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can you help with A b c d?
B Using the following analytical results, determine the...
im struggling trying to fogure out thos problem, help me? using the following analytical results, determine...
im
struggling trying to fogure out thos problem, help me? using the
following analytical results, determine the molecular structure of
compounds A, B, C, D:
Using the following analytical results, determine the molecular structure of compounds A, B, C, and D: Compound A has a molecular formula of C8H14. Compound A is oxidizable with peroxiacids to give a bicyclic product B. Ozonolysis of compound A followed by treatment with Zn/acetic acid resulted in compound C and formaldehyde (CH20). NMR and...
B (opts) (111) Using the following analytical results, determine the molecular structure of compounds A, B,...
B (opts) (111) Using the following analytical results, determine the molecular structure of compounds A, B, C, and D: Compound A has a molecular formula of CH. Compound A is oxidizable with peroxiacids to give a bieyelie product B. Ozonolysis of compound A followed by treatment with Zn/acetic acid resulted in compound C and formaldehyde (CH:0). NMR and IR analysis confirmed that compound C is ketone. a) Compound A b) Compound B c) Compound C 1. OSOs, pyidine d) Treatment...
B (Complete the following reactions by putting the structure of the missing compound or reagent in...
B (Complete the following reactions by putting the structure of the missing compound or reagent in the given box. Show stereochemistry clearly where applicable Bopas) 1. KMnO4 (1 2. + H₂O Na BH 3. 4. o CEC-chy Ly og 22, Acetic acid +Bel 6. Intermediate product BH THE the 7. ON peroxide a 8. + H Br hu 9. 10. OCCH), t.com heat CL 11. NOL Aceton B (LU) Using the following analytical results, determine the molecular structure of compounds...
Compound A (C11H16O) has a band in the IR spectrum at 3450 cm-1 (strong, broad) and...
Compound A (C11H16O) has a band in the IR spectrum at 3450 cm-1 (strong, broad) and does not react with pyridinium chlorochromate (PCC) in CH2CI2. Compound A does react with HBr to give compound B (11H15Br). Compound B reacts with potassium f-butoxide to give compound C (C11H14). Ozonolysis of C followed by treatment with Zn and water gives CH3CHO and compound D (C9H10O). The proton NMR spectrum of compound D is given below. Treatment of compound D with ethyl magnesium...
can you guys please explain #K. thank you a. The compounds that contains internal alkenes? and...
can you guys please explain #K. thank you
a. The compounds that contains internal alkenes? and b. The compound that forms an enolate when treated with base? e. The compound that forms a ketone upon treatment with H,SO/HO/Hgso? d. The compound that forms an aldehyde upon treatment with BH, followed by H,0, NaOH? e.The compound that is chiral? f. The compound that is 1-pentyne? g. The compound that contains sp-hybridized carbon? h. The compound that does not produce a diodide...
C. An organic compound A with molecular formula C:Hs0 shows a major peak at 1710 cm-'shows...
C. An organic compound A with molecular formula C:Hs0 shows a major peak at 1710 cm-'shows a positive Tollen's reagent test. When treated with NaBH. in THF, a compound B was obtained that showed IR peaks at 2920, 2850 cm-1 and a broad peak at 3300 cm and gave a negative Lucas test. Partial NMR data (not all peaks shown) of both A and B shows consistently 8 1.1(d, 6H) and 81.5 (m, 1H). Compound B when subjected to treatment...
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....
10. What is the major product of the following reaction? b. C. d. e. not a.-d....
10. What is the major product of the following reaction? b. C. d. e. not a.-d. 11. What ketone is formed from the reaction of the major product of the previous question with O and Zn? a. b. e. not a.-d.
21-Ketones are easily reduced to secondary alcohols. b- Primary CH, CCH, a-Secondary alcohol alcohol C- to...
21-Ketones are easily reduced to secondary alcohols. b- Primary CH, CCH, a-Secondary alcohol alcohol C- to acetaldehyde acid d-to carboxylic 22-Ozonolysis of alkenes yields aa-ketones if one of the unsaturated carbon atoms is disubstituted b-alcohol C-carboxylic acid d-alkane 23-Aldehyde C=0 is more polarized than ketone C-0 because a-As in carbocations, more alkyl groups stabilize + character b-Ketone has more alkyl groups, stabilizing the C=0 carbon inductively cc- due to a and b d- none of the above 24-Aldehydes and unhindered...
Please help me figure out what A,B, and C are! The bolded is what is provided...
