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A: The structure of the unknown compound of molecular formula C8H8O3 is shown below:
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A: The detailed explanation given below:
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Q: 08) An organic compound has the molecular formula C5H12O. The 1H NMR spectrum is shown in the image…
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A: Solution: The step-by-step solution of the given questiona are shown below ---
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Q: Analyze the 13C-NMR spectrum of C8H9NO given below and draw the structure of the compound.
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Suggest structures given the 1H NMR spectra and formulas for each of the compounds below.
C9H10O
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- Suggest structures given the 1H NMR spectra and formulas for each of the compound below. C3H7ClThe following 1H NMR spectra are for four compounds, each with molecular formula of C6H12O2. Identify the compoundsDraw the structure of a compound with the formula C5H10O2 (along with the reasons of choosing it) which, upon analysis, gave key peaks in an infrared spectrum at 3450 cm-1 and 1713 cm-1, as well as the following 1H-NMR spectrum.
- Propose structures for the compound C5H10O whose 1H NMR spectra is attachedUse the 1H-NMRs to determine the structure for the compound with formula: C4H10OThe treatment of (CH3)2C=CHCH2Br with H2O forms B (molecular formulaC5H10O) as one of the products. Determine the structure of B from its 1H NMR and IR spectra.
- Calculate the IHD of C7H6XNO and explain (elucidate) the structure using the 1H and 13C NMR data.Analyze the 1H AND 13C NMR spectrum of C8H9NO given below and draw the structure of the compound.The IR spectrum, 1H NMR spectrum, and 13C NMR spectrum for the unknown compound with the formula C5H12O are given below. Make a structure for the unknown and assign the peaks in the spectra by the provided tables.
- Propose a structure given the 1H and 13C NMR spectra of the unknown compound. Assign chemical shifts to corresponding hydrogen and carbon atoms Molecular Formula: C5H10O3The following are all 1H-NMR spectra for compounds D, E, and F with C6H12 molecular formulas. BR2 is easily bleached in the solution. Suggest a structural equation for Compounds D, E, and F and explain the cracking form of the signal.Determine the following for the compound C6H15N a.) degrees of unsaturation b.) Assign the principal IR absorption bands above 1500 c.) draw the structure of the compound d.) label the protons on your structure with letters and assign them to peaks on the NMR spectrum.