ATAR Notes: Forum
VCE Stuff => VCE Science => VCE Mathematics/Science/Technology => VCE Subjects + Help => VCE Chemistry => Topic started by: hyperblade01 on March 27, 2009, 08:04:25 pm
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Hey guys, today got a worksheet in class and unfortunately the teacher wasn't able to explain it well.
Basically there's an empty graph and we have to construct the NMR spectrum we would expect for X compound.
It says at the top a method on how to do it:
1. look up the chemical shft, place a line at the approximate value
2. Add the splitting information from adjacent H's
3. Add the intergration trace reflecting the number of H's in the group
I was hoping that someone would be able to explain/draw how 2-propanol and 1-chloro 2 methylpropane would look like on their respective graphs
Thanks in advance :)
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Keep in mind that protons closer to electronegative elements (oxygen) are more to the left.