IR, HNMR, Mass Spec, CNMR Flashcards

1
Q

Br mass spec

A

m and m+2 peak same height

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

Cl mass spec

A

m and m+2 1/3 of eachother

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

C-C IR

A

1200

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

C=C IR

A

1660

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

c triple bond c IR

A

<2200

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

isolated C=C IR

A

1640-1680

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

conjugated c=c IR

A

1620-1640

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

aromatic IR

A

1600

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

sp3 c-h ir

A

2800-3000

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

c=c-h ir

A

3000-3100

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

c triple bond c-h

A

3300 sharp

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

oh ir

A

broad, rounded tip, 3300

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

r2nh ir

A

3300 broad with one sharp spike

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

rnh2 ir

A

broad with two sharp spikes

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

ketone c=o ir

A

1710

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

aldehyde c=o ir

A

1725, aldehyde 2700 2800 stretch

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

carboxylic acid ir

A

c=o is 1710 with broad oh

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

conjugated carbonyls ir

A

absorb at lower frequencies (1680)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

carbonyl amides ir

A

particularly low- 1640 to 1680

20
Q

carboxylic ester ir

A

1735

21
Q

strained cyclic ketones ir

A

highest frequency out of all; 1785

22
Q

c-n, c=n, cn ir

A

1200, 1660, >2200

23
Q

ir sulfure

A

m+2 peak larger than usual (4.2%)

24
Q

alkane hnmr

A

0.9

25
Q

alkane ch2 hnmr

A

1.3

26
Q

alkane ch hnmr

A

1.4

27
Q

methyl ketone hnmr

A

2.1

28
Q

acetylinic hnmr

A

2.5

29
Q

r-ch2-x hnmr

A

3-4

30
Q

c=c-h hnmr

A

5-6

31
Q

allylic h hnmr

A

1.7

32
Q

ph-h hnmr

A

7.2

33
Q

ph-ch3 hnmr

A

2.3

34
Q

aldehyde h hnmr

A

9-10

35
Q

carboxylic acid hnmr

A

10-12

36
Q

r-oh hnmr

A

10-12

37
Q

ar-oh hnmr

A

4-7

38
Q

r-nh2 hnmr

A

1.5-4

39
Q

n-h hnmr

A

3.5

40
Q

o-h hnmr

A

4.5

41
Q

coupling constants

A

-trans>cis>free rotation>geminal
ortho>allylic>meta

overall

trans,cis, ortho, free rotation, allylic, geminal=meta

42
Q

oh or nh on hnmr

A

will not show splitting if impure

43
Q

c=o cnmr

A

150-200

44
Q

c=c or aromatic c cnmr

A

100-150

45
Q

cnmr c-o or c triple bond c

A

50-100

46
Q

alkane cnmr

A

0-25

47
Q

c-cl or c-br cnmr

A

25-60