The IR and 13C NMR spectra are shown for a molecule with the molecular formula of C5H10O. Draw the structure that best fits this data. 80 PPM 4000 3000 2000 + 1500 Wavenumber (cm³¹) my 1000 500 @ Q
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The IR and 13C NMR spectra are shown for a molecule with the molecular formula of C5H10O. Draw the structure that best fits this data.
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- When measured on a spectrometer operating at 200 MHz, chloroform (CHCl3) shows a single sharp absorption at 7.3 δ. (a) How many parts per million downfield from TMS does chloroform absorb? (b) How many hertz downfield from TMS would chloroform absorb if the measurement were carried out on a spectrometer operating at 360 MHz? (c) What would be the position of the chloroform absorption in δ units when measured on a 360 MHz spectrometer?The H1H1 NMR spectrum shown corresponds to an unknown compound with the molecular formula C6H10C6H10. There are no strong IR bands between 2100 and 2300 or 3250 and 3350 cm−1. Deduce and draw the structure of the molecule that corresponds to the spectrum.A 13C NMR spectrum is shown for a molecule with the molecular formula of C4H8O2. Draw the structure that best fits this data. 180 160 140 120 100 PPM 80 Drawing 8 8 20 0 Q
- A 13C NMR spectrum is shown for a molecule with the molecular formula of C5H10O2. Draw the structure that best fits this data. 180 160 140 120 100 80 60 40 20 PPMIdentify the compound with molecular formula CSH12O that gives the IR and 'H NMR spectra shown here. 1600 Wavenumber (cm) 4000 3800 3600 3400 3200 3000 2800 2600 2400 2200 2000 1800 1400 1200 1000 80 600 2 8. 6. 8 (ppm) Identify the compound with molecular formula CoH12O that gives this 13C NMR spectra. 200 180 160 140 120 100 80 60 40 20 8 (ppm)A 13C NMR spectrum is shown for a molecule with the molecular formula of CsH1002. Draw the structure that best fits this data. 180 160 140 120 100 PPM 80 60 40 20 O Q
- 1H 15 2H 3H 2 2H 2H 3H ppmConsider a molecule with the molecular formula of C3H7NO2. The IR and ¹H NMR spectra are shown below. Draw the structure that best fits this data. 4000 3000 2H 2000 1500 Wavenumbers (cm-¹) + 2H 1000 3H 500 ppmA'H NMR spectrum is shown for a molecule with the molecular formula of CeH9Br. Draw the structure that best fits this data.
- Compound CsH12 gives the following H-NMR. Draw the structure of the compound. Draw a box around the structure you want graded. 5.00 1.00 6.04 70 6.5 6.0 4.0 3.5 3.0 25 20 1.5 A student was adding bromine across the double bond of 2-butene to make 2,3-dibromobutane. After taking the NMR, the student discovered they didn't get the product expected. Based on the NMR, what product did they obtain? Draw a box around your answer. 1.00 2.01 |2.00 3.00500 20 8.0 Interpret the 'H-NMR spectrum and assign the correct structure. Please be sure to explain your work. C₂H₁, CL 3.0 7.0 400 4.0 6.0 5.0 -B00 5.0 6.0 4.0 200 7.0 E 3.0 8.0 MA 20 100 9.0 1.0 10.0 (ppm) 가 O Hz 08 (ppm)A ¹H NMR spectrum is shown for a molecule with the molecular formula of C10H12O4. Draw the structure that best fits this data. 1H 11 10 2H 2H U 7 1H 1H ΤΗ 1Η ppm Q