By citing specific data show that you could distinguish between the two members of each pir of compounds by 1H NMR spectroscopy.
1. a) butyl 2-phenylbenzoate b) benzyl pentaoate
2) a) benzyk 3Z-pentenoate b) benyl 3E-pentaoate
3) a) priopiophenone b) phenyl propionate
By citing specific data show that you could distinguish between the two members of each pir...
How to distinguish between the two members of each pair of compounds by proton NMR spectroscopy? 3. (12 points) By citing specific data, show that you could (or could not members of each pair of compounds by 'H-NMR Spectroscopy. If y significant distinguishing features, mention all of them. Give all refer question. Tato show that you could (or could not) distinguish between the two hy TH-NMR Spectroscopy. If you are aware of several bention all of them. Give all references...
How to distinguish between the two members of each pair of compounds by C-NMR? 4. (12 points) By citing specific data, show that you could (or could not) distinguish between the members of each pair of compounds by 13C-NMR Spectroscopy. If you are aware of several significant distinguishing features, mention all of them. Give all references used to answer the question. a) 1-phenyl-2-pentanone 1-phenyl-1-pentanone OOH OOH 3-bromobenzoic acid b) 3-iodobenzoic acid Electron dona ter resonance effect of iodine, shifch doorsteld
How to distinguish between each pair of compounds by IR spectroscopy? Pretsch pg. 13, IR_3230-2.pptx slides 16-17 (18 points) By citing speciipounds by IR spectrosciu Peferences use 1. (18 points) By citing specific data, show that you could (or could not) distinguish between the two members of each pair of compounds by IR spectroscopy. If you are aware of several significant distinguishing features, mention all of them. Give all references used to answer the question. bony' for the a) meta-ethylbenzaldehyde...
ng Pattern 3. Explain how 'H-NMR spectroscopy could be used to distinguish between the two compounds shown below. Be as specific as possible. [10 Points] CH2COCH3 CH2CH3 4. Predict the approximate chemical shift position for each of the different hydrogens in the 'H-NMR spectrum of this compound. [10 Points] Cl CH2CH2-COCH2CH3 . Predict the multiplicity of each of the signals in the H-NMR spectrum of the
ii) (4 marks) Briefly explain how 1H-NMR spectroscopy would allow you to distinguish between the 3 isomers of butyl alcohol. MOH LOH
(a) Explain how you would distinguish the three isomers below using NMR spectroscopy. Give specific examples of peaks, chemical shifts and splitting patterns that would illustrate the differences (b) Determine the structure of C8H14O from the NMR data below. (c) Draw the 1H-NMR spectrum you would expect for the following compounds. Show clearly the splitting pattern and the integration values.
How would you use IR and 1H-NMR spectroscopy to distinguish between these two isomeric compounds? For IR, consider the absorption of the carbonyl group. For 1H-NMR, consider the number of signals observed. Select the IR frequency and number of NMR signals that is diagnostic for either isomer a or isomer b. Isomer A: N-methylbutanamide Isomer B: N,N-dimethylpropanamide IR: _______ cm-1 a-1680 a-1690 a-1735 a-1810 a-2250 b-1650 b-1690 b-1710 b-2250 1H-NMR: _____ signals a-4 a-5 b-3 b-4 b-5 b-6
Question 6 (2 points) Saved Explain briefly how you could use 1H NMR spectra to distinguish between these three compounds A, B and C. Please provide two different arguments. NO2 NO2 NO2 NO2 NO2 NO2 A B с
please answer #5 5. Which type of spectroscopy (IR, 'H NMR, and/or "C NMR) would be good to distinguish between propanal and propanoic acid? State what you would observe for each compound in each type of spectroscopy and whether that type of spectroscopy would be a good way to distinguish between the two compounds.
3. Which type of spectroscopy (IR, 'H NMR, and/or C NMR) would be good to distinguish between acetone and 2-propanol? State what you would observe for each compound in each type of spectroscopy and whether that type of spectroscopy would be a good way to distinguish between the two compounds.