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please place directly on where it's going so I don't get confused. Thanks uestion 17 Y...
please place directly on where it's going so I don't get
confused. Thanks
uestion 17 Y Catus: 10. 13 14 15. 16 1:20 PM u may attempt this question 3 more times uestion 8.60 for credit CО-Cна СО-CHн Hg(OAc)2 AcOHg- raw curved arrows to indicate teh flow of electrons in this step of teh mechanism for teh above reaction. CO2CH3 CO2CH3 Reset Arrows Аcонg Hg AcO Click the Help link on the upper right for drawing instructions. You may need...
Draw curved arrows to show electron reorganization during the following reaction. Click the Help link on...
Draw curved arrows to show electron reorganization during the following reaction. Click the Help link on the upper right for drawing instructions. You may need to scroll to the right to see the link. Reset Arrows :ÖH :o: H3C-0-0-H — H3C-C=CH2 HC—c=cH2 + + -H -I Make the ends of your curved arrows specify the destination of the reorganizing electron pair as precisely as possible. correct correct ✓ CHz H2Cc+ -H Hei: - H* + :C: CH3 incorrect incorrect H*...
CH3 CH3 1. Hg(OAC), H20 2. NaBH НО, І CH3 CH, Hoc H₃C/ Acid-catalyzed addition of...
CH3 CH3 1. Hg(OAC), H20 2. NaBH НО, І CH3 CH, Hoc H₃C/ Acid-catalyzed addition of water to an alkene yields an alcohol with Markovnikov regiochemistry. The electrophilic H adds to the sp carbon with the most hydrogens to yield the most stable carbocation intermediate, which then adds water to give the product alcohol. Because a carbocation intermediate is formed, rearrangements can occur prior to the addition of water. To avoid the possibility of rearrangement and still give a Markovnikov...
1. Hg(OAc)2, H20 2. NaBHA CH3 M HC CHE нас Acid-catalyzed addition of water to an...
1. Hg(OAc)2, H20 2. NaBHA CH3 M HC CHE нас Acid-catalyzed addition of water to an alkene yields an alcohol with Markovnikov regiochemistry. The electrophilic H adds to the sp carbon with the most hydrogens to yield the most stable carbocation intermediate, which then adds water to give the product alcohol. Because a carbocation intermediate is formed, rearrangements can occur prior to the addition of water To avoid the possibility of rearrangement and still give a Markovnikov alcohol, alkenes can...
2 problems 1. Hg(OAC)2, H20 2. NaBHg CH3 H3C H₃C Acid-catalyzed addition of water to an...
2
problems
1. Hg(OAC)2, H20 2. NaBHg CH3 H3C H₃C Acid-catalyzed addition of water to an alkene yields an alcohol with Markovnikov regiochemistry. The electrophilic add carbon with the most hydrogens to yield the most stable carbocation intermediate, which then adds water to give the produc Because a carbocation intermediate is formed, rearrangements can occur prior to the addition of water. To avoid the possibility of rearrangement and still give a Markovnikov alcohol, alkenes can instead be treated with mercury...
please help me with Organic Chemistry/Alkenes problems. Thank you! Directions: Place your answers to the following...
please help me with Organic Chemistry/Alkenes problems. Thank you!
Directions: Place your answers to the following questions in the spaces provided. 1. A common problem in the acid-catalyzed hydration of alkenes is the formation of an ether byproduct. Show the formation of the ether byproduct in relation to the reaction below by providing a curved-arrow mechanism for its formation. (2 pts) H30+ Н,0 OH Ans. 2. Which is the correct sequence of steps necessary to complete the following reaction? он...
[Re OCH3 OCH3 HBr The above reaction proceeds to yield only a single product. Draw the...
[Re OCH3 OCH3 HBr The above reaction proceeds to yield only a single product. Draw the structure(s) of the carbocation intermediate, including resonance contributors, to show why this is the case. . You do not have to consider stereochemistry . Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. . Separate resonance structures using the symbol from the drop-down menu. . . A (CH12; reacts with 1 molar equivalent of H2 over...
please place directly on where it's going so I don't get
confused. Thanks
uestion 17 Y Catus: 10. 13 14 15. 16 1:20 PM u may attempt this question 3 more times uestion 8.60 for credit CО-Cна СО-CHн Hg(OAc)2 AcOHg- raw curved arrows to indicate teh flow of electrons in this step of teh mechanism for teh above reaction. CO2CH3 CO2CH3 Reset Arrows Аcонg Hg AcO Click the Help link on the upper right for drawing instructions. You may need...
Draw curved arrows to show electron reorganization during the following reaction. Click the Help link on the upper right for drawing instructions. You may need to scroll to the right to see the link. Reset Arrows :ÖH :o: H3C-0-0-H — H3C-C=CH2 HC—c=cH2 + + -H -I Make the ends of your curved arrows specify the destination of the reorganizing electron pair as precisely as possible. correct correct ✓ CHz H2Cc+ -H Hei: - H* + :C: CH3 incorrect incorrect H*...
CH3 CH3 1. Hg(OAC), H20 2. NaBH НО, І CH3 CH, Hoc H₃C/ Acid-catalyzed addition of water to an alkene yields an alcohol with Markovnikov regiochemistry. The electrophilic H adds to the sp carbon with the most hydrogens to yield the most stable carbocation intermediate, which then adds water to give the product alcohol. Because a carbocation intermediate is formed, rearrangements can occur prior to the addition of water. To avoid the possibility of rearrangement and still give a Markovnikov...
1. Hg(OAc)2, H20 2. NaBHA CH3 M HC CHE нас Acid-catalyzed addition of water to an alkene yields an alcohol with Markovnikov regiochemistry. The electrophilic H adds to the sp carbon with the most hydrogens to yield the most stable carbocation intermediate, which then adds water to give the product alcohol. Because a carbocation intermediate is formed, rearrangements can occur prior to the addition of water To avoid the possibility of rearrangement and still give a Markovnikov alcohol, alkenes can...
2
problems
1. Hg(OAC)2, H20 2. NaBHg CH3 H3C H₃C Acid-catalyzed addition of water to an alkene yields an alcohol with Markovnikov regiochemistry. The electrophilic add carbon with the most hydrogens to yield the most stable carbocation intermediate, which then adds water to give the produc Because a carbocation intermediate is formed, rearrangements can occur prior to the addition of water. To avoid the possibility of rearrangement and still give a Markovnikov alcohol, alkenes can instead be treated with mercury...
please help me with Organic Chemistry/Alkenes problems. Thank you!
Directions: Place your answers to the following questions in the spaces provided. 1. A common problem in the acid-catalyzed hydration of alkenes is the formation of an ether byproduct. Show the formation of the ether byproduct in relation to the reaction below by providing a curved-arrow mechanism for its formation. (2 pts) H30+ Н,0 OH Ans. 2. Which is the correct sequence of steps necessary to complete the following reaction? он...
[Re OCH3 OCH3 HBr The above reaction proceeds to yield only a single product. Draw the structure(s) of the carbocation intermediate, including resonance contributors, to show why this is the case. . You do not have to consider stereochemistry . Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. . Separate resonance structures using the symbol from the drop-down menu. . . A (CH12; reacts with 1 molar equivalent of H2 over...
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