4. The H NMR spectrum shown below is for a compound with the formula CgHi9lN a)...
Compound E, chemical formula C5H10O2 , is a volatile liquid (boiling point 88°C). The 13C-NMR spectrum shows signals at ? 171.0, 68.3, 23.0, and 17.6 ppm. The predicted 1H-NMR spectrum is shown, propose a structure for compound E. Compound E, chemical formula C5H1002. is a volatile liquid (boiling point 88°C . The 13C NMR spectrum shows signals at ppm. The predicted 'H-NMR spectrum is shown, propose a structure for compound E. 1710, 68.3, 23.0, and 17.6 3H 6H 1H PPM...
2. Given the 'H NMR spectrum below and a molecular formula of CsH60, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. IR: 1710 cm (5 pts.) 6H, 1H, S 2H, d 1H, m NH PPM CHE 310 Homework 9 Due WED NOV 20 3. Given the 'H NMR spectrum below and a molecular formula of CH..0. provide a structure. Note you must assign all of the signals in the...
3. From the NMR spectrum below, determine the structure of the compound. The molecular formula is C4H7BrO2 . There are no 1H NMR signals outside of the region shown. 3. (5 points) From the NMR spectrum below, determine the structure of the compound. The molecular formula is C4H-BrO2. There are no 'H NMR signals outside of the region shown.
8. The 'H NMR spectrum below corresponds to a compound with molecular formula CH1202 Determine the structure, label the unique sets of hydrogens and then use these labels to mark the corresponding signals. (4 pts.) s, 9H s, 2H bs, 1H 10 6 2 P-03-15 ppm
Shown above is the 1H-NMR spectrum of a compound with the formula C5H10O2 . Choose from the constitutional isomers below to assign a structure to this spectrum. 3H 2H 3H 2H PPM Shown above is the 'H-NMR spectrum of a compound with the formula C5Hi002. Choose from the constitutional isomers below to assign a structure to this spectrum a b C CH3CH2CH2CH2COH CH3CH2COCH2CH3 CH3CH2CH2COCH3 (Choose the letter corresponding to the correct structure from the drop-down list provided.) Correct Structure: Assign...
1. Given the 'H NMR spectrum below and a molecular formula of CH20, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. IR: 1600-1650 cm' (multiple peaks) (5 pts.) 3H, S 3H. t 2H, d 2H, d 2H, PPM 2. Given the 'H NMR spectrum below and a molecular formula of CH.0, provide a structure. Note you must assign all of the signals in the spectrum below to receive full...
2. Given the 'H NMR spectrum below and a molecular formula of C-H100, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. IR: 1710 cm: (5 pts.) 6H, 1H, S 2H, d 1H, m PPM
4) All signals in the 'H NMR below correspond to particular hydrogens in the molecule. Assign the NMR spectrum by labeling each proton in the molecule with the appropriate lettered signal. OMe 3H, S HO 3H, S 4H, m 1H, s 1H, br PPM 6H, d 3H, d 2H, S 3H, m 1H, q1H, sept PPM
2. Given the 'H NMR spectrum below and a molecular formula of CH.0. provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. IR: 1710 cm (5 pts.) 6H, d 2Hd 1H, m PPM
6. The 'H NMR spectrum of a compound with molecular formular CaH10O is shown below. Determine the structure of the compound and assign the 'H NMR signals. 4 2