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Extra credit (2 pts) Draw a compound that would have an NMR that would consist of...
Question 4 3 pts The compound below would have signals in 1H-NMR andI signals in 13C-NMR....
Question 4 3 pts The compound below would have signals in 1H-NMR andI signals in 13C-NMR. Br ethyl 4-bromobutanoate
10. Which compound is likely to have the following 'H NMR spectrum (integration is not given)?...
10. Which compound is likely to have the following 'H NMR spectrum (integration is not given)? 64 Singlet 2 quartet 1 triplet a) CHOCH.CH c) CH3OQCH.CH d) CH3CH2CCH.CH 11. Compound W has the formula CsH10. a) How many units of unsaturation does w have? Show your work b) The 'H NMR spectrum has the following signals: 1 H a 9.5 singlet 9H a 1.0 singlet What is the structure of W? Partial credit for anything you can say about the...
Draw a compound with the formula C6H12 that would show exactly two signals in its 13C-NMR...
Draw a compound with the formula C6H12 that would show exactly two signals in its 13C-NMR spectrum.
PART 2 Draw the most accurate 'H-NMR spectrum you can for the following molecules. Show all...
PART 2 Draw the most accurate 'H-NMR spectrum you can for the following molecules. Show all signals including an accurate representation of splitting, intensity and position. Assume no signal overlap (i.e. if you expect signals have similar chemical shifts, just place them next to each other). Clearly label the integration value for each signal. Indicate the correlation between each proton (HA, HB, etc) and each signal (label signals A, B, etc.) ppm 12.5 10 11 O ppm 12.5 10 ii...
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the...
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. он ethanol OH 4-methylheptan-4-ol
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the f...
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. OH ethanol OH 4-methylheptan-4-ol
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the f...
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. OH ethanol OH 4-methylheptan-4-ol
5 points How many 1H NMR signals would you expect from this compound? СІ 1 -0....
5 points How many 1H NMR signals would you expect from this compound? СІ 1 -0. Type your answer... 2 5 points How many ?H NMR signals would you expect from this compound? OH Type your answer... Question 3 The structure below has three IH NMR signals with chemical shifts list "a", "b", and "c". The H atoms in the structure below are labeled "1)", "2)
The^1H-NMR of a compound with molecular formula C_7H_15CI consists of two signals: 1.1 (singlet, integrating to...
The^1H-NMR of a compound with molecular formula C_7H_15CI consists of two signals: 1.1 (singlet, integrating to 9 Hydrogen's) and 1.6 (singlet, integrating to 6 Hydrogen's). Propose a structural formula for this compound consistent with this information. You do not have to consider stereochemistry. You do not have to explicitly draw II atoms.
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how...
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. OH ethanol 4-methylheptan-4-01
Question 4 3 pts The compound below would have signals in 1H-NMR andI signals in 13C-NMR. Br ethyl 4-bromobutanoate
10. Which compound is likely to have the following 'H NMR spectrum (integration is not given)? 64 Singlet 2 quartet 1 triplet a) CHOCH.CH c) CH3OQCH.CH d) CH3CH2CCH.CH 11. Compound W has the formula CsH10. a) How many units of unsaturation does w have? Show your work b) The 'H NMR spectrum has the following signals: 1 H a 9.5 singlet 9H a 1.0 singlet What is the structure of W? Partial credit for anything you can say about the...
PART 2 Draw the most accurate 'H-NMR spectrum you can for the following molecules. Show all signals including an accurate representation of splitting, intensity and position. Assume no signal overlap (i.e. if you expect signals have similar chemical shifts, just place them next to each other). Clearly label the integration value for each signal. Indicate the correlation between each proton (HA, HB, etc) and each signal (label signals A, B, etc.) ppm 12.5 10 11 O ppm 12.5 10 ii...
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. он ethanol OH 4-methylheptan-4-ol
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. OH ethanol OH 4-methylheptan-4-ol
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. OH ethanol OH 4-methylheptan-4-ol
5 points How many 1H NMR signals would you expect from this compound? СІ 1 -0. Type your answer... 2 5 points How many ?H NMR signals would you expect from this compound? OH Type your answer... Question 3 The structure below has three IH NMR signals with chemical shifts list "a", "b", and "c". The H atoms in the structure below are labeled "1)", "2)
The^1H-NMR of a compound with molecular formula C_7H_15CI consists of two signals: 1.1 (singlet, integrating to 9 Hydrogen's) and 1.6 (singlet, integrating to 6 Hydrogen's). Propose a structural formula for this compound consistent with this information. You do not have to consider stereochemistry. You do not have to explicitly draw II atoms.
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. OH ethanol 4-methylheptan-4-01
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