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Compound Z
Figure 6 The
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- Compound I (C11H14O2) is insoluble in water, aqueous acid, and aqueous NaHCO3, but dissolves readily in 10% Na2CO3 and 10% NaOH. When these alkaline solutions are acidified with 10% HCl, compound I is recovered unchanged. Given this information and its 1H-NMR spectrum, deduce the structure of compound I.arrow_forwardA solution of acetone [(CH3)2C=O] in ethanol (CH3CH2OH) in the presence of a trace of acid was allowed to stand for several days, and a new compound of molecular formula C7H16O2 was formed. The IR spectrum showed only one major peak in the functional group region around 3000 cm−1, and the 1H NMR spectrum is given here. What is the structure of the product?arrow_forwardGiven here are 1H-NMR and 13C-NMR spectral data for nine compounds. Each compound shows strong absorption between 1720 and 1700 cm-1 and strong, broad absorption over the region 2500–3300 cm-1. Propose a structural formula for each compound.arrow_forward
- Compound L has the formula C₁1H₁5 NO. The ¹H NMR, 13C NMR and the IR spectra for Compound L are shown below. Propose a structure for Compound L. 12 4800 11 HSP-01-587 DEPT-90 DEPT-135 1 : T T 10 9 200 2 2 CDS-06-337 8 7 180 160 6 : 140 5 ppm 120 4 4 3 100 : 6 ppm 2 T T 1 to maineriberent waiho mlenmol wons havus saonic 80 D 0 -1 T 60 40 20 4 T 0arrow_forwardA compound of formula C11H16N2 gives the IR, 1H NMR, and 13C NMR spectra shown. The proton NMR peak at δ 2 disappears on shaking with D2 Propose a structure for this compound, and show how your structure accounts for the observed absorptions.arrow_forwardPropose a structure for D (molecular formula C9H9ClO2) consistent with the given spectroscopic data. 13C NMR signals at 30, 36, 128, 130, 133, 139, and 179 ppmarrow_forward
- On the basis of the molecular formula, 1H NMR data, and IR data provided, propose a consistent structure. Moleculal Formula: C2H3Cl31H NMR data: δ 3.95 (d, 2H), 5.77 (t, 1H)IR data: 2950 cm–1, and several peaks below 820 cm–1.arrow_forwardAddition of mesitylene to the strongly acidic solvent HF / SbF5 at -45 °C gives a new species which shows a 1H-NMR resonance at δ 4.67 (2H). Draw the structure of this species.arrow_forwardKetones undergo a reduction when treated with sodium borohydride, NaBH4. What is the structure of the compound produced by reaction of 2-butanone with NaBH4 if it has an IR absorption at 3400 cm-1 and M+=74 in the mass spectrum?arrow_forward
- Treatment of 3,4-dibromohexane with strong base leads to loss of 2 equivalents of HBr and formation of a product with formula C6H10. Three products are possible. Name each of the three, and tell how you would use 1H and 13CNMR spectroscopy to help identify them. How would you use UV spectroscopy?arrow_forwardPropose a structural formula for each compound consistent with its 1H-NMR and 13C-NMR spectra. (a) C5H10O2 (b) C7H14O2 (c) C6 H12O2 (d) C7H12O4 (e) C4H7ClO2 (f) C4H6O2arrow_forwardSelect the best answer. Briefly explain the selection. A mechanism is an acceptable explanation.arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning