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.
Skeletal structure of the first compound:
Explanation:
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Skeletal structure of the 2nd compound:
Explanation:
Give the structure that corresponds to the following molecular formula and 1H NMR spectrum
Give the structure that corresponds to the following molecular formula and 1H NMR spectrum: C7H12Cl2: ? 1.07 (integral = 6203, s); ? 2.28 (integral = 1402, d, J = 6 Hz); ? 5.77 (integral = 700, t, J = 6 Hz). Note: The integrals are given in arbitrary units.
Give the structure that corresponds to the following molecular formula and 1H NMR spectrum: C7H12Cl2: δ 1.07 (integral = 6203, s); δ 2.28 (integral = 1402, d, J = 6 Hz); δ 5.77 (integral = 700, t, J = 6 Hz). Note: The integrals are given in arbitrary units.
Give the structure that corresponds to the following molecular formula, reaction data, and 1H NMR spectrum: This compound undergoes catalytic hydrogenation to give 2,2,4-trimethylpentane. Give the structure that corresponds to the following molecular formula, reaction data, and ^1H NMR spectrum: This compound undergoes catalytic hydrogenation to give 2,2,4-trimethylpentane.The magenta numbers in the spectrum are the relative integrals in arbitrary units, and the violet numbers are coupling constants.Give the structure that corresponds to the following molecular formula, reaction data, and 1H...
Give the structure that corresponds to the following molecular formula and 1H NMR spectrum: C4H10O2: δ 1.36 (3H, d, J = 5.5 Hz); δ 3.32 (6H, s); δ 4.63 (1H, q, J = 5.5 Hz)
Give the structure that corresponds to the following molecular formula and 1H NMR spectrum:
The following spectroscopic data corresponds to an an unknown compound with the molecular formula C4H8O2. Deduce and draw the structure of the compound that corresponds to the data 1H NMR: δ 4.07 (quartet, 2H), 1.97 (singlet, 3H), 1.18 (triplet, 3H) ppm. "C NMR: δ 170, 60, 20, 14 ppm.
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
Give the structure that corresponds to the following molecular formula and 1H NMR spectrum: C2H2F3I: ? 3.56 (q, J = 10 Hz)
Give the structure that corresponds to the following molecular formula and 1H NMR spectrum: C4H10O2: δ 1.36 (3H, d, J = 5.5 Hz); δ 3.32 (6H, s); δ 4.63 (1H, q, J = 5.5 Hz) can you explain how to get the answer how do you use the shift, d,s,q to figure out the problem and the importance of J
Give the structure that corresponds to the following molecular formula and 1H NMR spectrum: C5H10: ? 1.5, s