What is the molecular formula and structure?
Mass Spect: 74
IR:2880-2969, 3200-3602
Proton NMR: 0.90 (triplet, 3H), 1.20 (doublet, 3H), 1.48 (quintet, 2H), 3.58 (broad singlet, 1H), 4.05 (sextet, 1H)
Carbon NMR: 9.6, 23.4, 32.8, 70.4
The IR stretching around 3200-3600 is broad and suggest an -OH group.
From the splitting rule of (n+1) where n is number of adjacent protons can be very well employed to Know the number of hydrogens on each carbon. That is a quintet means 4 adjacent protons.
13C suggests 4 different types of carbon.
What is the molecular formula and structure? Mass Spect: 74 IR:2880-2969, 3200-3602 Proton NMR: 0.90 (triplet,...
Using the NMR, IR, and MS figure out what the compoud is. ** identify the molecular structure througu NMR, IR and MS CHEM 100L Lab 3 NMR Problems Unknown 1 CH 0 M-a 102 Relative Intensity 20 30 40 50 70 80 60 m/z water, not part of sample 1-2975-2877 9H, singlet 2H, 3H, quartet triplet ppm Unknown 2 C,H,O tensity 119 Relative 3200-2600 1680V 3H, singlet 2x 2H, doublet 1H, singlet ppm Unknown 3 C,HO, Relative Intensity 3090 3035...
Propose structures that fit the following formula and NMR data. (a) C3H100 singlet at 2.10 8 (3H) doublet at 0.958 (6H) multiplet at 2.43 8 (1H) (b) C10H14 singlet at 1.30 8 (9 H) singlet (broad) at 7.308 (5H) (c) C9H11Br quintet at 2.15 8 (2H) triplet at 2.758 (2H) triplet at 3.38 8 (2H) singlet at 7.22 8 (51) IR spectrum: strong peak near 1720 cm (d) C18H14 O2 Singlet at 2.20 8 (3H) Singlet at 5.08 8 (1H)...
Identify what structure these are based on the NMR and DRAW the structure. 4) Chemical Formula: Cl,BrO:S IR: strong broad peak at 3300cm1, strong peak 1720 cm1 Singlet, 3H Quartet, 2H Singlet, 1H Triplet, 2H Triplet, 1H 12 10 PPM
Draw the structure that gives the NMR below. The compound has the molecular formula, CsH1002. Signal at 4.38 (broad singlet, 1H), 3.49 (triplet, 2H), 2.40 (triplet, 2H), 2.10 (singlet, 3H), and 1.86 (pentet, 2H). IR shows a broad band at 3350 cm and a strong band at 1710 cm (in addition to others). Make sure to indicate (label) which hydrogen gives which signal. PPM
Draw the structure of the compound whose molecular formula is C9H10O and has the following proton NMR data: triplet at 1.2 ppm, integrates to 3H quartet at 2.7 ppm, integrates to 2H doublet at 7.3 ppm, integrates to 2H doublet at 7.7 ppm, integrates to 2H singlet at 9.9 ppm, integrates to 1H What are the reagents needed for each of the following transformations? CH3CH2OH a., CH3CH2Br 6 ChọCH2CHCH3 CH3CH2CCH3 CH3CH2CCH3
Draw the structure of the compound whose molecular formula is C9H10O and has the following proton NMR data: Draw the structure of the compound whose molecular formula is C9H100 and has the following proton NMR data: triplet at 1.2 ppm, integrates to 3H quartet at 2.7 ppm, integrates to 2H doublet at 7.3 ppm, integrates to 2H doublet at 7.7 ppm, integrates to 2H singlet at 9.9 ppm, integrates to 1H Take a photo of your answer and upload it...
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...
What is the structure of this compound? 1. Molecular Formula: CHCI 'H NMR 6 3.42 ppm, 1H, pentet 61.80 ppm, 2H, quartet 6 1.73 ppm, 2H, doublet 6 1.56 ppm, 2H, triplet 6 1.53 ppm, 2H, pentet 60.99 ppm, 6H, singlet PC NMR 8 57.2 ppm, 10 6 49.3 ppm, 1C 6 38.4 ppm, 1C 6 37.7 ppm, 1C 6 33.3 ppm, 10 6 30.9 ppm, 2C 8 22.4 ppm, 1C 60 50 40 10 IR: 2964 cm(s) 713 cm...