Shown below is the ¹H-NMR spectrum of a compound with the formula C5H10O2. 2H Peak Splitting quartet quartet triplet triplet 1 2 3 4 a b c d e a b CH3CH₂CH₂CH₂COH 2 A 2H PPM Choose from the constitutional isomers below to assign a structure to this spectrum. O B d CH3CH₂CH₂COCH3 3 3H 4 3H a b || c CH3CH₂COCH₂CH3 C (Choose the letter corresponding to the correct structure from the drop-down list provided.) Correct Structure: C Assign signal number 3 (indicated as a red number on the spectrum above) to its corresponding hydrogen(s) (shown as a red lower-case letter on the structure above). (Write the letter of the hydrogen (or set of equivalent hydrogens) in the box provided, e.g., a) Signal number 3 corresponds to hydrogen(s): Previous Next
Shown below is the ¹H-NMR spectrum of a compound with the formula C5H10O2. 2H Peak Splitting quartet quartet triplet triplet 1 2 3 4 a b c d e a b CH3CH₂CH₂CH₂COH 2 A 2H PPM Choose from the constitutional isomers below to assign a structure to this spectrum. O B d CH3CH₂CH₂COCH3 3 3H 4 3H a b || c CH3CH₂COCH₂CH3 C (Choose the letter corresponding to the correct structure from the drop-down list provided.) Correct Structure: C Assign signal number 3 (indicated as a red number on the spectrum above) to its corresponding hydrogen(s) (shown as a red lower-case letter on the structure above). (Write the letter of the hydrogen (or set of equivalent hydrogens) in the box provided, e.g., a) Signal number 3 corresponds to hydrogen(s): Previous Next
Chapter17: Alcohols And Phenols
Section17.11: Spectroscopy Of Alcohols And Phenols
Problem 19P: When the 1HNMR spectrum of an alcohol is run in dimethylsulfoxide (DMSO) solvent rather than in...
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