8. The 'H NMR spectrum below corresponds to a compound with molecular formula CH1202 Determine the...
Give the structure that corresponds to the following molecular formula and 1H NMR spectrum: C7H12Cl2 : δ 1.07 (9H, singlet): δ 1.83 (2H, doublet); δ 5.77 (1H, triplet).Draw the structure of the compound that is consistent with the 1H NMR data below. Do not draw any hydrogens in your solution. It must be drawn as a true skeletal structure.
3. Given the 'H NMR spectrum below and a molecular formula of C.HO. provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. IR: 3300 cm' (broad) (5 pts.) 3H, d 3H, 2H, t 2H, 2H, m 1H, bs 1H, m PPM
3. Given the 'H NMR spectrum below and a molecular formula of CaH.O, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. IR: 3300 cm (broad) (5 pts.) зн, d Зн, t 2H,t 2H, q 2H, m 1H, bs 1H, m 4 3 2 PPM 4. In the space below, draw a 'H NMR spectrum for each of the following molecules. Note that only one of these will be graded...
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...
The following is the predicted 1H-NMR spectrum for an unknown compound with molecular formula C6H14O. This compound is a liquid at room temperature, is slightly soluble in water, and reacts with sodium metal with the evolution of a gas. 9H 1 1H 2 1H 31H 4 2H Not Submitted PPM Choose from the constitutional isomers below to assign a structure to this spectrum. CH3 CH3 ba CH2CH3 CH3CH2CH2CHCH2OH a b c d e g CH3CH2CHCHCH3 а ь | OH f...
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...
2. Given the 'H NMR spectrum below and a molecular formula of CsHioO, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. IR: 1710 cm'(5 pts.) 6Н, d 2H, d 1H, s 1H, m 10 PPM -2
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
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.
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...