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Need help with C and E please
ULIO draw the carbocation Additional Questions: (16 (a) Use...
please answer all parts of question 16. thanks! Additional Questions: (16. (a) Use curved arrows to...
please answer all parts of question 16. thanks!
Additional Questions: (16. (a) Use curved arrows to illustrate electron movement, and draw the carbocation intermediate first formed from the reaction of HBr and the alkene shown below B obol brott + HBr homme biznos a A Z orts dizza n bo ubongow Abnuomo o bobbs How sot basDH Mont Habib nodar EDS ano b) sot bbs Hobib noch olibo w E s trossos ou 10 W hold on n o bolo...
ASU important unanisWL before leaving class d draw the carbocation od the alkene shown below. ebo...
ASU important unanisWL before leaving class d draw the carbocation od the alkene shown below. ebo BroUDU 52 Additional Questions: 16. a) Use curved arrows to illustrate electron movement, and drawi intermediate first formed from the reaction of HBr and the alke Toro 15 OD 901 915 Molebo Br + HBr om ni + HBO B oobs 3 dezodos los bruogma of babbsalo D o no sol bbs Hmont Hori bib node Vods wens OV no bag o ubora 2010...
Additional Questions: 16) (a) Use curved arrows to illustrate electron movement, and draw the carbocation intermedi...
Additional Questions: 16) (a) Use curved arrows to illustrate electron movement, and draw the carbocation intermediate first formed from the reaction of HBr and the alkene shown below Webno sanir o noso ondo lobo Bron WOH + HBO I do! bizn09
Help on all parts of question 3 would be greatly appreciated! 3. Treating alkene "A" below...
Help on all parts of question 3 would be greatly
appreciated!
3. Treating alkene "A" below with HBr can lead to a number of products. "A" + H-Br A bunch of products. For real, hella products. 3.A. Label the stereocenters in compound "A" as R or S and label the alkene as E or Z. 3.B. Draw the curved arrow mechanism leading to the most stabilized carbo- cation intermediate. (don't do any rearrangements, just acid/base with the alkene) H-Br most...
Draw a structural formula for the major organic product of the following reaction:
Draw a structural formula for the major organic product of the following reaction:Electrophilic addition of HBr to alkenes yields a bromoalkane. The reaction begins with an attack on the hydrogen of the electrophilic HBr by the electrons of the double bond to give a carbocation. This step follows Markovnikov's rule with the electrophilic H atom adding to the sp2 carbon containing the most hydrogens, leading to the formation of the most stable carbocation (1° < 2° < 3°). If possible, a...
Draw a structural formula for the major organic product of the reaction shown.
Electrophilic addition of HBr to alkenes yields a bromoalkane. The reaction begins with an attack on the hydrogen of the electrophilic HBr by the electrons of the double bond to give a carbocation. This step follows Markovnikov's rule with the electrophilic H atom adding to the sp2 carbon containing the most hydrogens, leading to the formation of the most stable carbocation (1° < 2° < 3°). If possible, a 1,2-shift of either a neighboring hydride or methyl group can occur...
Draw curved arrows to show the movement of electrons in this step of the mechanism.
Acid-catalyzed addition of water to an alkene yields an alcohol with Markovnikov regiochemistry. The electrophilic H+ adds to the sp2 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 instead be treated with mercury(II) acetate in aqueous THF and then subsequently...
please answer all parts, thanks! 1. More substituted alkenes are more stable than less substituted alkenes....
please answer all parts, thanks!
1. More substituted alkenes are more stable than less substituted alkenes. Show the orbital overlap that helps to explain this observation. 2. Why is the heat of hydrogenation for an alkene exothermic? Analyze the bonds that are changing. AH = -30 kcal/mol Explain: + H2 3. Treating alkene "A" below with HBr can lead to a number of products. "A" SM + H-Br A bunch of products. For real, hella products. 3.A. Label the stereocenters...
need help with this part benzene carbocation intermediate DOES NOT Critical Thinking Questions 1. For Rxn...
need help with this part
benzene carbocation intermediate DOES NOT Critical Thinking Questions 1. For Rxn 1 (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1: Reaction Diagrams for Electrophilic Addition of HCI V.E. V.E. (Potential Energy) H-C1 H-C1 carbocation intermediate Reaction Progress (Rxn 2) Reaction Progress (Rxn 1) 2. Rxn 1 is slightly down-hill in terms of energy. Rxn 2 is very up-hill in terms...
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 answer all parts of question 16. thanks!
Additional Questions: (16. (a) Use curved arrows to illustrate electron movement, and draw the carbocation intermediate first formed from the reaction of HBr and the alkene shown below B obol brott + HBr homme biznos a A Z orts dizza n bo ubongow Abnuomo o bobbs How sot basDH Mont Habib nodar EDS ano b) sot bbs Hobib noch olibo w E s trossos ou 10 W hold on n o bolo...
ASU important unanisWL before leaving class d draw the carbocation od the alkene shown below. ebo BroUDU 52 Additional Questions: 16. a) Use curved arrows to illustrate electron movement, and drawi intermediate first formed from the reaction of HBr and the alke Toro 15 OD 901 915 Molebo Br + HBr om ni + HBO B oobs 3 dezodos los bruogma of babbsalo D o no sol bbs Hmont Hori bib node Vods wens OV no bag o ubora 2010...
Additional Questions: 16) (a) Use curved arrows to illustrate electron movement, and draw the carbocation intermediate first formed from the reaction of HBr and the alkene shown below Webno sanir o noso ondo lobo Bron WOH + HBO I do! bizn09
Help on all parts of question 3 would be greatly
appreciated!
3. Treating alkene "A" below with HBr can lead to a number of products. "A" + H-Br A bunch of products. For real, hella products. 3.A. Label the stereocenters in compound "A" as R or S and label the alkene as E or Z. 3.B. Draw the curved arrow mechanism leading to the most stabilized carbo- cation intermediate. (don't do any rearrangements, just acid/base with the alkene) H-Br most...
please answer all parts, thanks!
1. More substituted alkenes are more stable than less substituted alkenes. Show the orbital overlap that helps to explain this observation. 2. Why is the heat of hydrogenation for an alkene exothermic? Analyze the bonds that are changing. AH = -30 kcal/mol Explain: + H2 3. Treating alkene "A" below with HBr can lead to a number of products. "A" SM + H-Br A bunch of products. For real, hella products. 3.A. Label the stereocenters...
need help with this part
benzene carbocation intermediate DOES NOT Critical Thinking Questions 1. For Rxn 1 (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1: Reaction Diagrams for Electrophilic Addition of HCI V.E. V.E. (Potential Energy) H-C1 H-C1 carbocation intermediate Reaction Progress (Rxn 2) Reaction Progress (Rxn 1) 2. Rxn 1 is slightly down-hill in terms of energy. Rxn 2 is very up-hill in terms...
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...
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