Provide a structure for the compound C,H1,N, using the given information.IR: 3281 cm-1'H NMR: 8 1.1 (8H, t, J = 7 Hz), 8 2.66 (4H, q, J = 7 Hz), 8 2.83 (4H, s). (Hint: The triplet at & 1.1 conceals anotherbroad resonance that contributes to the integral.)

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Provide a structure for the compound C,H,N, using the given information. IR: 3281 cm-1 'H NMR: 8 1.1 (8H, t, J = 7 Hz), 8 2.66 (4H, q, J = 7 Hz), & 2.83 (4H, s). (Hint: The triplet at & 1.1 conceals another broad resonance that contributes to the integral.)

Provide a structure for the compound C,H,N, using the given information. IR: 3281 cm-1 'H NMR: 8 1.1 (8H, t, J = 7 Hz), 8 2.66 (4H, q, J = 7 Hz), & 2.83 (4H, s). (Hint: The triplet at & 1.1 conceals another broad resonance that contributes to the integral.)

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter12: Structure Determination: Mass Spectrometry And Infrared Spectroscopy

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Problem 49AP: The infrared spectrum of the compound with the mass spectrum shown below has a medium-intensity peak...

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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

Provide a structure for the compound C,H1,N, using the given information.
IR: 3281 cm-1
'H NMR: 8 1.1 (8H, t, J = 7 Hz), 8 2.66 (4H, q, J = 7 Hz), 8 2.83 (4H, s). (Hint: The triplet at & 1.1 conceals another
broad resonance that contributes to the integral.)

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