3,) you have now eliminated one substitution site and should have two possible sites remaining. Provide a mechanismfor the formation of each of the two remaining products. You should include all possible. Resident structures for the caton intermediates. There should be four resident structures in each mechanism. You do not need to show the mechanismfor the formation of the electrify you may assume that only a single iodine will add to the ring.a.b.GOLDEST GAD SE 1029OHHOH02AB o 1o1 meiasdoorn woms bevis song of olds pelI+noboibong tombong10 to asiqisminoviowTill brisH₂O, EtOHnaut nobibba as gada tasest 30 noodt to toubong Input sdr lo notaxillarynI+bouborg on to ving di salmsibb or Oetshqoqs edt onimaob or atob MM O bax H seuzie.bazanoitecu dale19H₂O, EtOHlliw gan snated a no quorg lanoituut invellib.noimadue shamore siliqotools alHoib blaos tad aquosy Insoitonut oor za milline V.mobest ad not sila noistade sittlenoiraut dues bleno) nobedog ad to goitoolTint:nce the

The objective is to determine the substitution sites of the vallin compound. The aldehyde group is…

3,) you have now eliminated one substitution site and should have two possible sites remaining. Provide a mechanism for the formation of each of the two remaining products. You should include all possible. Resident structures for the cat on intermediates. There should be four resident structures in each mechanism. You do not need to show the mechanism. for the formation of the electrify.you may assume that only a single iodine will add to the ring. a. b. OH H OH O2A sol maindoom wars bars I+ noboibog tombong diw glad of a to asiqismingulow H₂O, EtOH Jennut nobibbe as gode Masgests jo noiton si to tubong lapt sit lo mollasi I+ bubong and to ying sdi onlasib or 3.IT mes oft animabb or ateb SIMMO bau H anoitesu dale19 H₂O, EtOH liw gan snud a no equory lenoirsaut inveftib.noimadue siemote pilingontools al H blaos tedt aquoty issoitonut osts and milline V noboast od not siia noisutdedue sib fenoizagut dass hieno coinbedue sd to goitool int: nee tha

3,) you have now eliminated one substitution site and should have two possible sites remaining. Provide a mechanism for the formation of each of the two remaining products. You should include all possible. Resident structures for the cat on intermediates. There should be four resident structures in each mechanism. You do not need to show the mechanism. for the formation of the electrify.you may assume that only a single iodine will add to the ring. a. b. OH H OH O2A sol maindoom wars bars I+ noboibog tombong diw glad of a to asiqismingulow H₂O, EtOH Jennut nobibbe as gode Masgests jo noiton si to tubong lapt sit lo mollasi I+ bubong and to ying sdi onlasib or 3.IT mes oft animabb or ateb SIMMO bau H anoitesu dale19 H₂O, EtOH liw gan snud a no equory lenoirsaut inveftib.noimadue siemote pilingontools al H blaos tedt aquoty issoitonut osts and milline V noboast od not siia noisutdedue sib fenoizagut dass hieno coinbedue sd to goitool int: nee tha

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Similar questions

1
Draw the full electron pushing mechanism for the reaction depicted including ALL intermediates (with lone pairs and formal charges). Clearly label the electrophile and nucleophile in each step where appropriate.
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1. In the following reactions, draw the curved arrows needed to compete the first step of the mechanism. In the carbocation, draw in the bond for the new hydrogen atom so you can clearly see what carbon it is attached to. a. H-Br b. H-CI C. d. H-Br + Br H-CI + +Br
Fill in the appropriate reagent or starting material in each of the following reactions.
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The oxymercuration or the demercuration of this compound will form what product? A. 1-methylcyclohexan-1-ol/-methyl-1-cyclohexanol B. 1-methylcyclohexan-2-ol/-methyl-2-cyclohexanol C. 1-methylcyclohexan-3-ol/-methyl-3-cyclohexanol
Using the diagram below, answer the ff. questions.1. What pattern of curved arrow pushing is the second step of this reaction?a. loss of a leaving groupb. proton transferc. rearrangement 2. What pattern of curved arrow pushing is the fourth step of this reaction?a. proton transferb. loss of a leaving groupc. nucleophilic attack
Draw the strcutres of the missing reactants, intermediates, or products in the following mechanisms. Include all lone pairs.
1. Fill in the necessary starting material, reactants or product for the reactions shown below. A. B. C. I. NaNH,, NH, 2. CH₂CH₂CH₂CH₂Cl 1. NaNH,, NH, 2. CH₂CH₂CI 2. Show the complete mechanism for A. and B. from above. Use the back if necessary.
6. Design a synthesis: ?? H₂N OCH2CH3