1. How many signals do you expect to see in the 'H NMR of the following...
7. Which compound below best fits the following spectral data? 8. How many signals would you expect to see in the broadband decoupled C^13 spectra of the following compounds? 9. If a proton gave an NMR signal at 3.2 ppm on a MHz NMR, what would the chemical shift be of this proton (in ppm) if the sample was run in 400 MHz NMR? 7. Which compound below best fits the following spectral data? (6 points) H-1 NMR 0.9 ppm...
PART 1 - For the following compounds A. Predict how many signals would be detected in the expected 'H NMR spectrum. B. Label proton groups and determine their multiplicity. c. Predict the chemical shifts of each signal in the expected 'H NMR spectrum of the following compounds from the correlation chart in the last page. <Example> Number of signals O Proton groups Multiplicity Triplet B Multiplet (sextet) c Triplet D Singlet Chemical Shirt (ppm) 0.8-1.0 1.2 - 1.5 3.2 4.0...
3. How many 'H NMR signals would appear in the 1H NMR spectrum of each compounds? CHE CH2CH3 CH3 CH3 cs I CH₂ I type of its CH3 IMMR signed Match each of the following 1 H NMR absorptions to the compounds below, each of which has a one- signal spectrum: 6 0.04, 0.90, 1.42, 2.25, 7.3ppm CH3 нес (H3C),Si— Si(CH3)2 H3C1 CHE C(CH3) CHE
50. For the following compound how many different signals would you see in the proton NMR? (Assume that you can see them all.) A) 4 B) 5 C) 6 D) 7 E) 8 . An organic compound absorbs strongly in the IR at 1687 em. Its 'H NMR spectrum consists of two signals, a singlet at 2.1 ppm and a multiplet centered at 7.1 ppm. Its mass spectrum shows significant peaks at m/z 120, m/z 105 and m/z 77. This...
7. Which compound below be H-1 NMR 0.9 ppm (quartet fits the following spectral data? (6 points) 1.2 ppm (sextet 2 hydrogens), 2.1 ppm (triplet, hydrogens), 4.3 ppm (singlet 3 hydrogens) C-13 NMR 5 signals 25 ppr ppm (CH2); 61 ppm: (CH3) 198 Ppm (C). IR strong peak 1735 cm Ignals 25 ppm (CH): 35 ppm (CH2), 46 ppm (CH2); 61 ppm: em Mass Spee parent M+ = 102 Mass Spec paren ou 0 H2 CH3 HjC Holo H3C- CC...
1. Signal Assignment. Below are a set of ranges where a specific H' NMR signal might be found. 0.5-2.0ppm 2.0-3.0ppm 3.0-5.Oppm 0.5-6.Oppm 5.0-7.0ppm 7.0-8.Oppm 9.0-10.0ppm 10.0-12.0ppm Assign to the slots above where the following highlighted protons might be found. a) CH3-CH2- b) CH-CH2-CH2- c) HC-0 d) H-C(O)-R e) H-O-R ) H-O-C(O)-R g) H;C-Ar h ) H-C-C- j) CH3-CEC ...some groups appear in the same ppm range. [2pts each group correctly assigned) 2. Signal Splitting. Decide what splitting pattern (singlet, doublet,...
5. How many 13C NMR signals (peaks) does each compound exhibit? ed 6. The 13C NMR spectra for the following compounds are shown below. Please assign each signal to its corresponding carbon (label them a-h). 40 20 20 PPM 50 PPM
How many sets of signals would you expect to see in the 1H NMR spectrum of each of the following compounds and label them as Ha, Hb and Hs, etc.? ethyl propyl ketone Diethyl ketone VS cyclopenta-1,3-diene cyclopentene VS 이이 세이어 toluene 1,4 dimethyl benzene VS
PART 2 Draw the most accurate 'H-NMR spectrum you can for the following molecules. Show all signals including an accurate representation of splitting, intensity and position. Assume no signal overlap (i.e. if you expect signals have similar chemical shifts, just place them next to each other). Clearly label the integration value for each signal. Indicate the correlation between each proton (HA, HB, etc) and each signal (label signals A, B, etc.) ppm 12.5 10 11 O ppm 12.5 10 ii...
answer them all thanks Which of the following compounds fits the proton NMR shown below? ЗН 1.0 ppm A) CH,CH,CH_COCH B) CHỊCH COCHẠCH ) CH3COCH_CH.CH D) CH,CCH_CHOCH MacBook Air esc Identify the CAHgCl isomer given the following proton NMR data: doublet 8 1.04 (6H) multiplet 81.95 (1H) doublet o3.35 (21) A) (CH3),CCI B) CHCHCH-CH-CI C) CH3CHCHCH, D) (CH3),CHCH_CI Ос ОА Ma hybridized CH absorption in its mollion tion in c 72 and n o R etina 1725 m. Assume each...