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6. Provide at least one fragment (not the parent ion) that was useful in determining (or confirming) the structure...
10. Briefly explain how the 13C-NMR data was used to determine (or confirm your proposed structure....
10. Briefly explain how the 13C-NMR data was used to determine (or confirm your proposed structure. 11. In both of the boxes below, draw the bond-line structure with appropriate bond angles) of your unknown. On the structure on the left, indicate with a label (peak #from table above) and arrow the source of each signal. On the structure of the right, indicate with a label (13C-NMR ppm) and arrow the source of each signal. Chapter 5: INTEGRATED SPECTROSCOPY PROBLEMS 139...
8. Fill in the table below with the information on each unique 1H-NMR signal. You may treat all aromatic protons a...
8. Fill in the table below with the information on each unique 1H-NMR signal. You may treat all aromatic protons as a single signal if that helps. Peak # Chemical Shift (8) # of H Multiplicity Proposed Fragment Structure 9. Based on your molecular formula, 'H-NMR integration and 13C-NMR, is there any symmetry in your molecule? Explain. Chapter 5: INTEGRATED SPECTROSCOPY PROBLEMS 139 ompound 81 is a liquid (boiling point 85' C) that is commonly used as an aprotic solvent....
8. Give several pieces of data you gathered from the IR spectrum that aided in determining...
8. Give several pieces of data you gathered from the IR spectrum that aided in determining (or confirming) the structure of your unknown. For example, you might mention the presence (or absence) of certain definitive peaks (include wavenumbers). Do NOT use anything from the fingerprint region. 9. Fill in the table below with the information on each unique 1H-NMR signal. You may treat all aromatic protons as a single signal if that helps. Peak Chemical Shift (8) # of *10...
Please finish answering #3, 5 & 6 1. Show all your work for converting the elemental...
Please finish answering #3, 5 & 6
1. Show all your work for converting the elemental analysis data to a molecular formula, 53.31, 4.4315+2.214 ).71122 12 o107 11.13 11.019& 2.214 = 4.117- /2 1.00714 2.21142.2114( 2 )5, १११4 Cro back 2. Show all your work for calculating the degrees of unsaturation for your unknown. 1o 2N 2 4 2.4+2 3. What it the m/z value of the expected parent ion? Calculate the expected intensity of the [M+1] ion relative to...
5. Identify the base peak in your mass spectrum. 6. Are there other significant isotope patterns...
5. Identify the base peak in your mass spectrum. 6. Are there other significant isotope patterns in your mass spectrum? If so, what do they indicate? 7. Provide at least one fragment (not the parent ion) that was useful in determining (or confirming) the structure of the unknown and briefly explain how it was useful. Compound 14 is a liquid (b.p. 85") which finds its greatest application as an aprotic solvent UV-transparent; IR-liquid fim. MASS SPECTRAL DATA 99 100 Mass...
Unknown Number: Molecular Formula: Index of Hydrogen Deficiency: Structure: Mass Spec Molecular Weight: Important Fragments; what...
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...
Introduction One of the most important tasks that chemists are faced with is the separation and...
Introduction One of the most important tasks that chemists are faced with is the separation and identification of compounds from mixtures. Gratifyingly, chemists have multiple tools in the quest to identify unknown organic compounds. Infrared spectroscopy is useful for determining functional groups that may exist in a molecule. NMR spectroscopy tells information about the connectivity of C-H bonds, as well as the numbers of and chemical environments of both carbon and hydrogen (as well as many other NMR active nuclei,...
10. Briefly explain how the 13C-NMR data was used to determine (or confirm your proposed structure. 11. In both of the boxes below, draw the bond-line structure with appropriate bond angles) of your unknown. On the structure on the left, indicate with a label (peak #from table above) and arrow the source of each signal. On the structure of the right, indicate with a label (13C-NMR ppm) and arrow the source of each signal. Chapter 5: INTEGRATED SPECTROSCOPY PROBLEMS 139...
8. Fill in the table below with the information on each unique 1H-NMR signal. You may treat all aromatic protons as a single signal if that helps. Peak # Chemical Shift (8) # of H Multiplicity Proposed Fragment Structure 9. Based on your molecular formula, 'H-NMR integration and 13C-NMR, is there any symmetry in your molecule? Explain. Chapter 5: INTEGRATED SPECTROSCOPY PROBLEMS 139 ompound 81 is a liquid (boiling point 85' C) that is commonly used as an aprotic solvent....
8. Give several pieces of data you gathered from the IR spectrum that aided in determining (or confirming) the structure of your unknown. For example, you might mention the presence (or absence) of certain definitive peaks (include wavenumbers). Do NOT use anything from the fingerprint region. 9. Fill in the table below with the information on each unique 1H-NMR signal. You may treat all aromatic protons as a single signal if that helps. Peak Chemical Shift (8) # of *10...
Please finish answering #3, 5 & 6
1. Show all your work for converting the elemental analysis data to a molecular formula, 53.31, 4.4315+2.214 ).71122 12 o107 11.13 11.019& 2.214 = 4.117- /2 1.00714 2.21142.2114( 2 )5, १११4 Cro back 2. Show all your work for calculating the degrees of unsaturation for your unknown. 1o 2N 2 4 2.4+2 3. What it the m/z value of the expected parent ion? Calculate the expected intensity of the [M+1] ion relative to...
5. Identify the base peak in your mass spectrum. 6. Are there other significant isotope patterns in your mass spectrum? If so, what do they indicate? 7. Provide at least one fragment (not the parent ion) that was useful in determining (or confirming) the structure of the unknown and briefly explain how it was useful. Compound 14 is a liquid (b.p. 85") which finds its greatest application as an aprotic solvent UV-transparent; IR-liquid fim. MASS SPECTRAL DATA 99 100 Mass...
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...
Introduction One of the most important tasks that chemists are faced with is the separation and identification of compounds from mixtures. Gratifyingly, chemists have multiple tools in the quest to identify unknown organic compounds. Infrared spectroscopy is useful for determining functional groups that may exist in a molecule. NMR spectroscopy tells information about the connectivity of C-H bonds, as well as the numbers of and chemical environments of both carbon and hydrogen (as well as many other NMR active nuclei,...
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