2. Match each 'H NMR spectra with one of the following compounds: CH ભવન, ભo as...
2. Which of the following compounds would be expected to show spin-spin splitting in their 'H NMR spectra? (Check the appropriate Box). No Splitting Splitting Compound cm No Compound Splitting Splitting (CH3)3C-O-CH (CH3)2CH-O-CH3 Br-CH2CH2CH2-Br Br-CH:CH-Br H₂CT , CH₂
13-39 Sketch your predictions of the proton NMR spectra of the following compounds. (a) CH-0-CH.CH ~ NH₂ (b) (CH3),CH-C-CH CH; (1) CH-O CH (c) CI-CH2 - CH2 - CH2-a но NO₂ 0 H₂CCCC_CH₃ H 13-40 NH2 Tell precisely how you would nee the nton NMD
NMR: Interpret the NMR spectra for Thymol Match each homotic H or groups of H to a specific peak and explain the multiplicities in each peak the spectra 'H NMR spectrum 6H Зн 3H ppm
the following 1H NMR spectra are for four compounds each with molecular formula C6H12O2. identify the compounds. 69. The following 'H NMR spectra are for four compounds each with molecular formula C H 202. Identify the compounds. a. 3 10 D 0 n 10 9 00 8 (ppm) frequency b. 3 13 0 7 8 6 4 10 8 (ppm) C. 3 0 10 5 4 8 (ppm) frequency 3 1 0 9 8 7 5 10 6 8 (ppm)
Based on the IR and NMR spectra, determine the structure of each of the following compounds A) The compound with the formula CHN Based on the IR and NMR spectra, determine the structure of each of the following compounds A) The compound with the formula CHN LLLLLLL B) The compound with the formula C,H03 11 10 We were unable to transcribe this imageD) The compound with the formula C, H, NO4 Te 200 180 160 E) The compound with the...
Identify the compounds, please and thank you!!! The 'H NMR spectra for two esters with molecular formula C8H2O2 are shown next. Part A Draw the structure of ester with the following H NMR spectra: 10 9 8 (ppm) frequency 0 . . ®. H1200 mA CO+ \'Z Ĉ AOOOOOO Submit Previous Answers Request Answer X Incorrect; Try Again; One attempt remaining Part B Draw the structure of ester with the following H NMR spectra: 9 8 7 6 2 1...
mass spectrometry matching to graphs 1. (2 points) Match the following mass spectra below to the correct structure below. One structure per spectra. All four compounds will not be used. A) CH:CH-CH(CH3)2 B) CH:CHOHCH.CH C) CH.CH:OCHCH D) CH:CH NHCH.CH Relative Intensity 10 20 30 40 50 60 80 90 100 110 120 70 /z m Relative intensity
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
To give you more practice with analyzing NMR spectra, match each of the following 'H-NMR spectra to one of the five possible compounds (structures below). Assign the NMR peaks to their respective hydrogens. Possible compounds: CH2. (H3 diethyl malonate p-ethylanisole OH 3-methylbutanal 1-pentene 1-propanol 6.0 2.0 4.8 4.6 4.4 4.2 4.0 3.8 3.6 3.4 3.2 3.0 2.8 2.6 2.4 2.2 2.0 1.8 1.6 1.4 1.2 1.0 ppm a. 1.80 1.70 1.60 1.50 1.40 1.30 3.0 ( 2.0 | 2.0 2.32...
NMR spectra for each of the compounds with a chemical shift, multiplicity and H. O.