NMR Flashcards

Understand NMR

1
Q

Xrays are scattered by atoms

A

we can measure the scattering pattern to tell us abput bond length and angles

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Radio waves make nuclei resonate

A

resonant frequencies tell us about the symmetry, connectivity of the hydrocarbon skeleton

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

IR waves make bonds vibrate

A

by plotting charts of absorption we can determine the functional groups in the molecule

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What does NMR do

A

it can tell the different proton environmentsand distinguish between the different protons

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what do the chemical shifts measure

A

the amount of shielding or deshileding around the proton

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

H atoms bonded to saturated carbons are where on the chemical shift?

A

right hand side, upfield, lower numbers, more shielded

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

H atoms bonded to electronegative atoms are where on the chemical shift?

A

downfield, to the left, higher numbers, deshielded

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is coupling?

A

protons interacting magnetically and can reveal the connectivity of the structure.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Where will CH3, CH2 and CH resonate?

A

CH3 are completely saturated and so resonate around 0.9. CH2 have 2 substituent atoms and thus resonate around 1.3 and CH at about 1.7

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

The intensity of the signal is…

A

generally proportion to th number of protons coming into resonance at the frequency of the signal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

The integration of the signal is…

A

the area under the absorption peak that is proportional to the number of protons being detected

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

The number of hydrogens on each peak represtented by the integration should…

A

add up to the total number of protons in the molecule

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

NMR and the inductive effect

A

The more alkyl groups you add onto a carbon, then the further downfield the molecule will be (downfield means a higher value)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Ainstropy of chemical bonds

A

chemical bonds are also regions of high electron density and if the field is sronger in one direction then the bond is ainstropic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Pi bonds and chemical shifts

A

pi bonds are especially effective in influencing the chemical shift of nearby atoms relative to their saturated counterparts

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

why use deuterated chlorform for H NMR?

A

because there is more solvent than product and if it is deuterated, it cuts out all the extra protons. 2H atoms have different properties and so dont show up on the spectra

17
Q

diastereoisomer and enantiomer definition

A

Diastereoisomer: stereoisomeric molecules that are not mirror images of each other but have swapped a substituient with another. Enantiomers are superimposable upon mirror image.