need help on both question IHNMR cNmR * ms Which of the compounds below gives the...
HNMR --CNMR arbitrary intensity 200 100 100 100 120100 2 020 20 ppm MS Which compound below gives the spectra above? (1 pt)
need help on quetion 6 & 7 6 HAMK 1 CNMR 240 220 200 180 140 160 120 100 60 40 20 ppm IR MS 404 3000 2000 Propose a compound for that would furnish all of the above spectra. (1 pt) go zo arbitrary intensty 7 H NMK 12.0 10.5 9.0 7.5 6.0 4.5 3.0 15 C NMR 240 220 160 200 180 140 120 100 Ppm IR tóo Propose a compound that would furnish all of the above...
2. This question continues on the next two pages. The compounds that gave each ot the ollowing IR an alkene. Some of the compounds may contain more than one type of car (1 pt per spectrum 4 pts) spectra contain a carbonyl. Some of them also contain an aromatic ring and/or bonyl or CE low each spectrum indicate whether the compound contains an aldehyde, 1o amide, 20 amide, carboxylic acid, ester, ketone, or strained cyclic ketone. Below each spectrum indicate...
QUESTION 18: Which of the following compounds gives a 1M aqueous solution having the highest pH? A. (CH3)4N+OH– B. (CH3)4N+Cl– C. (CH3)3N D. (CH3)3NH+Cl– QUESTION 19: The overall conversion RBr →→ RCH2NH2 can be accomplished by successive application of which of these sets of reagents? A. Mg, ether; then NH3 B. NaN3; then LiAlH4 C. NaCN; then LiAlH4 D. H2C=O; then NH3 E. H2NOH; then LiAlH4 QUESTION 20: Which sequence is suitable for preparing butylamine from 1-propanol? A. KMnO4, then...
i need help on both questions... 12. Which one of the following compounds is more likely to have its OH bond broken? Why? OH Н.С. a. CHE H O HC-C H OH b. 13. Which one of the following compounds reacts with C2H5OH to produce the ester CH.COOC2Hs? Write the balanced equations, showing the reactants and the products. CH3CHO CH3COCH CH3COOH CHOCH.
need help 4. Assume that you have samples of the following two molecules, both with the formula CsH160. a) Suppose you are given one of the above molecules (but not both). How could you use an oxidation reaction to determine which molecule you have? Briefly explain with text and reasonable sketches. b) Suppose you are given one of the above molecules (but not both). How could you use dehydration reaction to determine which molecule you have? Briefly explain with text...
Hints for identifying compounds in multiple-choice problems (problems 1:5); 1. Closely compare the given compounds. Determine which piece of information (molecular weight from MS, number of peaks in the NMR, presence of a special functional group in the IR, etc) would be the easiest for distinguishing between the given compounds. You might not need to use all types of given spectra to find your correct compound! 2. Based on your answer from step 1, consult the appropriate spectrum first. For...
of the four compounds listed below which would produce the spectra below? Which molecule is consistent with both of these IR and TH NMR spectra? 100 6H 50 3H 1H 4000 3000 1000 500 2000 1500 WAVENUMBERS Na PPM onthlon OB. Ос. OD OH
Use the IR and MS data to elucidate the structures of the compounds below. Identify the M and other necessary peaks in the mass spectra below. Give the functional group responsible for the IR signals. IR: (1 709) sharp, strong (1607-1653) weak MS: ID 4 peaks 100- Relative Intensity orta pripreme 10 20 30 40 50 60 70 80 90 100 m/z 110 120 IR: (1753) strong (1602 - 1658) weak MS: ID 4 peaks 100 MS-NU-18 Relative Intensity 10...
I need help with this Unknown! Worksheet 4: Identification of Unknown Organic Compounds Reading: For a quick video about the "Rule of 13" https://www.youtube.com/watch?v=2YNE7w_GQlo Introduction One of the most important tasks that chemists are faced with is the separation and identification of compounds from mixtures. Gratifyingly, chemists have multiple tools in the quest to identify unknown organic compounds. Infrared spectroscopy is useful for determining functional groups that may exist in a molecule. NMR spectroscopy tells information about the connectivity of...