A compound containing Mn, CO and Cl shows peaks at 1950 cm-2000 cm -1 in IR spectrum. Mass spectral peaks were observed at = 404, 376, 348, 320, 292, 264, 236, 208, 180, 110, 55. Metastable peaks were observed at 349-1, 322 1, 294-3, 211, 183-3, 155-8, 67-2, 27-5. Suggest the most probable fragmentation pathway and predict the molecular structure.

A compound containing Mn, CO and Cl shows peaks at 1950 cm-2000 cm -1 in IR spectrum. Mass spectral peaks were observed at = 404, 376, 348, 320, 292, 264, 236, 208, 180, 110, 55. Metastable peaks were observed at 349-1, 322 1, 294-3, 211, 183-3, 155-8, 67-2, 27-5. Suggest the most probable fragmentation pathway and predict the molecular structure.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

Explain per step. Given the MS spectra below, show the fragmentation pattern responsible for m/z values.
Propose mechanisms for the formation of ion fragments m/z 97, 83, 69 and 55 in the mass spectrum of (CH3)2CCHC(O)C(CH3)2CHCH2 and explain in detail why this compound cannot undergo McLafferty rearrangement.
Identify, synthesized and show the mechanism show in the spectroscopy
Calculate the IHD and explain (elucidate) the structure using the 1H and 13C NMR data.
I. Butyramide (C4H9NO) 100 `NH2 80 20 10 20 30 40 50 60 70 80 90 m/z Identify the structure and provide the mechanism that give rise to the peak at m/z 59. Relative Intensity 우
Please help me with this, I am trying to prepare for my final exam next week and I am just completely lost
Interpret as many of the main peaks in the following spectra as you can – do this by providing the chemical formula of the species responsible for the peak in each case – you don’t need to outline specific fragmentation pathways, unless you want to! The structures of the chemicals are given to help you, as are a couple of the more obvious bond breakages. Need new solutions. Draw chemdraw computerised
Please provide the structure (drawing) given the IR and NMR spectra.
IR Spectrum and analysis of peaks Possible causes of error Discuss the mechanism and why a racemic mixture of cis and trans is formed
Kindly specify the absorption, appearance and compound for the ir spectra thanks!
k. N,N-diisopropylethylamine 100 80 60 40 20- 25 50 75 100 125 m/z Identify the structure that give rise to the peak at m/z 72 and 114. I. Butyramide (C4H9NO) 100- 'NH2 80 60 40 20 10 20 30 40 50 60 70 80 90 m/z Identify the structure and provide the mechanism that give rise to the peak at m/z 59. Relative Intensity Relative Intensity
Identify and draw the structure of the important peaks in the MS spectral data of C9H8O given below.