In the following situations determine the molecular structure of the compound. Show all your work and...
Propose a reasonable structure based on the molecular formula, the 1H NMR, and the proton–decoupled 13C NMR data below. The unknown compound has a molecular formula of C7H16O and * = CH2 by DEPT. Propose a reasonable structure based on the molecular formula, the 'H NMR, and the proton-decoupled 13C NMR data below. The unknown compound has a molecular formula of C7H160 and * = CH2 by DEPT. 'H NMR 3H 8H 13C NMR 2H (CH3)4 Si 26 VIH them...
Propose a reasonable structure based on the molecular formula, the 'H NMR, and the proton-decoupled *C NMR data below. The unknown compound has a molecular formula of C7H160 and * = CH2 by DEPT. 'H NMR 3H 8H HC NMR 2H (CH3), Si 3.5 0.0 40 3.0 2.5 2.0 1.5 1.0 0.5 300-MHZ 'H NMR spectrum ppm (8) "C NMR spectrum ppm (5)
3) For the following questions draw the structure of the compound based off of the molecular formula and NMR that is given. a) CsH10 Draw the structure of the compound. 10 H CH10 PPM b) C3H100 Draw the structure of the compound. ЗН ЗН CgH100 d, 240, 2H 6 PPM c) C6H12O2 (IR stretch: C=0 stretch at 1737 cm) Draw the structure of the compound. 6H tsep, 1H C6H1202
Determine the structure based on the molecular formula and its 1H NMR spectrum (and IR spectrum, if provided). Show the work by providing a table summarizing the data from each spectrum and explain in detail the reasoning. You must analyze each absorption in the NMR and four absorptions in the IR (if applicable). The table for NMR should include: chemical shift (δ value), the splitting, the number of neighbors, the integration, and the assignment of the specific protons responsible for the...
An unknow compound has the molecular formula C5H10O2 has the IR spectrum, and the RMN-^1H show below. a) Propose a structure that is consistent withthe information provided. b) Assign all signals in the spectrum of RMN-^1H. c) Assign at least two bands of the IR spectrum. Note : Remember determine the degrees of unsaturation of the compound. Yave Number, cm 4000 2000 2500 2000 1500 1200 1200 1100 1000 LLLLLLLLLL 100 Absorbance Wavelength, microns
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...
Draw the structure of a compound consistent with the following spectral data. In addition, the IR spectrum of Ah strong band at 1720 cm-1, while the cyclic compound B sho carbonyl peak on its IR spectrum. (10) CH00, (A) C,H O (B) mical shift (δ)Relative area!Chemical shift (6) No. of H зн 2H 2H 2H IH 2.09 3.24 5.06 1.71 2.24 2.49 3.12 5.44 0.5 PPM H-NMR spectrum of A Draw the structure of a compound consistent with the following...
A compound with a molecular formula C5H10O has the following 1H NMR spectrum. Provide a structure that is consistent with this spectrum. 3. A compound with a molecular formula CsHioO has the following 'H NMR spectrum. pound with a molecular formula CsHioO has the following H NMR Propose a structure for this compound. PPM
4. Propose a structure for each molecular formula using the provided H NMR spectrum. (a) CH30 6H IH 1H PPM (b) C6H120 ЗН PPM (c) CaHgBr 2H PPM (d) C&H N 2H 2H PPM
For the following questions draw the structure of the compound based off of the molecular formula and NMR that is given. 3) For the following questions draw the structure of the compound based off of the molecular formula and NMR that is given. a) CsHjo Draw the structure of the compound 10 H CHIO PPM b) CxH100 Draw the structure of the compound. CH400 0,2H ,2H PPM c) C6H1202 (IR stretch: C=0 stretch at 1737 cm') Draw the structure of...