Analyze the H1 NMR of methyl trans-cinnamte prepared via Fischer esterification, and write its  Observed Shift, Observed Splitting and observed Integration for all peaks?

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution
Section16.4: Substituent Effects In Electrophilic Substitutions
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Analyze the H1 NMR of methyl trans-cinnamte prepared via Fischer esterification, and write its 

Observed Shift, Observed Splitting and observed Integration for all peaks?

E22A.1 PREPARATION OF METHYL trans-CINNAMATE:
A COMPONENT OF STRAWBERRY AROMA
O
H
CC=C
OH
H2SO4
H
+ CH3OH
A
trans-cinnamic acid
methanol
H
C=C
OCH3
H
+ H₂O
methyl trans-cinnamate
Transcribed Image Text:E22A.1 PREPARATION OF METHYL trans-CINNAMATE: A COMPONENT OF STRAWBERRY AROMA O H CC=C OH H2SO4 H + CH3OH A trans-cinnamic acid methanol H C=C OCH3 H + H₂O methyl trans-cinnamate
FI: 60.201
EX: c:\eft\HI\ACQ.ppg
8
7
IC
H NMR of Product
methyl trans-cinnamate
7.839
7.555
7.505
7.421
7.402
7.351
7.290
6.553
6.285
5.998
3.790
on
CH 3
6
5
4
3
2
1
0
PPM
USER:
--
DATE: 03/21/24 (15:55)
SWI: 3994
PW: 2.4 us
PD: 3.5 sec
OF1: 361.3
NA: 5
PTS1d: 4096
LB: 0.0
0.161
-0.000
Transcribed Image Text:FI: 60.201 EX: c:\eft\HI\ACQ.ppg 8 7 IC H NMR of Product methyl trans-cinnamate 7.839 7.555 7.505 7.421 7.402 7.351 7.290 6.553 6.285 5.998 3.790 on CH 3 6 5 4 3 2 1 0 PPM USER: -- DATE: 03/21/24 (15:55) SWI: 3994 PW: 2.4 us PD: 3.5 sec OF1: 361.3 NA: 5 PTS1d: 4096 LB: 0.0 0.161 -0.000
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