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- How many signals would be in a CNMR AND HNMR for this product? Please explain in depth.Why is this the correct spectra for these molecules? Identify specific absorption band which identifies each characteristic functional group of the molecule chosen.Determine the structure for the molecule that most likely produced these spectra. Use all pictures
- how many peaks wouldyou expect to see in the 13CNMR spectrum of this substance ?Compound C6H10O has the infrared spectrum shown below. Draw areasonable structure that is consistent with this data. Please explain work. Calculate the Rvalue first! -This compound has two common functional groups.use the following spectra to fill out table. what is unusual about the wavenumber of the C=O? explain. thank you
- Explain why TMS has a lower chemical shift than its carbon analog, dimethylpropane, (CH3)4C.In very high resolution spectra of HCl, each one of the narrow lines observed is split into two lines: one about one third the height of the neighbor (you may be able to just see this effect in your data). Suggest a possible origin for the splitting of these lines.Each peak in the spectrum below can be used to provide a measure of the mass of this protein, you can work out the charge associated with each peak, and measures can be averaged to find the overall mass. Use simultaneous equations to find the charge associated with each peak in the spectra below, which will allow you to calculate the average mass of each species. Include an estimate of the error associated with this measure
- Refer to the given HNMR spectra, and determine the structure of the molecule. Corroborate your answer with the FTIR spectrum. Label which hydrogens refer to which chemical shifts.i want example of HNMR signals that out of expectation because of dimagnetic anisotropy or resonanceDetermine the structure for the molecule that most likely produced these spectra.