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6. Predict the product and draw a mechanism for the reactions below. You MUST include the...
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...
6. Propose a mechanism and predict the product for the following reaction. Be sure to include...
6. Propose a mechanism and predict the product for the following reaction. Be sure to include resonance structures. (10 points) OCH AICI, 10 7. Provide the products for the following reactions (12 points) Bra. fuming FeBry H2SO4 AICI
2. (12 points, 6 points each) Give the arrow pushing mechanism for To of the following...
2. (12 points, 6 points each) Give the arrow pushing mechanism for To of the following reactions. Draw the resonance structures of the intermediate. You MUST include the mechanism for the formation of the electrophile for electrophilic substitution reactions. Do not combine steps and be sure to show arrows and charges for all steps. Gie Twoyo.coc.c.m.m.ci.e groded..ay are wotcleurly marked hwiti only gade wor A. HNO, H,So B. 1. AICI 2. H2o C. OzN NO2 NaOCH2CH 02N. heat N/A D....
Question 3. Predict the major products of the reactions below. Draw the full mechanism for the...
Question 3. Predict the major products of the reactions below. Draw the full mechanism for the reactions, using appropriate arrows to indicate electron movement and the full structures of any intermediate(s). Use the mechanism of the reaction to provide a rationale for why the major product formed. OM (1 equivalent) ansole Bry Febr (1 culle brambenzone Fer (1 equivalent Priloromethylbenzene (9 marks) Question 4. Predict the major product from the treatment of 2,5-dibromopyridine with ammonia. Draw the full mechanism for...
Problem 2 Use curved arrows to show mechanisms for both of the following reactions; the second...
Problem 2 Use curved arrows to show mechanisms for both of the following reactions; the second reaction produces a single product. Predict the structure of product A using your mechanism. In order to explain the regioselectivity in the formation of product A, include a detailed resonance analysis of the mechanism (i.e. show all resonance forms of the carbocation that contribute to the selectivity). Please also explain the observed selectivity in a few sentences. Bn z AICI:
Problem 5 Use curved arrows to show mechanisms for both of the following reactions; the second...
Problem 5 Use curved arrows to show mechanisms for both of the following reactions; the second reaction produces a single product. Predict the structure of product A using your mechanism. In order to explain the regioselectivity in the formation of product A, include a detailed resonance analysis of the mechanism (i.e. show all resonance forms of the carbocation that contribute to the selectivity). Please also explain the observed selectivity in a few sentences. i-PrSNa HNO3 H2SO4
4 and 5 PLEASE HELP curved arrows to indicate electron movement for each step. Draw all...
4 and 5 PLEASE HELP
curved arrows to indicate electron movement for each step. Draw all the resonance structures of the sigma complex intermediate. 4. (6 pts) a) Draw the complete mechanism to account for the following reaction. Make sure to show OCH3 Ords CI AICI 5. (6 pts) Draw the step-by-step mechanism for the reaction below, using curved arrows to show the flow of electrons and draw any resonance intermediates. Br Bг NO2 HNO3 H2SO4
are these correct? if not, can you explain? thanks! 9. a) Draw the mechanism for formation...
are these correct? if not, can
you explain? thanks!
9. a) Draw the mechanism for formation of the product shown. b) Draw the three resonance structures for the cation intermediate. (6 points total) HO-NO2 H2SO4 NO2 A mechanism: H-O-NO2 + H₂SO4 a H-O No2 t B) Resonance structures H NO2 H NO₂
please help Draw the mechanism for the transformation below. Be sure to draw all resonance structures...
please help
Draw the mechanism for the transformation below. Be sure to draw all resonance structures of the carbocation intermediate. Above the reaction arrow write 1.2-addition or 1.4 addition. Below the reaction arrow, wnte at wa temperature was this reaction conducted. Draw the mechanism for the transformation below. Be sure to draw all resonance structures of the carbocation intermediate. Above the reaction arrow write 1,2-addition or 1,4 addition. Below the reaction arrow, write at what temperature was this reaction conducted
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....
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...
6. Propose a mechanism and predict the product for the following reaction. Be sure to include resonance structures. (10 points) OCH AICI, 10 7. Provide the products for the following reactions (12 points) Bra. fuming FeBry H2SO4 AICI
2. (12 points, 6 points each) Give the arrow pushing mechanism for To of the following reactions. Draw the resonance structures of the intermediate. You MUST include the mechanism for the formation of the electrophile for electrophilic substitution reactions. Do not combine steps and be sure to show arrows and charges for all steps. Gie Twoyo.coc.c.m.m.ci.e groded..ay are wotcleurly marked hwiti only gade wor A. HNO, H,So B. 1. AICI 2. H2o C. OzN NO2 NaOCH2CH 02N. heat N/A D....
Question 3. Predict the major products of the reactions below. Draw the full mechanism for the reactions, using appropriate arrows to indicate electron movement and the full structures of any intermediate(s). Use the mechanism of the reaction to provide a rationale for why the major product formed. OM (1 equivalent) ansole Bry Febr (1 culle brambenzone Fer (1 equivalent Priloromethylbenzene (9 marks) Question 4. Predict the major product from the treatment of 2,5-dibromopyridine with ammonia. Draw the full mechanism for...
Problem 2 Use curved arrows to show mechanisms for both of the following reactions; the second reaction produces a single product. Predict the structure of product A using your mechanism. In order to explain the regioselectivity in the formation of product A, include a detailed resonance analysis of the mechanism (i.e. show all resonance forms of the carbocation that contribute to the selectivity). Please also explain the observed selectivity in a few sentences. Bn z AICI:
Problem 5 Use curved arrows to show mechanisms for both of the following reactions; the second reaction produces a single product. Predict the structure of product A using your mechanism. In order to explain the regioselectivity in the formation of product A, include a detailed resonance analysis of the mechanism (i.e. show all resonance forms of the carbocation that contribute to the selectivity). Please also explain the observed selectivity in a few sentences. i-PrSNa HNO3 H2SO4
4 and 5 PLEASE HELP
curved arrows to indicate electron movement for each step. Draw all the resonance structures of the sigma complex intermediate. 4. (6 pts) a) Draw the complete mechanism to account for the following reaction. Make sure to show OCH3 Ords CI AICI 5. (6 pts) Draw the step-by-step mechanism for the reaction below, using curved arrows to show the flow of electrons and draw any resonance intermediates. Br Bг NO2 HNO3 H2SO4
are these correct? if not, can
you explain? thanks!
9. a) Draw the mechanism for formation of the product shown. b) Draw the three resonance structures for the cation intermediate. (6 points total) HO-NO2 H2SO4 NO2 A mechanism: H-O-NO2 + H₂SO4 a H-O No2 t B) Resonance structures H NO2 H NO₂
please help
Draw the mechanism for the transformation below. Be sure to draw all resonance structures of the carbocation intermediate. Above the reaction arrow write 1.2-addition or 1.4 addition. Below the reaction arrow, wnte at wa temperature was this reaction conducted. Draw the mechanism for the transformation below. Be sure to draw all resonance structures of the carbocation intermediate. Above the reaction arrow write 1,2-addition or 1,4 addition. Below the reaction arrow, write at what temperature was this reaction conducted
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....
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