Finding the atomic makeup of a substance

  • Thread starter Thread starter PhiPhenomenon
  • Start date Start date
  • Tags Tags
    Atomic
Click For Summary
SUMMARY

This discussion focuses on the methods used to determine the atomic makeup and bonding structure of unknown substances, specifically highlighting techniques such as Mass Spectrometry (MS), Nuclear Magnetic Resonance (NMR), and various forms of spectroscopy. The user emphasizes the importance of MS for determining molar mass and bonding patterns, while also noting the utility of NMR for analyzing organic structures. Additionally, quick tests for functional groups can be performed using Infrared and UV-Vis spectroscopy. The conversation underscores the complexity and breadth of analytical chemistry techniques available for substance identification.

PREREQUISITES
  • Understanding of Mass Spectrometry (MS) techniques
  • Familiarity with Nuclear Magnetic Resonance (NMR) principles
  • Knowledge of various spectroscopy methods (e.g., Infrared, UV-Vis)
  • Basic chemistry concepts, including molecular structure and functional groups
NEXT STEPS
  • Research advanced Mass Spectrometry techniques, including tandem MS
  • Study the principles and applications of Nuclear Magnetic Resonance (NMR)
  • Explore different spectroscopy methods for functional group identification
  • Learn about the role of chemical shifts in NMR analysis
USEFUL FOR

Chemists, analytical scientists, and students transitioning into fields like neuroscience who are interested in substance identification and structural analysis techniques.

PhiPhenomenon
Messages
19
Reaction score
0
Hey all,

This is actually my first post on this forum but I have been reading it for a few months now.

Anyway, I'm sure the title of this thread might be confusing but this question has been bugging me for years now and I'm sure I'm missing something quite elementary. My question has to do with how exactly do people find the atomic makeup of an unknown substance and actually know enough to talk about it's bond structure.

For instance, I'm just imagining we have a bucket of ethenol (C2H4O1). I don't know what it is exactly and for all I know it could be just ethanol (C2H6O1) with a single sigma bond between the two carbons. How would I figure this out? For that matter, how do people know for certain that it is made up of carbon, oxygen and hydrogen?
 
Chemistry news on Phys.org
Besides many "wet" chemical tests that can be used to qualitatively identify functional groups and certain atoms (e.g., by precipitation, formation of colored derivatives, etc.), there is an entire field known as spectroscopy which encompasses a huuuuge range of test methods. To name a few: atomic emission spectroscopy, atomic absorption spectroscopy, UV-Vis, Fluoroescence/Chemiluminescence techniques, Mass spectrometry (this in itself is a huge field), Nuclear Magnetic Resonance (besides MS, this is the most powerful technique for determining organic structures), Infrared, Microwave, Raman, X-Ray diffraction, X-Ray Fluorescence, X-Ray Photoelectron Spectroscopy...

the list is massive and each technique gives certain information about a molecule. If I wanted to determine its molar mass, I would use Mass Spectrometry with a non-destructive ionization method. If I wanted to determine bonding patters, I would use MS with a destructive ionization pattern or better yet, something called tandem MS. Alternately, there is NMR, but that can be a finicky technique sometimes (but otherwise, it's EXTREMELY powerful, especially 2D or 3D pulse NMR experiments). For quick tests to look for functional groups, Infrared or UV-Vis would be a good technique. UV Vis could also tell me something about the orbital energies of a molecule (which is useful when looking at inorganic species).

Seriously, there are books and theses written about this and I can't even hope to touch on all the techniques! For Ethanol, though, I would perform a proton NMR experiment. It's very easy to analyze--you'd see 3 proton signals at different "chemical shifts." The peak height of the signal tells you about their relative ratios, so you'd see 3:2:1 relative peak heights. The specific chemical shift tells you the amount of electronic shielding against the applied magnetic field that is around each proton, and correspondingly, if it's attached to any heteroatoms, electron-donating, or electron-withdrawing groups.

It's a cool field :)
 
Wow, I actually understand that. Thank you! :)

I've been reading books on the subject for a while now. I'm actually fresh out of school with a BS in psychology (bleh!) and trying to transition into neuroscience.
 

Similar threads

Replies
6
Views
5K
Replies
3
Views
2K
Replies
1
Views
2K
  • · Replies 38 ·
2
Replies
38
Views
10K
Replies
3
Views
7K
  • · Replies 29 ·
Replies
29
Views
5K
  • · Replies 38 ·
2
Replies
38
Views
6K
  • · Replies 3 ·
Replies
3
Views
3K
  • · Replies 1 ·
Replies
1
Views
2K
  • · Replies 6 ·
Replies
6
Views
9K