1/13
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai |
|---|
No analytics yet
Send a link to your students to track their progress
Chemical Shift
location of signal (ppm) on x-axis
gets more info on environment of proton
Integration
Number of protons being represented by the signal
will add up to Hs in compound
Splitting Pattern
Shape of signal
Downfield/ Downshielded
Experiences a magnetic field that is more than the instrument
closer to electronegative atoms and electron density
Upfield/ Shielded
Experiences a magnetic field that is less than the instrument
TMS
Internal Standard = 0 ppm
not part of the compound being analyzed
Monosubstituted Rings
integration of 5Hs in aromatic region
ideally has 3 signals - but overlaps so looks like one signal
Disubstituted Ring
integration of 4Hs in aromatic region
has 2 substitutions on ring (A and B)
3 Options
“ortho” option
4 signals
Each signal integrating for H
2 doublets (dd)
2 triplets (tt)
“meta” option
4 signals
Each signal integrating for H
2 doublets (dd)
1 triplet (t)
1 singlet (s)
“para” option
2 signals
Each signal integrating for 2Hs
Complex Splitting
Using more sensitive instrument/stronger magnet to differentiate types of neighbors in a splitting pattern.
H2O Exhange
will exchange with acidic Hs
OH
Carboxylic Acids
amines/amides
dissolves in a deuterated solvent, which replaces an H
Deuterated Solvent
Solvents that are isotopes of H are used to ensure that we are seeing signals from ONLY our compound in HNMR.