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4. Write in the product of this reaction: LiAlH4 N=CCHCH2CH3 CH3 5. Which type of spectroscopy (IR, 'H NMR, and/or ''C...
4. Write in the product of this reaction: LiAlH4 N=CCHCH2CH3 CH3 5. Which type of spectroscopy...
4. Write in the product of this reaction: LiAlH4 N=CCHCH2CH3 CH3 5. Which type of spectroscopy (IR, 'H NMR, and/or ''C NMR) would be good to distinguish between benzoic acid and acetonitrile? State what you would observe for each compound in each type of spectroscopy and whether that type of spectroscopy would be a good way to distinguish between the two compounds. acetonitrile benzuicacle 13C NMR
OCH3 4. Write in the product of this reaction: LiAlH4 N=CCHCH2CH2OH CH; 5. Which type of...
OCH3 4. Write in the product of this reaction: LiAlH4 N=CCHCH2CH2OH CH; 5. Which type of spectroscopy (IR, 'H NMR, and/or C NMR) would be good to distinguish between ethanol and acetonitrile? State what you would observe for each compound in each type of spectroscopy and whether that type of spectroscopy would be a good way to distinguish between the two compounds.
please answer #5 5. Which type of spectroscopy (IR, 'H NMR, and/or "C NMR) would be good to distinguish between prop...
please answer #5
5. Which type of spectroscopy (IR, 'H NMR, and/or "C NMR) would be good to distinguish between propanal and propanoic acid? State what you would observe for each compound in each type of spectroscopy and whether that type of spectroscopy would be a good way to distinguish between the two compounds.
3. Which type of spectroscopy (IR, 'H NMR, and/or C NMR) would be good to distinguish...
3. Which type of spectroscopy (IR, 'H NMR, and/or C NMR) would be good to distinguish between acetone and 2-propanol? State what you would observe for each compound in each type of spectroscopy and whether that type of spectroscopy would be a good way to distinguish between the two compounds.
1. Name this compound, including stereochemistry: HOCCECCH,CH Show the step(s) necessary to transform the compound...
1. Name this compound, including stereochemistry: HOCCECCH,CH Show the step(s) necessary to transform the compound on the left into the acid on the right. chlorobenzene benzoic acid 3. What are the products of the following reaction? H:0* 4. Write in the product of this reaction: H2O C6H5CH2C=N ------ H. heat 5. Which type of spectroscopy (IR, 'H NMR, and/or SC NMR) would be good to distinguish between acetonitrile and acetic acid? State what you would observe for each compound in...
#1-5. Dr. Hellwig OMEWORK 5 Chem 204 Name this compound, including stereochemistry: 1. cCoCt носс-сСH,ОСHS 2....
#1-5.
Dr. Hellwig OMEWORK 5 Chem 204 Name this compound, including stereochemistry: 1. cCoCt носс-сСH,ОСHS 2. Show the step(s) necessary to transform the compound on the left into the acid on the right. m-methoxytoluene m-methoxybenzoic acid 3. What are the products of the following reaction? Но" Write in the product of this reaction: 4 Н.о H2C=CHCH2C N H', heat 5. Which type of spectroscopy (IR, 'H NMR, and/or C NMR) would be good to distinguish between acetonitrile and benzoic acid?...
please answer 3,4 & 5 3. What are the products of the following reaction? H30* CH2O...
please answer 3,4 & 5
3. What are the products of the following reaction? H30* CH2O 4. Write in the product of this reaction: H30* N=CCHCH2C6H5 OCH heat 5. Which type of spectroscopy (IR, 'H NMR, and/or C NMR) would be good to distinguish between propanal and propanoic acid? State what you would observe for each compound in each type of spectroscopy and whether that type of spectroscopy would be a good way to distinguish between the two compounds.
3. (6 points) How could spectroscopy (IR, 'H NMR and/or 3C NMR) be used to distinguish...
3. (6 points) How could spectroscopy (IR, 'H NMR and/or 3C NMR) be used to distinguish between the following pair of compounds? a. (CH3)3N and CH3NHCH2CH3 and
draw chlorination Mechanism faw Yhe chlorinahion mathenism and the other a ketone, is: A) 13C NMR B) 'H NMR C) Mass spectroscopy D IR spectroscopy E) UV/VIS spectroscopy 23. The last step in t...
draw chlorination Mechanism
faw Yhe chlorinahion mathenism and the other a ketone, is: A) 13C NMR B) 'H NMR C) Mass spectroscopy D IR spectroscopy E) UV/VIS spectroscopy 23. The last step in the chlorination of an aromatic ring is: A) Formation of the Wheland intermediate B) Attack of the benzene ring onto the polarized chlorine molecule C) Lewis acid-Lewis base reaction D) Deprotonation of the Wheland intermediate E) Addition of the chlorine atom to the sp hybridized carbon 24....
