...
can
you help me answer this question?
< Question 35 of 47 - 35. 6.38 points You did not receive full credit for this question in a previous attempt Check my work Click the "draw structure button to launch the drawing utility. Report problem Use the 'H NMR and IR data to determine the structure of the following compound Hint Compound B Molecular formula CH,0 IR absorption at 1718 cm-" IH NMR data: 1.10 (doublet, 6 H), 2.14 (singlet, 3H),...
can
you help me answer this question?
29. 338 points You did not receive full credit for this question in a previous attempt Be sure to answer all parts. Part 1 out of 2 Draw the product when the compound shown above is treated with (CH),Cull, followed by H20. edit structure Report problem Check my work Next part Hint
If you could help me with each question and give me a brief
explantion, its all that I have left to do on my homework, thanks
so much :)
7) Give a complete plausible mechanism for the radical chlorination of the compound to give the product shown: (Show the initiation, propagation, and termination steps.) Cl ses fr e racti sho1) Give the reagents needed to accomplish the following reactions ·w rite you answers on the paper provided for each question!...
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