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C-0-C 1.76 8 (multiplet, 1H) Suggest structures for the following compounds that are consistent with the following formulas and 'H NMR data (multiplicity and relative peak integration). Where appropriate, IR data is given. are there Bshould ther Cntlanta "Cyttla Chem Shift 2.60 6 (septet, 1H)→isopropyl 2.10 8 (singlet, 3H) (doublet, 6H) → ISopropy! strong, sharp IR peak at 1716 cm 10-6=4 =a (combool e bond rings a) CSH100 missing aH 1.108 cither à Cng or doible bend Dlea, carbony 1716 $ bench on, todpleadumultiplicity triplet apt quartet 3pt b) C4H100 3.92 8 (singlet, 1H) 3.38 8 (doublet, 2H) r -0-C 1.76 8 (multiplet, 1H) ether 0.90 8 (doublet, 6H) -0H Sipt

C-0-C 1.76 8 (multiplet, 1H) Suggest structures for the following compounds that are consistent with the following formulas and 'H NMR data (multiplicity and relative peak integration). Where appropriate, IR data is given. are there Bshould ther Cntlanta "Cyttla Chem Shift 2.60 6 (septet, 1H)→isopropyl 2.10 8 (singlet, 3H) (doublet, 6H) → ISopropy! strong, sharp IR peak at 1716 cm 10-6=4 =a (combool e bond rings a) CSH100 missing aH 1.108 cither à Cng or doible bend Dlea, carbony 1716 $ bench on, todpleadumultiplicity triplet apt quartet 3pt b) C4H100 3.92 8 (singlet, 1H) 3.38 8 (doublet, 2H) r -0-C 1.76 8 (multiplet, 1H) ether 0.90 8 (doublet, 6H) -0H Sipt

Chemistry
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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15.57 Cntlania bosed an C fig, out how marg 4. Suggest structures for the following compounds that are consistent with the following H formulas and 'H NMR data (multiplicity and relative peak integration). Where are theme Bshould be appropriate, IR data is given. Cntlanta there Chem Shift 2.60 (septet, 1H)→ Isopropy! 2.10 8 (singlet, 3H) missing aH 1.10 8 (doublet, 6H) → 1Soprepy! strong, sharp IR peak at 1716 cm "Cyftla l0-6-니 =a (camboof Pi e bonds 3 a) CSH100 either à Cng or doubte bend Pa, carbony ac IH 30 ,CamltFell $ bench on, E, triplet apt quartet 3pt b) C4H100 3.92 8 (singlet, 1H) 3.38 8 (doublet, 2H) -0H -0-C 1.76 8 (multiplet, 1H) ether 0.90 8 (doublet, 6H) Sipt c) C12H18 2.50 8 (singlet) halogen rephtes suhnt happened to other d) C9H1|Br 7.22 8 (singlet, 5H) 3.38 8 (triplet, 2H) look For 2.75 8 (triplet, 2H) benzene 2.15 ô (quintet, 2H) Ting - look o NMR Snonls >7 benieane ring
Transcribed Image Text:15.57 Cntlania bosed an C fig, out how marg 4. Suggest structures for the following compounds that are consistent with the following H formulas and 'H NMR data (multiplicity and relative peak integration). Where are theme Bshould be appropriate, IR data is given. Cntlanta there Chem Shift 2.60 (septet, 1H)→ Isopropy! 2.10 8 (singlet, 3H) missing aH 1.10 8 (doublet, 6H) → 1Soprepy! strong, sharp IR peak at 1716 cm "Cyftla l0-6-니 =a (camboof Pi e bonds 3 a) CSH100 either à Cng or doubte bend Pa, carbony ac IH 30 ,CamltFell $ bench on, E, triplet apt quartet 3pt b) C4H100 3.92 8 (singlet, 1H) 3.38 8 (doublet, 2H) -0H -0-C 1.76 8 (multiplet, 1H) ether 0.90 8 (doublet, 6H) Sipt c) C12H18 2.50 8 (singlet) halogen rephtes suhnt happened to other d) C9H1|Br 7.22 8 (singlet, 5H) 3.38 8 (triplet, 2H) look For 2.75 8 (triplet, 2H) benzene 2.15 ô (quintet, 2H) Ting - look o NMR Snonls >7 benieane ring
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