7. Compounds 4 and 5, both of which have the formula CsH9N, and the IR/13C NMR...
7. Compounds 4 and 5, both of which have the formula CsH9N, and the IR/13C NMR that follows show up in this reaction scheme. What structures are they? (No lone pairs are shown for options, but all are neutral). Nacy NaNH2 NO RXN SANH anion of 5 (+NH3) + Nal FTIR 13C 5 C CH CH2 CH3 100 80 60 40z pom NH2 c -CEN コミュー H-N A) 4, 5 B) 4, 5 C) 4, 5
4. Write in the product of this reaction: LiAlH4 N=CCHCH2CH3 CH3 5. Which type of spectroscopy (IR, 'H NMR, and/or ''C NMR) would be good to distinguish between benzoic acid and acetonitrile? State what you would observe for each compound in each type of spectroscopy and whether that type of spectroscopy would be a good way to distinguish between the two compounds. acetonitrile benzuicacle 13C NMR
OCH3 4. Write in the product of this reaction: LiAlH4 N=CCHCH2CH2OH CH; 5. Which type of spectroscopy (IR, 'H NMR, and/or C NMR) would be good to distinguish between ethanol and acetonitrile? State what you would observe for each compound in each type of spectroscopy and whether that type of spectroscopy would be a good way to distinguish between the two compounds.
please answer #5
5. Which type of spectroscopy (IR, 'H NMR, and/or "C NMR) would be good to distinguish between propanal and propanoic acid? State what you would observe for each compound in each type of spectroscopy and whether that type of spectroscopy would be a good way to distinguish between the two compounds.
3. Which type of spectroscopy (IR, 'H NMR, and/or C NMR) would be good to distinguish between acetone and 2-propanol? State what you would observe for each compound in each type of spectroscopy and whether that type of spectroscopy would be a good way to distinguish between the two compounds.
1. Name this compound, including stereochemistry: HOCCECCH,CH Show the step(s) necessary to transform the compound on the left into the acid on the right. chlorobenzene benzoic acid 3. What are the products of the following reaction? H:0* 4. Write in the product of this reaction: H2O C6H5CH2C=N ------ H. heat 5. Which type of spectroscopy (IR, 'H NMR, and/or SC NMR) would be good to distinguish between acetonitrile and acetic acid? State what you would observe for each compound in...
#1-5.
Dr. Hellwig OMEWORK 5 Chem 204 Name this compound, including stereochemistry: 1. cCoCt носс-сСH,ОСHS 2. Show the step(s) necessary to transform the compound on the left into the acid on the right. m-methoxytoluene m-methoxybenzoic acid 3. What are the products of the following reaction? Но" Write in the product of this reaction: 4 Н.о H2C=CHCH2C N H', heat 5. Which type of spectroscopy (IR, 'H NMR, and/or C NMR) would be good to distinguish between acetonitrile and benzoic acid?...
please answer 3,4 & 5
3. What are the products of the following reaction? H30* CH2O 4. Write in the product of this reaction: H30* N=CCHCH2C6H5 OCH heat 5. Which type of spectroscopy (IR, 'H NMR, and/or C NMR) would be good to distinguish between propanal and propanoic acid? State what you would observe for each compound in each type of spectroscopy and whether that type of spectroscopy would be a good way to distinguish between the two compounds.
3. (6 points) How could spectroscopy (IR, 'H NMR and/or 3C NMR) be used to distinguish between the following pair of compounds? a. (CH3)3N and CH3NHCH2CH3 and
draw chlorination Mechanism
faw Yhe chlorinahion mathenism and the other a ketone, is: A) 13C NMR B) 'H NMR C) Mass spectroscopy D IR spectroscopy E) UV/VIS spectroscopy 23. The last step in the chlorination of an aromatic ring is: A) Formation of the Wheland intermediate B) Attack of the benzene ring onto the polarized chlorine molecule C) Lewis acid-Lewis base reaction D) Deprotonation of the Wheland intermediate E) Addition of the chlorine atom to the sp hybridized carbon 24....
7. Compounds 4 and 5, both of which have the formula CsH9N, and the IR/13C NMR that follows show up in this reaction scheme. What structures are they? (No lone pairs are shown for options, but all are neutral). Nacy NaNH2 NO RXN SANH anion of 5 (+NH3) + Nal FTIR 13C 5 C CH CH2 CH3 100 80 60 40z pom NH2 c -CEN コミュー H-N A) 4, 5 B) 4, 5 C) 4, 5
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