For each of the following compounds, sketch both a 'H NMR spectrum and a 1°C NMR spectrum. In the 'H NMR spectrum, pay attention to the splitting patterns and include the integral trace. (Ignore long-range coupling.) (a) (b) .CI (c) H3C
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- a) Interpreted the analytical data reported, you should include reference to the IR, and NMR chemical shifts, integration and observed splitting patterns?b) Identify the compound which corresponds to the unknown, and provide a reason?c) Provide reasons why the other 8 structures do not fit with the reportedanalytical data?Part 3B Set 1. Can 1H NMR spectroscopy be used to differentiate between the two compounds? Briefly explain why or why not. Predict the 1H NMR spectrum for each compound (include integration, multiplicity, and approximate chemical shift). Either draw the actual spectrum or put in a data table format.The HNMR , CNMR , 2D NMR SPECTRA OF COMPOUND M1 ARE ATTACHED. WHAT IS STRUCTURE OF IT ? IS IT SYMMETRICAL REGARDS TO ITS CNMR SPECTRUM ? WHAT IS THE STRUCTURE SUGGESTION AND WHY ?
- Please provide a structure consistent with the following IR, 13C NMR, and 1H NMR spectra. Assign at least two bands in the IR and assign all protons in the 1H NMR/13C NMR spectrum. Show calculation of degree of unsaturation and explain your reasoning.Provide a detailed analysis of IR, Mass, 1H NMR and 13C NMR data for the following compound.Provide the structure or SMILES of the compound with molecular formula C8H8O and correlates with the NMR shown in the image
- (a) Compound A has molecular formula C9H18O but shows only one singlet in the 1H-NMR spectrum. Suggest a structure for A and explain your reasoning. (b) Compound B has molecular formula C10H14. The IR, mass, 1H-NMR, and 13C-NMR speca are shown below, they are also downloadable for closer inspection by clicking the link under the spectral data. Suggest a structure for B and explain your reasoning.Shown on the next two pages are the mass, IR and NMR spectra for anunknown organic molecule. Based on the spectra provided, determine thestructure of the molecule. You do not need to assign spectral peaks.Remember to ignore the 13 C NMR triad at 77 ppm that comes from the NMRsolvent.Please give the correct answer to the following NMR spectroscopy question and provide detailed solutions of the answer.
- Analyze the 1H NMR data and talk about the coupling, splitting pattern, equivalents, and the j coupling, and the hydrogensThe molecular weight of the compound is 126. Deduce its structure based on molecular weight. HNMR,IR, and 13C NMR data provided..Give the structure for two isomers of molecular formula C4H10O which are consistent with the ^1H-NMR spectra shown below.