The ^1H NMR spectrum below corresponds to an unknown compound with the molecular formula C_6H_10. There...
The^1H NMR spectrum below corresponds to an unknown compound with the molecular formula C_7H_12. There are IR bands at around 2120 and 3330 cm^-1. Deduce and draw the structure of the molecule that corresponds to the data.
The^1H NMR spectrum below corresponds to an unknown compound with the molecular formula C_4H_8O. Deduce and draw the structure of the molecule that corresponds to the data below.
^1H NMR spectrum below corresponds to an unknown compound with the molecular formula C_4H_8O. Deduce and draw the structure of the molecule that corresponds to the data below.
The^1H NMR spectrum below corresponds to an unknown compound with the molecular formula C_3H_4CI_2. Deduce and draw the structure of the molecule that corresponds to the data below.
The 1H NMR spectrum below corresponds to an unknown compound with the molecular formula C4H7Cl. Deduce and draw the structure of the molecule from the data below. Clearly show stereochemistry where applicable. 3 H H NMR 2 H 1 H (CH3)4Si 1 H 5.0 4.5 4.0 3.5 3.0 2.5 2.0 1.5 1.0 0.5 0.0 300-MHz H NMR spectrun ppm (o)
Please answer the question above. The 1H NMR spectrum below corresponds to a molecule with the formula C4H5O. Its IR spectrum has important bands at 945, 1015, 1665, 3095, and 3360 cm^-1 Deduce and draw the structure of the unknown compound.
Could someone help me with this question? The^1H NMR spectrum below corresponds to an unknown compound with the molecular formula C_5H_8O_2. Deduce and draw the structure of the molecule from the data below.
Need help with number 1. Thanks. An unknown compound has the molecular formula C_5H_10O_2. Its^1H NMR spectrum is shown below (integral values are shown below each peak). Its IR spectrum shows a strong peak at 1740 cm^-1. Determine its structure and assign all peaks on the NMR spectrum.^1H NMR (300 MHz, in CDCl_3) An unknown compound has the molecular formula C_9H_10O. Its^1H NMR is shown below (integral values are shown next to each peak). Its IR spectrum shows a strong...
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.
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...