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7. Draw...
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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
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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).
7. Draw the major product expected in each reaction below. (10 pts) HAPO H₂C CH3 CH₃...
7. Draw the major product expected in each reaction below. (10 pts) HAPO H₂C CH3 CH₃ он heat CH2CH2ONa Hych ii. Br T TCH.CH, CH3CH2OH нэ 55 °C KSH (1 mol equivalent) acetonitrile он acetonitrile
Quickly show all steps and answers all parts of the question please thank you 5. Predict...
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5. Predict the eliminations products A and B formed (E-1 mechanism) when 4,4-dimethylhexan- 3-ol is heated with concentrated phosphoric acid. Also, identify the rate determining step and the major product using Zaitsev's Rule? (Mechanism must be shown to receive full points) (20 pts) он conc. H3PO4 CH3 Products A and B нас E-1 condition HzC CH3 4,4-dimethylhexan-3-ol
6&7 please 6. For the following reactions tell whether they will react under Secondition condition (Nal/acetone)...
6&7 please
6. For the following reactions tell whether they will react under Secondition condition (Nal/acetone) or neither. Also indicate the product formed if any (10 points Mechanism Product (S.1 or 2) my НАС " H₂C CHO 7. Draw the major product expected in each reaction below. (10 pts) HAPO. HC CH3 heat OH CH3CH ONa нсін CH,CH OH 55°C B CH2CH3 KSH (1 mol equivalent) acetonitrile он acetonitrile
help with all of these ! Question 8: Which is the better retrosynthesis for the given target molecule? Explain and...
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Question 8: Which is the better retrosynthesis for the given target molecule? Explain and provide a one-step synthesis of the target molecule. Br Br Hас Hас Hас .CH3 b) NaQH CHy Question 7: Draw the plausible mechanism for each of the folllowing transformations: a) CHy Не нс CHs CH СH, CH3 conc. H,SO -CH3 heat CH он Question 5 Predict the major and minor products for the following reactions: a) NaSH Н,с b) Br...
answer all three questions and circle the answers Which of the following reactions will not produce...
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Which of the following reactions will not produce the major product given? Br CH3OH (racemic) OSO?CF3 NaBr acetone но н NaBr acetone Br CH3 H CH3 CH3CH2ONa HRCH H3C CH2CH3 CH2CH3 H11.8 - Level 1 Homework . Unanswered For the given reaction, predict the major and minor products. NaCN DMF Premise Response Drag and drop to match = A Major B Minor Unanswered - Submit H11.9 - Level 1 Homework. Unanswered For...
please answer all thank you so much Question 1 Which of the following mechanistic steps represents...
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Question 1 Which of the following mechanistic steps represents the loss of a leaving group? OH OH2 H Br II 18-05-4 IV AI B. II C. D.IV Question 3 What is product of the following reaction sequence? ОН 1. PCC 2. C2H5MgBr 3. Н* wоrkup ОН ОН ОН IV ОА І В. І С. ІІІ OD. IV Question 4 What is the major product formed in the following reaction? Br NaH A NH2...
please help in all sections!! Which of the following compounds is least reactive towards a nucleophilic...
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Which of the following compounds is least reactive towards a nucleophilic addition reaction? H H H IV II II1O V Provide the product for the following reaction. OH 1. NH2NH2/ H 2. КОНІН-О/Д 3. H30* NNH2 OH OH NNH2 NH2 OH II IV OH Eo- Provide the major product for the following reaction sequence 1. NH2NH2/ H 2. КОН/Н20/Д AICI3 II H2NN IV Predict the product for the following reaction. excess Нао н H2SO4 но...
please show all steps including each mechanism (arrows) and also if SN1 has any rearrangements of...
please show all steps including each mechanism (arrows) and
also if SN1 has any rearrangements of carbocation intermediate
through a hydride shift and/or methyl shift. DO NOT NEED
ELIMINATION. ONLY SUBSTITUTION.
