A mass spectrum has an M+ peak at 170; and additional peaks at 127, 43, 29 and 15. Which of the following compounds could have produced this mass spectrum? iodoethane 2-iodopropane 1-chlorobutane 3-chloropentatne

A mass spectrum has an M+ peak at 170; and additional peaks at 127, 43, 29 and 15. Which of the following compounds could have produced this mass spectrum? iodoethane 2-iodopropane 1-chlorobutane 3-chloropentatne

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter13: Structure Determination: Nuclear Magnetic Resonance Spectroscopy

Section13.SE: Something Extra

Problem 59GP: The mass spectrum and 13C NMR spectrum of a hydrocarbon are shown. Propose a structure for this...

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Concept explainers

NMR Spectroscopy

NMR stands for Nuclear Magnetic Resonance in which the study of different molecules is done based on the interaction of radiofrequency electromagnetic radiations with the nuclei of molecules placed in a strong magnetic field. A precise study of spectra of visible light and all bands of electromagnetic radiation is called spectroscopy.

Question

A mass spectrum has an M+ peak at 170; and additional peaks at 127, 43, 29 and 15. Which of the following compounds could have produced this mass spectrum?

		iodoethane
		2-iodopropane
		1-chlorobutane
		3-chloropentatne

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