Determine the most likely structure of a compound with the formula C9H12 if it gave an H NMR spectrum consisting of:A doublet at d 1.25, a septet at d 2.90 and a multiplex at d 7.25 Determine the most likely structure of a compound, with the molecular formulaC₂H12, which gave a ¹H NMR spectrum consisting of:a doublet at d 1.25OOIOVONOIIIa septet at d 2.90 anda multiplet at d 7.25IV

Given, the 1H NMR data: a doublet at 1.25 a septet at 2.90 a multiplet at 7.25 We have to find the…

Determine the most likely structure of a compound, with the molecular formula C9H12, which gave a ¹H NMR spectrum consisting of: a doublet at d 1.25 Oll I OV OIV ||| a septet at d 2.90 and a multiplet at d 7.25 II III IV

Determine the most likely structure of a compound, with the molecular formula C9H12, which gave a ¹H NMR spectrum consisting of: a doublet at d 1.25 Oll I OV OIV ||| a septet at d 2.90 and a multiplet at d 7.25 II III IV

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter21: Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions

Section21.SE: Something Extra

Problem 80AP: Draw the structure of the compound that produced the spectra below. The infrared spectrum has strong...

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Mass Spectrometry

This process is an instrumental method in which a sample is changed to fast moving positive ions by electron bombardment. The charged particles vary due to their different mass to charge ratio and are estimated with the help of this difference. It is also called mass spectroscopy.

Question

Determine the most likely structure of a compound with the formula C9H12 if it gave an H NMR spectrum consisting of: A doublet at d 1.25, a septet at d 2.90 and a multiplex at d 7.25

Determine the most likely structure of a compound, with the molecular formula
C₂H12, which gave a ¹H NMR spectrum consisting of:
a doublet at d 1.25
O
O
I
OV
ON
OIII
a septet at d 2.90 and
a multiplet at d 7.25
IV

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