Please help me figure out what A,B, and C are! The bolded is
what is provided by the prompt and my notes are the unbolded. IR
for Compound B and D shown.
Compound A, C7H14O2 did
not discharge precipitate in dilute permanganate solution or give a
precipitate with 2,4, DNP or with ceric nitrate.
2,4 DNP tests for aldehydes and ketones
Ceric nitrate tests for alcohols
Potassium Permanganate tests for double bonds
So compound A has 1 degree of unsaturation...
im
struggling trying to fogure out thos problem, help me? using the
following analytical results, determine the molecular structure of
compounds A, B, C, D:
Using the following analytical results, determine the molecular structure of compounds A, B, C, and D: Compound A has a molecular formula of C8H14. Compound A is oxidizable with peroxiacids to give a bicyclic product B. Ozonolysis of compound A followed by treatment with Zn/acetic acid resulted in compound C and formaldehyde (CH20). NMR and...
B (opts) (111) Using the following analytical results, determine the molecular structure of compounds A, B, C, and D: Compound A has a molecular formula of CH. Compound A is oxidizable with peroxiacids to give a bieyelie product B. Ozonolysis of compound A followed by treatment with Zn/acetic acid resulted in compound C and formaldehyde (CH:0). NMR and IR analysis confirmed that compound C is ketone. a) Compound A b) Compound B c) Compound C 1. OSOs, pyidine d) Treatment...
B (Complete the following reactions by putting the structure of the missing compound or reagent in the given box. Show stereochemistry clearly where applicable Bopas) 1. KMnO4 (1 2. + H₂O Na BH 3. 4. o CEC-chy Ly og 22, Acetic acid +Bel 6. Intermediate product BH THE the 7. ON peroxide a 8. + H Br hu 9. 10. OCCH), t.com heat CL 11. NOL Aceton B (LU) Using the following analytical results, determine the molecular structure of compounds...
Compound A (C11H16O) has a band in the IR spectrum at 3450 cm-1 (strong, broad) and does not react with pyridinium chlorochromate (PCC) in CH2CI2. Compound A does react with HBr to give compound B (11H15Br). Compound B reacts with potassium f-butoxide to give compound C (C11H14). Ozonolysis of C followed by treatment with Zn and water gives CH3CHO and compound D (C9H10O). The proton NMR spectrum of compound D is given below. Treatment of compound D with ethyl magnesium...
can you guys please explain #K. thank you
a. The compounds that contains internal alkenes? and b. The compound that forms an enolate when treated with base? e. The compound that forms a ketone upon treatment with H,SO/HO/Hgso? d. The compound that forms an aldehyde upon treatment with BH, followed by H,0, NaOH? e.The compound that is chiral? f. The compound that is 1-pentyne? g. The compound that contains sp-hybridized carbon? h. The compound that does not produce a diodide...
C. An organic compound A with molecular formula C:Hs0 shows a major peak at 1710 cm-'shows a positive Tollen's reagent test. When treated with NaBH. in THF, a compound B was obtained that showed IR peaks at 2920, 2850 cm-1 and a broad peak at 3300 cm and gave a negative Lucas test. Partial NMR data (not all peaks shown) of both A and B shows consistently 8 1.1(d, 6H) and 81.5 (m, 1H). Compound B when subjected to treatment...
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....
10. What is the major product of the following reaction? b. C. d. e. not a.-d. 11. What ketone is formed from the reaction of the major product of the previous question with O and Zn? a. b. e. not a.-d.
21-Ketones are easily reduced to secondary alcohols. b- Primary CH, CCH, a-Secondary alcohol alcohol C- to acetaldehyde acid d-to carboxylic 22-Ozonolysis of alkenes yields aa-ketones if one of the unsaturated carbon atoms is disubstituted b-alcohol C-carboxylic acid d-alkane 23-Aldehyde C=0 is more polarized than ketone C-0 because a-As in carbocations, more alkyl groups stabilize + character b-Ketone has more alkyl groups, stabilizing the C=0 carbon inductively cc- due to a and b d- none of the above 24-Aldehydes and unhindered...
Please help me figure out what A,B, and C are! The bolded is
what is provided by the prompt and my notes are the unbolded. IR
for Compound B and D shown.
Compound A, C7H14O2 did
not discharge precipitate in dilute permanganate solution or give a
precipitate with 2,4, DNP or with ceric nitrate.
2,4 DNP tests for aldehydes and ketones
Ceric nitrate tests for alcohols
Potassium Permanganate tests for double bonds
So compound A has 1 degree of unsaturation...
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