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- 6:51 A) I B) II Uber Eats C) III Question 3 of 33 Predict which carbon will have the most upfield signal in the ¹³C NMR spectrum. || OH 35 Min D) IV Tap here or pull up for additional resources IV 5 Br Submit NH₂What is the molecule name and the NMR of the molecule below?Refer to the NMR spectrum below. How many unique H's are there in this compound?
- 13. How many unique NMR signals (disregard splitting) would be predicted in the 13C spectrum of the following compound? Circle the best answer. (2 points) な Br A) 2 B) 3 C) 4 D) 5 E) 6A total of how many signals are expected in the ¹H spectrum of the given compound? CI оMagnetically equivalent protons give a single signal in 1H-NMR. How many signals will be observed in the 1H-NMR spectrum of the compound in the figure? (TO). 4 (B). 6C). 8 (D). 10 CH3
- 6) Complete the spectroscopy data tables for a compound with molecular formula C6H12O. Determine the structure of the compound. Any labile protons, if they exist, will not be present in this particular 1H NMR spectrum.The number of peaks in the ¹H-NMR spectrum of a com-pound depends on the number of different kinds (environments)of H atoms. How many peaks appear in the spectrum of each iso-mer of C₄H₁₀and of C₅H₁₂A total of how many signals are expected in the H spectrum of the given compound?
- The H NMR spectrum of which of the compounds below, all of formula C7H1202, would consist of a singlet, a doublet and a triplet only? Circle the structure and label the protons on that structure as (s), (d), and (t), respectively. exo I II II IVHow many unique 1°C NMR signals exist in the spectrum for the compound? HO HO, The number of signals is:how do you figure out what to expect an NMR to show about these two molecules?
