Chem 322 - Problem Set 6 - page 1
Note: You do not have to turn in this page. Just turn in page 2.
An unknown compound has the formula C10H10O3 and the spectra shown below.
Answer the questions on the following page about this compound and these spectra.

Chem 322 - Problem Set 6 - page 2
Due to Dr. Hietbrink by 3:00 on Monday 5-6-19.
Circle your class: MWF 11:15, MWF 12:20, TTh 2:00 Name _____________________ Class student # ____________
Score (out of 10) ____________
Answer these questions about the unknown compound C10H10O3 with spectra on the previous page.
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Hello my dear friend, i have also attached standard spectra of this compound with complete peak assignment especially for you! have a nice day!







Chem 322 - Problem Set 6 - page 1 Note: You do not have to turn in this page. Just turn in page 2. An unknown compound has the formula C10H10O3 and the spectra shown below. Answer the questions on the...
6. Spectroscopy. The molecular formula of an unknown organic compound is C8H1402. The IR, 1C-NMR and 'H-NMR spectra of this compound are shown on the next page. Answer the following questions about this compound. (a) What is the unsaturation number for this compound? (b) What functional group(s) does this compound contain? Indicate the specific evidence for your conclusion. (c) What can you conclude from the number of 13C-NMR signals? (d) What can you conclude from the H-NMR signal at 2.3...
In the boxes below, provide the structure of the compound that corresponds to each set of spectra on the next 5 pages. Be sure to show your work on the spectra for full credit. Account for all numbered peaks in the IR. In peaks if necessary. Assign all NMR spectra as completely as possible: number of NMR signals, integration, chemical shift, and splitting the mass spectrum, determine degrees of unsaturation and label 4 IR Spectrum 3000 2000 1 1600 1200...
The H-NMR spectrum of an unknown compound (formula CaHgO2) is shown below. Draw the structure of the unknown compound. Question 5 4 1 6 5 8 10 11 Ppm The 13C-NMR spectrum of an unknown compound (formula CgH180) is shown below. Its 1H-NMR spectrum only shows one singlet at 1.2 ppm. Draw the structure of this unknown compound. uestion 2 220 200 160 140 120 PPM 100 80 240 180 60 40 20 Create OscerSketch Answer 2 What would be...
3b. Analysis of FTIR, NMR Mass spectrum for Organic Unknown Compound. Below is the FTIR, 1H-NMR, 13C-NMR and Mass Spec data for an unknown compound. For each piece of information provided, write in the space below the figure the following for each spectra. What type of information is provided about the compound. Download the spectra (screen print) and mark up the spectra with what the signal represents as you determine the identity of this compound. Take a photo of your...
Problem set 2: (25 marks) In this problem you have to elucidate the structure of product B. A substrate A (structure shown in scheme 1) which was subjected to two consecutive reactions as shown in scheme 1 below to give the product B of molecular formula CsH14Br2. Provide the structure for Product B based on the NMR data provided (attachment 2: Problem set 2). (The 1H NMR and 13C NMR of starting substrate A has been provided for reference purpose...
formula: C10H12O2
determine structure given the IR and H NMR
Compound 2 Data Page Compound 2 Exact Mass: 164.0837 amu Compound 2 FTIR Compound 2 1H-NMR Coupling Pattern Coupling Constant, J (Hz) 10 Signal Chemical Shift Relative Integration (ppm) A 6.83 B 6. 82 1 C 6. 811 D 6 .291 1 E 6.049 1 F 5. 731 G3. 8123 J 1.830 3 Singlet Doublet Doublet Doublet of quartets Doublet of quartets Broad Singlet Singlet Doublet of Doublets Not determined...
6) The IR-, 1H- and 13C-spectra of an unknown sample having the formula C8H1602 are shown on the next page. a) What can you conclude about the structure form the 13C NMR data ? b) What functional group is present ? Explain your rational c) Propose a structure that is consistent with the spectroscopic data ? 8 8 3 3 8 3000 innn 500 400 2000 1500 Wavenumber[cm-11 TR2009-87586TK 13C NMR NB: solvent peaks have been edited out. 140 120...
Answer the following questions about the provided spectra: The Molecular Weight of the compound is 88 g/mol. A) (1 point) The broad peak at -3100 cm and the strong peak at 1700 cm' combined indicate the presence of what functional group? B) (1 point) How many hydrogen neighbors does the septet at 2.6 ppm in the 'H NMR spectrum have? C) (1 point) What functional group is indicated by the peak at 184 ppm in the C spectrum? D) (1...
General Note: If a printer is not accessible, the problem set may be completed on regular paper, but please ensure all answers are clear. Notations for IR and NMR may be written out and listed by wavenumbers and ppm, respectively. if this is the case or provided space is insufficient 1. (3 points) For the structure and 'H NMR spectrum shown below, match the labeled hydrogen atoms on the molecule (A-D) with the corresponding signals in the spectrum using the...
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...