she major 4. Draw the correct structure for the compound with the nmr shown below which...
choose the correct structure for the compound whose nmr is shown below X3 Q10 G6 Choose the correct structure for the compound whose nmr is shown below. Chemical Formula: CsH N 2H 1Η nonet illu PPM CN CN
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
1)Draw the structure of the compound that matches the following simulated DEPT 13C NMR spectra below. The molecular formula of the compound is C4H8O. 2) For light with a wavelength of 3.00 ?m, calculate the corresponding wavenumber value.... Answer is in cm-1 3) Mass spectral analysis of 1-cyclohexylpropan-2-one results in several fragmentation pathways. Complete the mechanism below and give the major products for the McLafferty rearrangement pathway. Include all nonbonding electrons and charges.
The H-NMR spectrum of an unknown compound (formula CaHgO2) is shown below. Draw the structure of the unknown compound. Question 5 4 1 6 5 8 10 11 Ppm The 13C-NMR spectrum of an unknown compound (formula CgH180) is shown below. Its 1H-NMR spectrum only shows one singlet at 1.2 ppm. Draw the structure of this unknown compound. uestion 2 220 200 160 140 120 PPM 100 80 240 180 60 40 20 Create OscerSketch Answer 2 What would be...
Treating the compound shown below with ethanol will give one major product: CH,CH,он (7 pts) Using the 'H NMR for the product given below, draw the product in the box above a. 6H 3H 3H 2H 1H 1H 1H 1H PPM b. (8 pts) Assign the NMR below for the corresponding chemical shift values (s) singlet, (d) (t) triplet, and (q) quartet: doublet 3.2 (d) 5.7 (d) 5.6 (d) 1.4 (s) 3.9 (q) 1.2 (t) 3.4 (d) 1.0 (s)
Draw the structure that gives the NMR below. The compound has the molecular formula, CsH1002. Signal at 4.38 (broad singlet, 1H), 3.49 (triplet, 2H), 2.40 (triplet, 2H), 2.10 (singlet, 3H), and 1.86 (pentet, 2H). IR shows a broad band at 3350 cm and a strong band at 1710 cm (in addition to others). Make sure to indicate (label) which hydrogen gives which signal. PPM
The 1H-NMR and 13C-NMR spectra of an unknown compound (formula C8H10) are shown below. Draw the structure of the unknown compound. The total integration of the peaks at around 7 ppm is 4. The integration of the peak at around 2 ppm is 6. 7 6 5 4 3 ppm TTTTTTTTTTTTTTTT 200 180 160 140 120 100 80 60 40 20 0 pom CH3 Create OscerSketch Answer 8 Incorrect: Answer has an incorrect structure.
Draw the structure that gives the NMR below. The compound has the molecular formula, CsH1002. Signal at 4.13 (triplet, 2H), 2.04 (singlet, 3H), 1.73 (sextet, 2H) and 1.01 (triplet, 3H). IR shows strong bands at 1710 cm-1 and 1200 cm 1 (in addition to others). Make sure to indicate (label) which hydrogen gives which signal. र PPM
Draw the structure that gives the NMR below. The compound has the molecular formula, C5H1002. Signal at 3.61 (singlet, 3H), 2.32 (triplet, 2H), 1.68 (sextet, 2H) and 0.99 (triplet, 3H). IR shows strong bands at 1710 cm 1 and 1200 cm 2 (in addition to others). Make sure to indicate (label) which hydrogen gives which signal. Enter Full Screen PPM
2X. Draw the structure of the compound having a moleculer fomula SotiN with the proton NMR spectrum shown. 2H trip. doub 1H tip. PPM