Provide rational interpretation of all the spectral data given below to determine the structures of the corresponding compounds. IR Spectrum 4000 100 woteps 3000 40 10 13C NMR Spectrum (900 MHE. COO, soton BO proton decoupled 200 DEPT Oui ont cHt H NMR Spectrum (200 M, CDC, solution) 2000 120 v (om 160 m/e 160 трудотуу 1200 1600 100-300 200 ele 120 Mass Spectrum C₂H₁₁Br 280 240 Resvesno 800 Resolves in 80 ppm 1.0 ang 200 Problem 91 40 UV spectrum 5.30 path leng solvere d 300 250 λ (nm) 0 350 & (ppm) TMIS O 8 (ppm)
Provide rational interpretation of all the spectral data given below to determine the structures of the corresponding compounds. IR Spectrum 4000 100 woteps 3000 40 10 13C NMR Spectrum (900 MHE. COO, soton BO proton decoupled 200 DEPT Oui ont cHt H NMR Spectrum (200 M, CDC, solution) 2000 120 v (om 160 m/e 160 трудотуу 1200 1600 100-300 200 ele 120 Mass Spectrum C₂H₁₁Br 280 240 Resvesno 800 Resolves in 80 ppm 1.0 ang 200 Problem 91 40 UV spectrum 5.30 path leng solvere d 300 250 λ (nm) 0 350 & (ppm) TMIS O 8 (ppm)
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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
Transcribed Image Text:Provide rational interpretation of all the spectral data given below to determine the structures of the
corresponding compounds.
4000
100
80
IR Spectrum
B
60
% of base peak
10
3000
40
13C NMR Spectrum
(900 MHE. COO, sution)
80
proton decoupled
9
200
'H NMR Spectrum
(200 MHz, CDC, solution)
DEPT CH CH. CH
91
2000
120
v (om¹)
160
m/e
160
группи
1600
expension
M
196/200
200
ele
1200
120
Mass Spectrum
C₂H₁1 Br
240
Resolves o
two signals
800
Resolves into
280
solvent
80
ppm
0.0
0.5
1.0
1.5
brance
200
3
Problem 91
40
h
UV spectrum
5.30 mg / 10 me
path lenge
1.00am
solvent: cyclohexane
250
2
expansions
300
λ (nm)
35.0 34.0
0
ppm
350
& (ppm)
TIMIS
O
8 (ppm)
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