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The given reaction is followed by electrophilic aromatic
substitution reaction in this one ketone act as meta directing
groups 
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2. Considering the effect of the substituent on the...
Name: 3 1. Assuming each compound is planar, state which of the following compounds are aromatic...
Name: 3 1. Assuming each compound is planar, state which of the following compounds are aromatic and for each say why (8 points). a. b. d. C. HON b) Using curved arrows show how two more resonance structure can be derived for the following (show the derived structure). (2 points) d 2. Considering the effect of the substituent on the benzene ring below. Identify the major product of the following reaction. (20 points) a. (5 points) Hat Аневи Br2 FeBr3...
Name: Assuming each compound is planar, state which of the following compounds are aromatic for each...
Name: Assuming each compound is planar, state which of the following compounds are aromatic for each say why (8 points) b) Using curved arrows show how two more resonance structure can be derived for the following (show the derived structure). (2 points) 2. Considering the effect of the substituent on the benzene ring below. Identify the major product of the following reaction. (20 points) a. (5 points) Br2 FeBrg b. What is the active Electrophile for this reaction? (3 points)...
Draw the mechanism of the following reaction. Be sure to show all curved arrows and formal...
Draw the mechanism of the following reaction. Be sure to show all curved arrows and formal charges. (Show the formation of the electrophile and all resonance structures of the sigma complex). o to AICI: Does the substituent on the following benzene activate or deactivate the ring for EAS reactions? Explain your answer this should include drawing any relevant resonance structures!) NH Predict the major product of the following reaction. Explain the directing effects of the -OH group (this should include...
all three questions Application Questions 1. Draw the mechanism for the sulfonation of benzene. Use HSO...
all three questions
Application Questions 1. Draw the mechanism for the sulfonation of benzene. Use HSO as the electrophile. Draw the all the resonance structures of the stabilized cation intermediate 2. Draw the major product formed when each of the following compounds is treated with Cly/AICI, Assume chlorination only occurs in one position on the ring rather than multiple positions. COM COCX ooo 3. Predict whether toluene or chlorobenzene would undergo electrophilic aromatic substitution more quickly when treated with C1z/AICI....
1. please check what is wrong. Thank you! Determine the product formed when each compound is treated with...
1. please check what is wrong. Thank you!
Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...
1. For the following compounds, label each substituent as electron donating or electron withdrawing, and indicate...
1. For the following compounds, label each substituent as electron donating or electron withdrawing, and indicate whether this effect is achieved via induction or resonance. ŅO2 H2N SO3H 2. Predict the TH NMR of the above benzene derivatives. For chemical shift, indicate whether the peak would likely be downfield or upfield of benzene (7.2 ppm). (Hint: think about the resonance structures that can be drawn based on your responses from above) A B # of peaks chemical shift indicate: >7.2,...
help Thank you 4. (10 pts) Draw all possible products for the following reaction including stereoisomers....
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4. (10 pts) Draw all possible products for the following reaction including stereoisomers. Note that the addition occurs through a "syn" mechanism. Is the product solution optically active (yes or no)? 1. BAHATHF 2. NaOH, HO (8 pts) Provide a complete mechanism for the reaction below and include lone-pairs of electrons and formal charges. Show all products formed including stereoisomers. Is the product solution optically active (yes or no)? Bras 11. (8 pts) Draw all four regiochemical...
Quickly show all steps and answers all parts of the question please thank you 3. In...
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answers all parts of the question please thank you
3. In the deuterium-labeled compound below predict the product(s) of the elimination reaction of the following elimination reaction and tell whether the alkene formed contains deuterium or not. (20 pts) HCCH; OH H2SO4(aq) heat н,с (ii) NaOCH.CH CH,CH,OH heat CH3 (iii) Write a detail mechanism for the formation of the product in question 3(i).
1) Provide a detailed electron pushing mechanism for the below transformation. Show ALL relevant resonance structures...
