Can you please explain how you got your answer? Thank you!
Can you please explain how you got your answer? Thank you! For each of the following...
If you could help explain the chart above, that would be awesome. 4. Analyze the IR spectrum of your product, filling in the table below. You should utilize your course textbook (pp. 764-766), if you need assistance. Please note that the frequency given below should be exact (one number), not a range. Use the frequency of the center of the band at its strongest point. Then, on the spectrum itself, mark the characteristic bands at their strongest point with a...
Answer the following question as "every time, never or occasionally" true. Explain your answer. A) Compounds with alkynes have a signal above 3000 cm-1 B) Compounds consisting alcohol have broad signal representing O-H (stretch), signal above 3000 cm-1 C) Compound with NH2 (bend) signal above 3000 cm-1 D) Compound with alkenes have C=C (stretch) signal between 1600 and 1700 cm-1 E) Ethers do not have a noticeable signal for C-O (stretch)cause the ether functional group is non-polar
Please help me correct the wrong answer. If you could also tell me what I did wrong that would be fantastic, thank you! Lopt.) 10/23/2019 7. (15-ptst Propose structures for the following compounds based on the spectral data provided. Please show or explain all work. All IR absorptions above 1500 cm are given. 7a) Molecular formula CiH4O IR peak at 30o0-2850 cm N SP C 1.10 ppm (doublet, 30 integration units) 3.60 ppm (septet, 5 integration units) 1HNMR data: Aa...
Please help determining this structure and explain how you got to that structure please because I’m lost IR Spectrum 3000 1600 1200 conjug UV Spectrum V (cm') Mass Spectrum λmax 217nm (log10ε 4.1) solvent: mechanol M+ 112 C5H403 口-4-81294" 40 80 120 160200 240 280 13C NMR Spectrum (100.0 MHz, CDCI, soktion) no CHz proton decoupled 200 160 120 80 40 0 δ(pp H NMR Spectrum (400 MHz, CDC, sokudion) Zpea 3h 6.75 6.70 ppm 225 2.20 ppm ET 10...
Please explain clearly how they got the answer, thank you! Please explain clearly how they got the answer, thank you! A proton is accelerated from rest through a potential difference of 2.5 kV and then moves perpendicularly through a uniform 0.60-T magnetic field. What is the radius of the resulting path?
please write clearly so i can read your writing. Thank you! 1. For the following compounds, what fragments would you expect to see on the MS spectrum. Which would be the base peak? CH3 CH;-C-Br CH:CH CH:CH-OCCH.CH.CH CH 2. Rank the following compounds from highest wavenumber to lowest wavenumber for their C= absorption bands: b. 3. Give approximate wavenumbers for the major characteristic IR absorption bands that would be given by each of the following compounds:
which of the following would you expect to have a longer lambda max? explain? pls answer all the questions Which of the following would you expect to have the longer Ama? Explain. 18. How can UV-visible spectroscopy be used to monitor a chemical reaction? 19. Which of the following would show a C-O stretch at the lowest frequency in its IR spectrum? 20. O NH2 ОН OCH3 I1 II IV V Which of the following would be likely to exhibit...
Please explain how you proposed the structure. Thank you! The 'FI-NMR spectrum shown is that of a compound with formula C,H,O,. This compound has an IR absorption at 1716 cm. Propose a structure.
Can you explain these questions with full working out and answers please. Also, what does m/z 72 molecular ion mean in this question? Thank you! Elemental analysis of an unknown compound reveals that it oontains (pnly) the elements C, H& O, and that it contains 66.6 % carbon and 11.2 % hydrogen by mass. The mass spectrum of this compaund contains a molecular ion signal at m/z 72. The IR spectrum of this compound contal ns a strong signal at...
please please please help me. thank you H OCH3 How many different kinds of H signal would you see in the H NMR of the WHOLE molecule? Enter your answer here How many sub-peaks would you expect in the H NMR signal of the indicated H? Enter your answer here Where would you expect the C=O bond to show up in the IR? O 3200-3400 cm-1 (broad) O 3200-3400 cm-1 (doubled) O 3300 cm-1 (sharp) O 3100 cm-1 O 2950...