Identify each carbon and H HNMR and CNMR bands with letters to the corresponding part on...
Identify each carbon and H HNMR and CNMR bands with letters to the
corresponding part on the structure provided.
IH, singlete multi, I H multi, 2 H multi, 2 H 10 0 PPM 2 señales 140 100 PPM 120 40 20 200 180 160 80 0 60 140
Identify each carbon and H HNMR and CNMR bands with letters to the
corresponding part on the structure provided.
Los H del CH2 son adyacentes a un centro quiral, por lo que cada H es distinto. dd = doblete de doblete m. 10 H ΠΗ dd, IH 2H dd, IH dd, IH PPM 7 señales 140 120 100 PPM 60 40 20
Determine structure of unknown compound by deducing the formula
and analyzing the spectra.
Part C:S IR/HNMR/CNMR Unknown #93 MW=134 AMU / ring SOC-H dromul 5,311 - Overlapping Signals, 4 1,34 HEP-11-24 ppm 4 Signals 120-160 ppm 200 180 20-0-075 160 240 120 80 40 20 100 pon
IR/HNMR/CNMR Unknown #25 MW-88 AMU Sp3 C-H 5,3 CH - Co- 6 ppm cha 3 .ca CH₂ - do 6 CH 3 180 150 140 120 100 rpm 80 60 40 20
Question1) identify the name of the compound represented on
the spectrum graph?
Question2) For CNMR, indicate how many types of carbon atoms
present and the identity of characteristics peaks?
Question3) For HNMR, indicate ho many types of carbon atoms
present, the different identity of characteristics peaks, and
explanations of it various splitting patterns?
Question4) Also for IR, indicate the identity of it
characteristics peaks
Question5) Finally for MS, Identify the parent peak, the
molecular weight and it implication, the most...
On the following pages you will find problems of both HNMR and
CNMR For each of the problems calculate the number of unsaturated
sites, each set of peaks are already labeled A,B, C…, darw the
proposed structure, and label the hydrogens appropriately. Example
provided. Line drawings are fine
Problem 7: CH20, U- 6122 δ 5.0, septet 82.3, q 6 1.3, d δ 1.2, t Draw structure and annotate BA 10 8 3 2 0 HSP-00-309 ppm Draw structure and annotate...
On the following pages you will find problems of both HNMR and
CNMR For each of the problems calculate the number of unsaturated
sites, each set of peaks are already labeled A,B, C…, darw the
proposed structure, and label the hydrogens appropriately. Example
provided. Line drawings are fine
Problem 2: C4HgO2 U- 511.5, s δ 2.3, t 81.8, multiplet δ 1.0, t Draw structure and annotate C B A 16 14 12 1O 6 4 2 0 4 HSP-00-115 ppm...
Part A: Make sure to write the labelled molecule structure on each 'HNMR and CNMR. Unknown #73: Annotate and assign the NMR Spectra of 5-chloro-2-pentanone: I m, 3H CH-CH2-CH2-CH - CH, m 3H m2H 11 10 9 8 7 6 5 1 HSP-00-414 ppm 10-09 Ci 6 b CH CH₂ CH₂ 1 1 CH₂ à el 1 СЕ О 60 40 200 200 180 160 140 120 100 30 ppm CDS-04-000
For the following unknown, annotate the corresponding spetras
and determine the molecular formula and lewis structure.
Unknown # s IR/HNMR/CNMR 1 MW= 88 AMU AVENUE S, 3 T, 1, 2] Broads, Ppm 200 160 140 180 120 80 40 60 20 ó 100 rpm
Using the HNMR, CNMR, IR, and mass spectroscopy given, identify
the unknown compound.
7.142 10 9 3 7 6 3 2 BC WAR 2S.b6 HS.7 45. 0 29 200 180 160 140 120 100 80 60 40 200 เ00 4000 2937 841197 41 639 9 t489 86 ほ67 86 100 MS-Nil-9551 80 60 40 20 0 S0 100 150 200 250 300 350