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Deduce the structure of the compound that gives the following
Figure 9.43 The
Figure 9.44 A simulated broadband proton-decoupled
Figure 9.45 The IR spectrum for Problem 9.41. (SDBS, National Institute of Advanced Industrial Science and Technology)
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- Predict the structure of the compound using the information below. Kindly show what information are obtained for each spectra which may help in predicting the structure. From IR Spectra: See the attached picture From Mass Spectra M+ = 87 From Proton and Carbon NMR Spectra See attached picture.arrow_forwardBelow are the ¹H NMR spectrum of triphenylmethanol, benzophenone, and bromobenzene. Identify the compound corresponding to each ¹H NMR spectrum and draw the structure next to the ¹H NMR spectrum. Assign ALL peaks in each of the three ¹H NMR spectra. Hint: Conjugated systems (benzophenone) including an electronegative atom will cause a more downfield shift of ring protons in ¹H NMR compared with non-conjugated systems (bromobenzene). 8 8 8 7 7 7 6 6 6 5 5 5 4 PPM 4 PPM 4 PPM 3 3 3 2 2 2 1 1 1 0 0 0arrow_forwardHow many peaks would appear in the ¹3C NMR spectrum of this compound?arrow_forward
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- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning
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