Draw the structures of Compound 13 a and 13b, clearly indicate your assignments of all proton resonances. Calculate the unsaturation index of each compound Compound 13a: C8H1002 A=7.17 ppm singlet 4h B=4.70 ppm singlet 4h C= 2.99 ppm singlet 2H 1)Excess CrO3, H2SO4 2) CH3OH (excess) , H+ heat Compound: C10H1004 A=8.11 ppm singlet 4H B=3.96 ppm singlet 6 H
Draw the structures of Compound 13 a and 13b, clearly indicate your assignments of all proton resonances. Calculate the unsaturation index of each compound Compound 13a: C8H1002 A=7.17 ppm singlet 4h B=4.70 ppm singlet 4h C= 2.99 ppm singlet 2H 1)Excess CrO3, H2SO4 2) CH3OH (excess) , H+ heat Compound: C10H1004 A=8.11 ppm singlet 4H B=3.96 ppm singlet 6 H
Chapter17: Alcohols And Phenols
Section17.SE: Something Extra
Problem 54AP: The 1HNMR spectrum shown is that of 3-methyl-3-buten-1-ol. Assign all the observed resonance peaks...
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![Draw the structures of Compound 13 a and 13b, clearly
indicate your assignments of all proton resonances.
Calculate the unsaturation index of each compound
Compound 13a: C8H1002
A=7.17 ppm singlet 4h
B=4.70 ppm singlet 4h
C= 2.99 ppm singlet 2H
1)Excess CrO3, H2SO4 2) CH3OH (excess) , H+ heat
Compound: C10H1004
A=8.11 ppm singlet 4H
B=3.96 ppm singlet 6 H](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F83bd02c6-d02f-4764-a848-15fcab9c3f4f%2Fea43d847-e45f-492f-8f80-90298ac5e936%2Fow0jd7e_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Draw the structures of Compound 13 a and 13b, clearly
indicate your assignments of all proton resonances.
Calculate the unsaturation index of each compound
Compound 13a: C8H1002
A=7.17 ppm singlet 4h
B=4.70 ppm singlet 4h
C= 2.99 ppm singlet 2H
1)Excess CrO3, H2SO4 2) CH3OH (excess) , H+ heat
Compound: C10H1004
A=8.11 ppm singlet 4H
B=3.96 ppm singlet 6 H
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