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...
icon
Related questions
Question
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)
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)
Expert Solution
steps

Step by step

Solved in 2 steps with 1 images

Blurred answer
Knowledge Booster
Mass Spectrometry
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
Chemistry
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
Principles of Instrumental Analysis
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
Elementary Principles of Chemical Processes, Bind…
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY