Save
Chemistry
Organic 2
NMR spectroscopy
Save
Share
Learn
Content
Leaderboard
Share
Learn
Created by
Lucy
Visit profile
Cards (25)
What is NMR spectroscopy used for?
It is used to determine the structure of a molecule.
View source
How does NMR spectroscopy analyze bond environments?
It analyzes the energy absorbed by different bond environments.
View source
What does each peak in an NMR spectrum represent?
Each peak represents a different bond environment within the molecule.
View source
What is the standard molecule used in NMR spectroscopy?
Tetramethylsilane (TMS) is the standard molecule.
View source
Why is TMS considered a standard molecule in NMR?
It contains four identical carbon and hydrogen environments.
View source
At what value does TMS appear on the NMR spectrum?
TMS appears at
∂=0
ppm
on the x-axis.
View source
What does C<sup>13</sup> NMR analyze?
C<sup>13</sup> NMR analyzes the different
carbon environments
in a molecule.
View source
How do carbon environments near oxygen behave in C<sup>13</sup> NMR?
They have
∂ values
that are shifted to the
right
.
View source
Why might a molecule with symmetry display fewer ∂ peaks than carbon atoms?
Symmetry can cause multiple carbon atoms to have the same
environment
.
View source
How many carbon atoms does 1,2-cyclohexanediol contain?
It contains
six
carbon atoms.
View source
How many peaks does the NMR spectrum of 1,2-cyclohexanediol show?
It shows three peaks due to the symmetry of the molecule.
View source
What does H<sup>1</sup> NMR analyze?
H<sup>1</sup> NMR analyzes the different
hydrogen
environments
in a molecule.
View source
What must samples be dissolved in for H<sup>1</sup> NMR analysis?
They must be dissolved in a
non-hydrogen-containing
solvent.
View source
What is a common solvent used in H<sup>1</sup> NMR?
CCl<sub>4</sub> is a common solvent used.
View source
Why are H<sup>1</sup> NMR spectra more complex than C<sup>13</sup> spectra?
Because the heights of the
peaks
show the relative intensity of each
∂ value
.
View source
What do the heights of the peaks in H<sup>1</sup> NMR correspond to?
They correspond to the number of hydrogens in that certain environment.
View source
What does the splitting pattern in H<sup>1</sup> NMR indicate?
It indicates how many hydrogens are on the adjacent carbon atom.
View source
What is the 'n+1' rule in NMR spectroscopy?
The 'n+1' rule states that n is the number of hydrogens on the adjacent carbon.
View source
What does a singlet indicate in H<sup>1</sup> NMR?
A singlet indicates no
hydrogens
on the adjacent
carbon
.
View source
What does a doublet indicate in H<sup>1</sup> NMR?
A doublet indicates one
hydrogen
on the adjacent
carbon
.
View source
What does a triplet indicate in H<sup>1</sup> NMR?
A triplet indicates two
hydrogens
on the adjacent
carbon
.
View source
What does a quartet indicate in H<sup>1</sup> NMR?
A quartet indicates three
hydrogens
on the adjacent
carbon
.
View source
What is a common splitting pattern in H<sup>1</sup> NMR?
A
triplet-quartet
splitting pattern is a common combination.
View source
What does the triplet-quartet splitting pattern represent?
It represents a -
CH<sub>2</sub>
-
CH<sub>3</sub>
fragment.
View source
How can multiple fragments be used in NMR spectroscopy?
They can be pieced together to determine the full molecule structure.
Each fragment corresponds to a
specific
splitting pattern
.
View source