Sy1/E1 versus S2/E2 Learning Checks Draw the major organic substitution and/or elimination products in the following reactions. If no reaction is possible, write “No Reaction". Substitution Product(s) Elimination Product(s) 2) 2) OH BrCH K* -Ot-Bu NaOCH н"Сн, сн,он нсн, Ph NaOCH Br H CH3OH CH NaOCH NaOH T.CH, I...
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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
Quickly show all steps and
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).
7. Draw the major product expected in each reaction below. (10 pts) HAPO H₂C CH3 CH₃ он heat CH2CH2ONa Hych ii. Br T TCH.CH, CH3CH2OH нэ 55 °C KSH (1 mol equivalent) acetonitrile он acetonitrile
Quickly show all steps and answers
all parts of the question please thank you
5. Predict the eliminations products A and B formed (E-1 mechanism) when 4,4-dimethylhexan- 3-ol is heated with concentrated phosphoric acid. Also, identify the rate determining step and the major product using Zaitsev's Rule? (Mechanism must be shown to receive full points) (20 pts) он conc. H3PO4 CH3 Products A and B нас E-1 condition HzC CH3 4,4-dimethylhexan-3-ol
6&7 please
6. For the following reactions tell whether they will react under Secondition condition (Nal/acetone) or neither. Also indicate the product formed if any (10 points Mechanism Product (S.1 or 2) my НАС " H₂C CHO 7. Draw the major product expected in each reaction below. (10 pts) HAPO. HC CH3 heat OH CH3CH ONa нсін CH,CH OH 55°C B CH2CH3 KSH (1 mol equivalent) acetonitrile он acetonitrile
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Question 8: Which is the better retrosynthesis for the given target molecule? Explain and provide a one-step synthesis of the target molecule. Br Br Hас Hас Hас .CH3 b) NaQH CHy Question 7: Draw the plausible mechanism for each of the folllowing transformations: a) CHy Не нс CHs CH СH, CH3 conc. H,SO -CH3 heat CH он Question 5 Predict the major and minor products for the following reactions: a) NaSH Н,с b) Br...
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Which of the following reactions will not produce the major product given? Br CH3OH (racemic) OSO?CF3 NaBr acetone но н NaBr acetone Br CH3 H CH3 CH3CH2ONa HRCH H3C CH2CH3 CH2CH3 H11.8 - Level 1 Homework . Unanswered For the given reaction, predict the major and minor products. NaCN DMF Premise Response Drag and drop to match = A Major B Minor Unanswered - Submit H11.9 - Level 1 Homework. Unanswered For...
please answer all thank you so much
Question 1 Which of the following mechanistic steps represents the loss of a leaving group? OH OH2 H Br II 18-05-4 IV AI B. II C. D.IV Question 3 What is product of the following reaction sequence? ОН 1. PCC 2. C2H5MgBr 3. Н* wоrkup ОН ОН ОН IV ОА І В. І С. ІІІ OD. IV Question 4 What is the major product formed in the following reaction? Br NaH A NH2...
please help in all sections!!
Which of the following compounds is least reactive towards a nucleophilic addition reaction? H H H IV II II1O V Provide the product for the following reaction. OH 1. NH2NH2/ H 2. КОНІН-О/Д 3. H30* NNH2 OH OH NNH2 NH2 OH II IV OH Eo- Provide the major product for the following reaction sequence 1. NH2NH2/ H 2. КОН/Н20/Д AICI3 II H2NN IV Predict the product for the following reaction. excess Нао н H2SO4 но...
please show all steps including each mechanism (arrows) and
also if SN1 has any rearrangements of carbocation intermediate
through a hydride shift and/or methyl shift. DO NOT NEED
ELIMINATION. ONLY SUBSTITUTION.
Sy1/E1 versus S2/E2 Learning Checks Draw the major organic substitution and/or elimination products in the following reactions. If no reaction is possible, write “No Reaction". Substitution Product(s) Elimination Product(s) 2) 2) OH BrCH K* -Ot-Bu NaOCH н"Сн, сн,он нсн, Ph NaOCH Br H CH3OH CH NaOCH NaOH T.CH, I...
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