Need it ASAP please!!! Which compound from the list (MW 130) matches the mass spectrum? 45...
Please help with identifying this compound? Need to draw the
structure
14.01 Mass Spectrum 13C-NMR Spectrum CHO M**= 60 Relative Intensity 10 15 20 25 30 40 45 50 35 m/z 55 60 200 180 160 140 120 80 60 40 20 100 ppm IR Spectrum 1H-NMR Spectrum o Chem. shift Ret area Porto age are 3.5822.00 226 157 094 Singlet (hare some into the rest 1.00 2.00 3.00 1466 3333 2963 11 10 Ppm
need help with both questions please!
3. The 'H and 1C NMR spectra of a compound are given. The mass spectrum shows a M' with m/=154. The elemental analysis is %C, 70.11; %H, 7.19 ; %F. 12.32. Determine the structure of this compound. (5 pts ca Hi O F 3H nso 3H 41H t00 PPM 130 140 PРM 4. The 'H and "C NMR spectra of an unknown compound are shown below. The compound's mass spectrum shows a molecular ion...
Explain why the
IR corresponds to a particular compound of those that are possible
based on BP and why it couldn't be any of the others -mention at
least 3 IR peaks that are present that correspond to functional
groups in your molecule, and discuss specific peaks that were
either present or absent that allowed you to rule out the other
compounds possible based on the boiling point. Reference your IR
spectra as figures.
the boiling
point for unkown 2:...
Identify the compound from the following mass spectrum and
information. Please tell me how you determined what the compound
is.
4. Identify the compound from the following mass spectrum and information 29 100 50 28 90 10 50 60 70 80 100 110 a 30(M) 31 m/z 12 13 14 15 16 28 29 32 Rel 0.07 3.3 4.3 4.4 1.7 31 100 89 1.3 0.21 Abund CO
I need help with scheme 1 please.
Scheme 1: Compound 1 Compound 2 (b) OH (a) + OH Compound 3 Compound 4 Scheme 2: pka increased from 3 (salicylic acid) to 8.5 (Compound 1) H: 607 Laboratory Data: Compound 1: MW: 166.18 C. 65.05 0:28.88 Compound 2: MW: 167.00 C: 28.77 IR: 1739 cm (broad, strong) 'H NMR: H: 423 Br. 47.85 O: 19.15 singlet, 2H quartet, 2H triplet, 3H 2 PPM 13C NMR: 180 160 140 120 100 PPM...
. in the list on unknowns , pick the one that matches your
spectra... based on the information given, what can you say about
the graph
New_Spectrosc.+of+Unknowns Spectroscopy of Unknowns Diphenylmethane Benzaldehyde 2-Bromopropane Propanal Styrene Dilsopropyl Ether Ethoxybenzene Toluene p-Methoxybenzaldehyde 1,1-Diphenylethene 1-Chloro-1-Phenylethane 1-Chloro-2-Phenylethane Benzyl Cyanide Benzyl ethyl ether 1-Bromobutane lodoethane p-Bromoethylbenzene Benzonitrile 1-Bromo Propane Ethyl p-Bromobenzoate Ethyl Benzoate Diethyl Succinate 1,4-Dichlorobutane 1,3-Dichloropropane 1. Phenylethanol 2-Phenylethanol 2-Propanol Chlorodiphenylmethane 2-Bromobutane Ethyl Acetate 1-Phenyl-1-Propanone 2-Methyl-1-Phenyl-1-Propanone Acetophenone 2-Butanone Ethanol List Spectroscopy Compound K list...
please show step by step. Thank you
O. Which CsH120 compound gives the following EI mass spectrum? 00 45 80 60 40 20 M (88) 73 0 10 30 40 50 m/z 60 70 80 90 100 Relative Abundance 20
need help on quetion 6 & 7
6 HAMK 1 CNMR 240 220 200 180 140 160 120 100 60 40 20 ppm IR MS 404 3000 2000 Propose a compound for that would furnish all of the above spectra. (1 pt) go zo arbitrary intensty 7 H NMK 12.0 10.5 9.0 7.5 6.0 4.5 3.0 15 C NMR 240 220 160 200 180 140 120 100 Ppm IR tóo Propose a compound that would furnish all of the above...
Hints for identifying compounds in multiple-choice problems (problems 1:5); 1. Closely compare the given compounds. Determine which piece of information (molecular weight from MS, number of peaks in the NMR, presence of a special functional group in the IR, etc) would be the easiest for distinguishing between the given compounds. You might not need to use all types of given spectra to find your correct compound! 2. Based on your answer from step 1, consult the appropriate spectrum first. For...
need help elucidating this please
IR Spectrum liquid 4000 3000 2000 2000 1600 V (cm) 1000 1200 1200 00 100F Mass Spectrum M . 152 280 80 120 180 200 240 40 m / expansion 13C NMR Spectrum (100 O MHE. COCI, solution 130 120 pm DEPT CH CH. CH 10178 por proton decoupled 08 (ppm) 40 80 120 200 160 'H NMR Spectrum (400 MH. COCI, solution) 70 74 pp 5 4 3 2 8 (ppm) 10 9