I have most of the information, but I need help to organize it based on the prompts below the pictures.
Mass Spec
Molecular Weight:
Important Fragments; what are they and what do they mean? (base peak structure, is there a halogen, is there a benzene ring, is there an odd number of nitrogens, other important fragments that tell something about the structure)
IR
Is there an OH? Wavenumber?
Is there a carbonyl group? If so what type (acid. ester, amide, aldehyde, ketone etc.)? Wave number?
Other important peaks (terminal alkyne, cyano group, aromatic, alkene, nitro group, amine etc.) and where are they?
1H-NMR
Identify every signal; chemical shift, what is it due to( i.e what type of proton, aromatic, aldehydic, O-H, N-H, vinyl etc.) and how many protons does it represent.
13C-NMR
How many different types of carbons are present?
What type of carbon does each signal represent?
How can you put the skeleton together?
LOGIC:
Carefully, and thoroughly show how you used the spectral data to determine your structure. Show how all your data confirms your structure. Especially useful is using 1H-NMR as confirmation.
I have most of the information, but I need help to organize it based on the...
I need to know what the unknown compound is and what the structure looks like based off this H-NMR chart, IR peak and Molecular Formula. Can you please draw the structure out so I can see it. I also want to see how the peaks on the H-NMR relate to the compound you have drawn (like which peak goes to what point on the compond).Hint something that would be leaking out of an oil sands talings pond, also the molecule...
Organic Chemistry - Using the following IR anaylsis identify the major peaks and possible functional group identity. Using the two NMR spectra, discuss the integration of peaks, chemical shifts, and splitting. Using the mass spectra, identify molecular weight and important fragments to confirm the structure. Draw the fragments that correspond to each peak in the mass spectra. Draw the structure of the unknown that corresponds to all available data. additional information: Unknown ‘J’ is a alkane. H-NMR multiplet, 1OH triplet,...
Provide the correct structure for your unknown based on the spectroscopic data provided. Provide the correct name for your compound. Either the IUPAC name, or a commonly accepted name (i.e., ethyl acetate in place of ethyl ethanoate) will be accepted.IR spectrum: Assign as many peaks as possible. In particular, you should assign peaks that were important in making your structural interpretation (i.e. functional group peaks such as OH, C=O, N-H, etc.). 1H-NMR spectrum: Assign all the peaks in the spectrum...
Unknown Number: Molecular Formula: Index of Hydrogen Deficiency: Structure: Mass Spec Molecular Weight: Important Fragments; what are they and what do they mean? (base peak structure, is there a halogen, is there a benzene ring, is there an odd number of nitrogens, other important fragments that tell something about the structure) IR Is there an OH? Wavenumber? Is there a carbonyl group? If so what type (acid. ester, amide, aldehyde, ketone etc.)? Wave number? Other important peaks (terminal alkyne, cyano...
IR List the important peaks seen in the IR of the product and label with the associated stretches and bends (eg. C-H stretch, etc). 13C NMR List all the peaks in the 13C NMR and give them each a number. Write the structure of the product and label the carbons with the associated number for the peak. (The peaks from 21-25 can be given the same number.) 1H NMR List all the peaks in the 1H NMR and give them...
I have an proton NMR for a compound that I believe to be Salicylic Acid. It has major peaks at 11.0 ppm as well as around 10.5 ppm. Both peaks are broad singlets indicating that they should be -OH peaks. However, the typical Phenol has a peak around 5-6 ppm. Could it be possible that the aromatic ring and carbonyl group from the carboxylic acid influenced the phenol group enough to shift it that far downfield?
Identify the unknown molecule based on the following information Formula: CisHasNO IR peaks (cm): 3423 (broad), 3350 (overlap), 1728 (strong), 1585 (weak) Mass Spec: base peak (m/2) - 136 UV-Vis - 379 nm (benzene - 255 nm) 13C: 8 186, 157, 155, 153, 150, 148, 147, 145, 143, 142, 139, 138, 135, 56, 52 "H: 8 13.11 (s, 1H), 9.94 (s, 1H, broad), 8.21 (d, 1H), 8.04 (d, 1H), 7.75 dd, 1H), 7.32 (dd, 1H), 7.05 (dd, 1H), 7.03 (d,...
please help me with this. I am not good at reading the IR charts. Spectroscopid Analysuts 호 Prot, Zuhncky deoded io analyse a whaleystaline solid left behind by a student one aftomoon. By using mass spectrometry, be igured out that the molecular weight or the axilpound wins 70 밂mol. Prot Zuhncky also n and obtained the folkowing IR and 1H-NMR spectra. Based on this nformation, determine the structure of this unknown by determining the moleculsr formula first them determining the...
please help me answer the IR, H NMR and 13C NMR questions based on the pictures below. IR List the important peaks seen in the IR of the product and label with the associated stretches and bends (eg. C-H stretch, etc). 13C NMR List all the peaks in the 13C NMR and give them each a number. Write the structure of the product and label the carbons with the associated number for the peak. (The peaks from 21-25 can be...
On the following pages are two problems. You have a molecular formula, an IR, a 1H NMR and a 13C NMR. For each problem: a. (1 pt) Calculate the index of hydrogen deficiency. b. (4 pts) Propose a structure that is consistent with the spectra. c. (1 pt) Indicate the important peaks in the IR and what features in your structure they correlate to. (Ignore the fingerprint region.) Keep in mind that the IR can sometimes be confusing. d. (2...