Spectroscopy Flashcards

1
Q

Nuclear Magnetic resonance principles

Peaks

A

Each peak on NMR spectroscopy represents hydrogens that are chemically equivalent

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2
Q

Nuclear Magnetic resonance principles

Calibration

A

NMR usually calibrated by a compound called TMS whose shift is at 0 ppm

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3
Q

Nuclear Magnetic resonance principles

Shielding

A

Shielding decreases with electron-withdrawing groups due to increasing influence of the magnetic field

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4
Q

Nuclear Magnetic resonance principles

Splitting

A

of peaks = (# of neighboring H within 3 bonds) + 1

Also called spin-spin coupling.
Adjacent hydrogens cause magnetic interference resulting in splitting of peaks on NMR spec.

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5
Q

Nuclear Magnetic resonance principles

Electron groups

A

Electron-donating groups increase shielding and are located more upfield (right).
Electron-withdrawing groups decrease shielding and are located more downfield (left).

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6
Q

Infrared spectroscopy peaks

C=O

range and peak shape

A

1750
Sharp

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7
Q

Infrared spectroscopy peaks

C=C

range and peak shape

A

1600-1680
Weak

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8
Q

Infrared spectroscopy peaks

C≡C or C≡N

range and peak shape

A

1900-2200
Medium

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9
Q

Infrared spectroscopy peaks

N-H

range and peak shape

A

3300
Sharp

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10
Q

Infrared spectroscopy peaks

O-H

range and peak shape

A

3000-3300
Broad

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11
Q

Nuclear Magnetic Resonance peaks

Shifts of Hydrogens of sp3 carbons

A

0 to 3

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12
Q

Nuclear Magnetic Resonance peaks

Shifts of Hydrogens of sp2 carbons

A

4.6 to 6

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13
Q

Nuclear Magnetic Resonance peaks

Shifts of Hydrogens of sp carbons

A

2 to 3

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14
Q

Nuclear Magnetic Resonance peaks

Shifts of Hydrogens of aromatics

A

6 to 8

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15
Q

Nuclear Magnetic Resonance peaks

Shifts of Aldehyde hydrogens

A

8 to 10

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16
Q

Nuclear Magnetic Resonance peaks

Shifts of -OH group hydrogens

A

1 to 5

17
Q

Nuclear Magnetic Resonance peaks

Shifts of Carboxylic acid hydrogens

A

10 to 12

18
Q

Mass Spectroscopy peaks

Molecular ion peak

A

Represents the molecule of interest

19
Q

Mass Spectroscopy peaks

Base peak

A

The tallest peak and represents the most abundant ion

20
Q

Mass Spectroscopy peaks

M+1 peak

A

A smaller peak to the right of the molecular ion peak.
Represents the abundance of carbon

21
Q

Mass Spectroscopy peaks

M+2 peak

A

Represents the abundance of Br or Cl

22
Q

Mass Spectroscopy peaks

m/z ratio

A

The x-axis represents the m/z ratio, or the ratio of mass to charge
Signal intensity represents the quantity of particles at a given m/z ratio

23
Q

Spectroscopy Types

Infrared spectroscopy

A

Based on absorption of infrared light and the principle that vibration or rotation of bonds causes a net change in dipole moment
Useful for determining functional groups

24
Q

Spectroscopy Types

Ultraviolet spectroscopy

A

Based on absorption of UV light, comparing absorption of a compound in a solvent with the reference as the solvent alone.
Most useful for conjugated π-bond systems

25
Q

Spectroscopy Types

Mass spectrometry

A

Mass spectrometry is based on electron collisions that result in ionization of compounds.
Used for determining molecular structure or weight of a compound.

26
Q

Spectroscopy Types

Nuclear magnetic resonance spectroscopy

A

Measures nuclear spin using a magnetic field.
Used for determining the functional groups of a compound.