1) Provide a detailed electron pushing mechanism for the below transformation. Show ALL relevant resonance structures to help explain why the para product is the major organic product. (Note: your electron pushing mechanism should include formation of the electrophile) (4 points) Cl AICl3
Quickly show all steps and answers all parts of the question please thank you 2. Show...
Quickly show all steps and answers all parts of the question
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2. Show the step by step mechanism to account for the following transformation. Also predict the major product formed. (20 points) CH3 OH conc. HBO CH₂ H₂CX Br CH₂ H3C CHE H₃C CH Swi condition Br L CH3 CH3 H₃C HC X X
Name: 3 1. Assuming each compound is planar, state which of the following compounds are aromatic and for each say why (8 points). a. b. d. C. HON b) Using curved arrows show how two more resonance structure can be derived for the following (show the derived structure). (2 points) d 2. Considering the effect of the substituent on the benzene ring below. Identify the major product of the following reaction. (20 points) a. (5 points) Hat Аневи Br2 FeBr3...
Name: Assuming each compound is planar, state which of the following compounds are aromatic for each say why (8 points) b) Using curved arrows show how two more resonance structure can be derived for the following (show the derived structure). (2 points) 2. Considering the effect of the substituent on the benzene ring below. Identify the major product of the following reaction. (20 points) a. (5 points) Br2 FeBrg b. What is the active Electrophile for this reaction? (3 points)...
Draw the mechanism of the following reaction. Be sure to show all curved arrows and formal charges. (Show the formation of the electrophile and all resonance structures of the sigma complex). o to AICI: Does the substituent on the following benzene activate or deactivate the ring for EAS reactions? Explain your answer this should include drawing any relevant resonance structures!) NH Predict the major product of the following reaction. Explain the directing effects of the -OH group (this should include...
all three questions
Application Questions 1. Draw the mechanism for the sulfonation of benzene. Use HSO as the electrophile. Draw the all the resonance structures of the stabilized cation intermediate 2. Draw the major product formed when each of the following compounds is treated with Cly/AICI, Assume chlorination only occurs in one position on the ring rather than multiple positions. COM COCX ooo 3. Predict whether toluene or chlorobenzene would undergo electrophilic aromatic substitution more quickly when treated with C1z/AICI....
1. please check what is wrong. Thank you!
Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...
1. For the following compounds, label each substituent as electron donating or electron withdrawing, and indicate whether this effect is achieved via induction or resonance. ŅO2 H2N SO3H 2. Predict the TH NMR of the above benzene derivatives. For chemical shift, indicate whether the peak would likely be downfield or upfield of benzene (7.2 ppm). (Hint: think about the resonance structures that can be drawn based on your responses from above) A B # of peaks chemical shift indicate: >7.2,...
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4. (10 pts) Draw all possible products for the following reaction including stereoisomers. Note that the addition occurs through a "syn" mechanism. Is the product solution optically active (yes or no)? 1. BAHATHF 2. NaOH, HO (8 pts) Provide a complete mechanism for the reaction below and include lone-pairs of electrons and formal charges. Show all products formed including stereoisomers. Is the product solution optically active (yes or no)? Bras 11. (8 pts) Draw all four regiochemical...
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answers all parts of the question please thank you
3. In the deuterium-labeled compound below predict the product(s) of the elimination reaction of the following elimination reaction and tell whether the alkene formed contains deuterium or not. (20 pts) HCCH; OH H2SO4(aq) heat н,с (ii) NaOCH.CH CH,CH,OH heat CH3 (iii) Write a detail mechanism for the formation of the product in question 3(i).
1) Provide a detailed electron pushing mechanism for the below transformation. Show ALL relevant resonance structures to help explain why the para product is the major organic product. (Note: your electron pushing mechanism should include formation of the electrophile) (4 points) Cl AICl3
Quickly show all steps and answers all parts of the question
please thank you
2. Show the step by step mechanism to account for the following transformation. Also predict the major product formed. (20 points) CH3 OH conc. HBO CH₂ H₂CX Br CH₂ H3C CHE H₃C CH Swi condition Br L CH3 CH3 H₃C HC X X
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