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Provide a structure for the following compound: EI mass spectrum: two molecular ions of about...
Propose a structure for the compound that has the following spectra: NMR: ? 1.28 (3H, t, J = 7 Hz); ? 3.91 (2H, q, J = 7 Hz); ? 5.0 (1H, d, J = 4 Hz); ? 6.49 (1H, d, J = 4 Hz) ppm IR: 3100, 1644 (strong), 1104, 1166, 694 cm -1 (strong) no IR absorptions in the range 700-1100 cm -1 or above 3100 cm-1 Mass spectrum: m/z = 152, 150 (equal intensity; double molecular ion)
A compound of unknown structure gave the following spectroscopic data: Mass spectrum: M+ = 88.1 IR: 3600cm-1 1H NMR: 1.4 (2H, quartet, J=7Hz); 1.2 (6H, singlet); 1.0 (1H, singlet); 0.9 (3H, triplet, J=7Hz) 13C NMR: 74, 35, 27, 25 a. assuming that the compound contains C and H but may or may not contain O, give three possible molecular formulas. b. how many protons (H) does the compound contain? c. what functional group(s) does the compound contain? d. how many...
For the following questions draw the structure of the compound based off of the molecular formula and NMR that is given. 3) For the following questions draw the structure of the compound based off of the molecular formula and NMR that is given. a) CsHjo Draw the structure of the compound 10 H CHIO PPM b) CxH100 Draw the structure of the compound. CH400 0,2H ,2H PPM c) C6H1202 (IR stretch: C=0 stretch at 1737 cm') Draw the structure of...
1. Given the 'H NMR spectrum below and a molecular formula of CH20, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. IR: 1600-1650 cm' (multiple peaks) (5 pts.) 3H, S 3H. t 2H, d 2H, d 2H, PPM 2. Given the 'H NMR spectrum below and a molecular formula of CH.0, provide a structure. Note you must assign all of the signals in the spectrum below to receive full...
3. Given the 'H NMR spectrum below and a molecular formula of C.HO. provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. IR: 3300 cm' (broad) (5 pts.) 3H, d 3H, 2H, t 2H, 2H, m 1H, bs 1H, m PPM
Deduce the structure of an unknown compound using the data below: Molecular Formula: C10H12O2 IR: 1690 cm-1, 1612 cm-1 NMR: ? 1.4 (3H, t, J = 8 Hz); ? 2.5 (3H, s); ? 4.1 (2H, q, J = 8 Hz); ? 6.9 (2H, d, J = 9 Hz); ? 7.9 (2H, d, J = 9 Hz) ppm Print Calculator- Periodic Table Question 3 of 25 Map Organic Chemistry Roberts & Company Publishers presented by Sapling Leaming Mare Loudon duce the...
Part A The 1H NMR spectrum of a compound which has the molecular formula c4Hao is shown below. Identify the compound. See pages 22-24 of the Chapter 13 notes. 6.45 ppm dd, J 18, 10 Hz, 1H 4.18 ppm dd, J 18, 2 Hz, 1 3.95 ppm dd, J 10, 2 Hz, 1 3.75 ppm quartet, 2H 1.30 ppm triplet, 3H
I am not understanding this assignment at all. Any assistance is very much appreciated. Mass Spectrum: Molecular Ion m/z value and structure of the Molecular Ion. Base Peak m/z value and structure of that ion One other significant peak m/z value and structure of that ion C13 NMR Spectrum-- Draw Structure of Compound on the C13 NMR spectrum and identify each signal with the appropriate Carbon. Proton NMR Spectrum-- Draw Structure of Compound on the Proton NMR spectrum and identify...
2. Given the 'H NMR spectrum below and a molecular formula of CsH60, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. IR: 1710 cm (5 pts.) 6H, 1H, S 2H, d 1H, m NH PPM CHE 310 Homework 9 Due WED NOV 20 3. Given the 'H NMR spectrum below and a molecular formula of CH..0. provide a structure. Note you must assign all of the signals in the...
Give the structure that corresponds to the following molecular formula and 1H NMR spectrum: C4H10O2: ? 1.36 (3H, d, J = 5.5 Hz); ? 3.32 (6H, s); ? 4.63 (1H, q, J = 5.5 Hz)