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1) Draw the mechanism for the radical reaction below, including potential resonance structures that explain the...
[8 marks] 1. In the boxes below, draw the resonance structures of the organic radical intermediate...
[8 marks] 1. In the boxes below, draw the resonance structures of the organic radical intermediate of the given reaction, along with the two different products (constitutional isomers) that would be produced. No electron-flow arrows are required at any time. Stereochemistry is not required. Note: NBS N-bromosuccinimide Organic reaction intermediate NBS hv Product 2 Product 1 [6 marks 2. In the boxes below, draw structures corresponding to the following names. Please use proper line-angle
Draw a complete mechanism (including resonance structures) for the monobromination of toluene using Br_2 and FeBr_s....
Draw a complete mechanism (including resonance structures) for the monobromination of toluene using Br_2 and FeBr_s. Assume the product has a para relationship between the bremo-and methyl-groups.
Draw the major product and write the complete mechanism for the following reaction. Show resonance structures...
Draw the major product and write the complete mechanism for the following reaction. Show resonance structures that lead to the formation of the major product.
1. Determine the mechanism of each nucleophilic substitution reaction and explain why? Draw the products including...
1. Determine the mechanism of each nucleophilic substitution reaction and explain why? Draw the products including the stereochemistry. (6 points) Br + CN acetone d. ~ + CH,CO2H - Y Y + POCHE UCH DMSO + TOCH.CH DMF b. + B + OCH + CH4OH DMSO – w ! ho + OCHCH , CH,CH,OH DM . Br + CH3OH + CH3CH,OH
8. Draw the structure of the major product afforded from the reaction conditions below in the...
8. Draw the structure of the major product afforded from the reaction conditions below in the box provided. (5 pts.) Ph3P: CBr4 OH 9. Provide a proper electron-pushing mechanism (including resonance structures) using curved arrows that describes the monochlorination of p-methyltoluene. (10 pts.) CI-CI + HCI hy p-methyltoluene CI:
Draw both expected products of the following reaction by augmenting the two structures given below.
Draw both expected products of the following reaction by
augmenting the two structures given below. If more than two
structures are possible, draw only the major products
expected.
Draw both expected products of the following reaction by augmenting the two structures given below. If more than two structures are possible, draw only the major products expected. HO H3C -C-CI NO2 AlCl3 click to edit HO NO2
Draw both expected products of the following reaction by augmenting the two structures given...
6. (4 pts.) Draw the two resonance structures of the enolate formed from the following reaction: 7. (4 pts) Draw th...
6. (4 pts.) Draw the two resonance structures of the enolate formed from the following reaction: 7. (4 pts) Draw the structure of an alkyl bromide (R-Br) and an alkoxide (R-O) that would provide the most efficient synthesis of the following ether by the Williamson ether synthesis. Target ether 8. (5 pts.) Draw a mechanism for the following E2 reaction. Draw the major product. Be sure to include any necessary H's in your structure as you draw the mechanism. OH...
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
Draw the mechanism for the following transformation. Include all relevant resonance structures. Show the movement of...
Draw the mechanism for the following transformation. Include all
relevant resonance structures. Show the movement of electrons with
arrows.
Draw the mechanism for the following transformation. Include all relevant resonance structures. Show the movement of electrons with arrows. (14 points) Pro excess HBr Br
Draw a plausible mechanism for the reaction shown below, being sure to show all intermediates, charges and resonance str...
Draw a plausible mechanism for the reaction shown below, being
sure to show all intermediates, charges and resonance
structures
4. Draw a plausible mechanism for the reaction shown below, being sure to show all intermediates, charges and resonance structures. (12 points) O CH3NH2O OH DCC
[8 marks] 1. In the boxes below, draw the resonance structures of the organic radical intermediate of the given reaction, along with the two different products (constitutional isomers) that would be produced. No electron-flow arrows are required at any time. Stereochemistry is not required. Note: NBS N-bromosuccinimide Organic reaction intermediate NBS hv Product 2 Product 1 [6 marks 2. In the boxes below, draw structures corresponding to the following names. Please use proper line-angle
Draw a complete mechanism (including resonance structures) for the monobromination of toluene using Br_2 and FeBr_s. Assume the product has a para relationship between the bremo-and methyl-groups.
Draw the major product and write the complete mechanism for the following reaction. Show resonance structures that lead to the formation of the major product.
1. Determine the mechanism of each nucleophilic substitution reaction and explain why? Draw the products including the stereochemistry. (6 points) Br + CN acetone d. ~ + CH,CO2H - Y Y + POCHE UCH DMSO + TOCH.CH DMF b. + B + OCH + CH4OH DMSO – w ! ho + OCHCH , CH,CH,OH DM . Br + CH3OH + CH3CH,OH
8. Draw the structure of the major product afforded from the reaction conditions below in the box provided. (5 pts.) Ph3P: CBr4 OH 9. Provide a proper electron-pushing mechanism (including resonance structures) using curved arrows that describes the monochlorination of p-methyltoluene. (10 pts.) CI-CI + HCI hy p-methyltoluene CI:
Draw both expected products of the following reaction by
augmenting the two structures given below. If more than two
structures are possible, draw only the major products
expected.
Draw both expected products of the following reaction by augmenting the two structures given below. If more than two structures are possible, draw only the major products expected. HO H3C -C-CI NO2 AlCl3 click to edit HO NO2
Draw both expected products of the following reaction by augmenting the two structures given...
6. (4 pts.) Draw the two resonance structures of the enolate formed from the following reaction: 7. (4 pts) Draw the structure of an alkyl bromide (R-Br) and an alkoxide (R-O) that would provide the most efficient synthesis of the following ether by the Williamson ether synthesis. Target ether 8. (5 pts.) Draw a mechanism for the following E2 reaction. Draw the major product. Be sure to include any necessary H's in your structure as you draw the mechanism. OH...
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
Draw the mechanism for the following transformation. Include all
relevant resonance structures. Show the movement of electrons with
arrows.
Draw the mechanism for the following transformation. Include all relevant resonance structures. Show the movement of electrons with arrows. (14 points) Pro excess HBr Br
Draw a plausible mechanism for the reaction shown below, being
sure to show all intermediates, charges and resonance
structures
4. Draw a plausible mechanism for the reaction shown below, being sure to show all intermediates, charges and resonance structures. (12 points) O CH3NH2O OH DCC
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