What is the primary reason Carbon-13 is used in NMR spectroscopy instead of Carbon-12?

Carbon-13 NMR Spectroscopy Concepts

Interactive Video
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Chemistry
•
11th - 12th Grade
•
Hard

Patricia Brown
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10 questions
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1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Carbon-12 is unstable in organic compounds.
Carbon-13 has an odd atomic mass, allowing for nuclear magnetic spin.
Carbon-13 is cheaper to produce.
Carbon-13 is more abundant than Carbon-12.
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
How is the chemical shift in a Carbon-13 NMR spectrum determined?
By comparing the frequency of the sample to a reference molecule.
By counting the number of hydrogen atoms.
By analyzing the color of the sample.
By measuring the temperature of the sample.
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
In a Carbon-13 NMR spectrum, what does the number of signals indicate?
The temperature at which the spectrum was recorded.
The molecular weight of the compound.
The number of different chemical environments for carbon atoms.
The number of hydrogen atoms in the molecule.
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Why is TMS commonly used as a reference molecule in Carbon-13 NMR?
It is highly reactive and interacts with the sample.
It has multiple chemical environments.
It is stable and has a single chemical environment.
It is the only available reference molecule.
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What does the presence of four signals in the Carbon-13 NMR spectrum of an ester indicate?
The ester is unstable.
The ester is composed of four different elements.
The ester has four different carbon chemical environments.
The ester has four hydrogen atoms.
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which carbon in an ester typically shows the highest chemical shift in a Carbon-13 NMR spectrum?
The carbon in a benzene ring.
The carbon in the carbonyl group.
The carbon connected to a methyl group.
The carbon connected to a hydroxyl group.
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
How many chemical environments are present in the molecule pentane?
Five
Four
Three
Two
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