سسسلا 4000 100 88898 80 IR Spectrum (CC solution) 60 29 mw 40 3000 13C NMR Spectrum (100.0 MM, CDCI, solution proton decoupled 10 9 DEPT CH CH CH 200 ¹H NMR Spectrum (200 MHz, CD, solution) MT - 88 2.0 80 120 8 2000 1 expansion 160 m/e 7 1744 V (am¹) 160 1600 1.0 200 120 1200 ppm 240 5 800 Mass Spectrum C4H802 280 solvent A 80 4 3 Problem 4 No significant UV Absorption abova 220 nm 40 2 0 1 8 (ppm) TMB 0 8 (ppm)
سسسلا 4000 100 88898 80 IR Spectrum (CC solution) 60 29 mw 40 3000 13C NMR Spectrum (100.0 MM, CDCI, solution proton decoupled 10 9 DEPT CH CH CH 200 ¹H NMR Spectrum (200 MHz, CD, solution) MT - 88 2.0 80 120 8 2000 1 expansion 160 m/e 7 1744 V (am¹) 160 1600 1.0 200 120 1200 ppm 240 5 800 Mass Spectrum C4H802 280 solvent A 80 4 3 Problem 4 No significant UV Absorption abova 220 nm 40 2 0 1 8 (ppm) TMB 0 8 (ppm)
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
ChapterL3: Carbon (13c) Nmr Spectroscopy
Section: Chapter Questions
Problem 9CTQ
Related questions
Question
Using this graph
The peak at 2.0 and 0.9 and 3.4 would be what? Singlet, doubler, triplet or quartet?
![100
80
4000
60
40
IR Spectrum
(CCle solution)
10
of base peak
29
40
3000
13C NMR Spectrum
(100.0 MHz, CDCI, solution
proton decoupled
9
57
DEPT CH CH₂ CH
200
¹H NMR Spectrum
(200 MHz, CD, solution)
MT-88
M₁
2.0
80
8
2000
120
expansion
mmm
160
7
m/e
1744
V (am¹)
160
1600
1.0
6
1200
120
C4H802
200 240 280
ppm
800
5
Mass Spectrum
solvent
1
80
|
3
Problem 4
No significant UV
absorption abowa 220 nm
40
2
1
0
8 (ppm)
TMS
L
0
8 (ppm)
10](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F24da4ca6-cf6f-4fa9-847a-91f16c4b9109%2Fa3a285f3-a595-4e6d-b47b-1fdb9e3244e6%2F9m1tw5r_processed.jpeg&w=3840&q=75)
Transcribed Image Text:100
80
4000
60
40
IR Spectrum
(CCle solution)
10
of base peak
29
40
3000
13C NMR Spectrum
(100.0 MHz, CDCI, solution
proton decoupled
9
57
DEPT CH CH₂ CH
200
¹H NMR Spectrum
(200 MHz, CD, solution)
MT-88
M₁
2.0
80
8
2000
120
expansion
mmm
160
7
m/e
1744
V (am¹)
160
1600
1.0
6
1200
120
C4H802
200 240 280
ppm
800
5
Mass Spectrum
solvent
1
80
|
3
Problem 4
No significant UV
absorption abowa 220 nm
40
2
1
0
8 (ppm)
TMS
L
0
8 (ppm)
10
Expert Solution
![](/static/compass_v2/shared-icons/check-mark.png)
This question has been solved!
Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.
Step by step
Solved in 3 steps with 2 images
![Blurred answer](/static/compass_v2/solution-images/blurred-answer.jpg)
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Recommended textbooks for you
![Organic Chemistry: A Guided Inquiry](https://www.bartleby.com/isbn_cover_images/9780618974122/9780618974122_smallCoverImage.gif)
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:
9780618974122
Author:
Andrei Straumanis
Publisher:
Cengage Learning
![Principles of Instrumental Analysis](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
![Organic Chemistry: A Guided Inquiry](https://www.bartleby.com/isbn_cover_images/9780618974122/9780618974122_smallCoverImage.gif)
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:
9780618974122
Author:
Andrei Straumanis
Publisher:
Cengage Learning
![Principles of Instrumental Analysis](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning