15: Carbon NMR Flashcards

1
Q

What do the number of peaks on a carbon NMR spectrum show?

A

How many different carbon environments there are in a particular molecule

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1
Q

Why do carbons closer to more electronegative atoms have a higher chemical shift?

A

They are less shielded.

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2
Q

Name the solvent used in carbon NMR.

A

Tetramethylsilane

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3
Q

Give the formula for tetramethylsilane.

A

Si(CH3)4

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4
Q

Why do we use tetremetylsilane as the solvent in carbon NMR?

A

Its peak will form much further away from other molecules being analysed so does not interfere with the spectra

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5
Q

In proton NMR, what does the relative area under peaks represent?

A

The number of hydrogen atoms in each environment.

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6
Q

What is spin spin coupling?

A

Where clusters form on the spectrum rather than a single peak.
Help us identify the number of hydrogens on the neighbouring carbons.

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7
Q

What rule is spin spin coupling also known as?

A

n + 1

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8
Q

If a singlet is seen on a proton NMR spectrum, how many hydrogens would be seen on the adjacent carbons?

A

0

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9
Q

If a doublet is seen on a proton NMR spectrum, how many hydrogens would be seen on the adjacent carbons?

A

1

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10
Q

If a triplet is seen on a proton NMR spectrum, how many hydrogens would be seen on the adjacent carbons?

A

2

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11
Q

If a quartet is seen on a proton NMR spectrum, how many hydrogens would be seen on the adjacent carbons?

A

3

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12
Q

Why are proton free solvents needed in proton NMR?

A

So protons dont interfere with the spectrum.

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13
Q

What is another name for a proton free solvent?

A

Deuterated

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14
Q

Name 2 solvents that could be used in proton NMR.

A

CCl4 or Deuterium

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15
Q

What does the number of peaks on a proton NMR spectrum tell us?

A

How many different hydrogen environments there are in a compound.

16
Q

What does the ratio of peak areas on a proton NMR spectrum tell us?

A

The number of hydrogens in each environment

17
Q

What is the integration number?

A

The ratio of hydrogens in an environment represented by a peak.