Include the 'H-NMR and 1³C-NMR data for the product in separate tables with a labeled diagram 'H: chemical shift (experimental), chemical shift (literature), multiplet structure, integration, assignment 13C: chemical shift (experimental), chemical shift (literature), assignment In the current experiment, we will use a different electrophile (the tert.-butyl cation) to alkylate 1,4-dimethoxybenzene. This is a Friedel-Crafts Alkylation reaction. OCH3 (H;C),C. OCH3 (CH3),COH CH;COOH/H,SO4 H;CO H,CO C(CH3)3 Characterization IV • 13C-NMR Spectrum • Six signals from compounds and three lines from NMR solvent 8(ppm) Assignment 29.8 C(CH;); | C(CH;); OCH3 34.6 55.9 Arene-C ortho to OCH3 Arene-C attached to C(CH;); Arene-C attached to OCH; |CDCI, (three lines) 111.7 136,3 152.0 77 -1633

EBK A SMALL SCALE APPROACH TO ORGANIC L
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Chapter30: Resolution Of (6)-a-phenylethylamine And Determination Of Optical Purity
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Electrophilic Aromatic Substitution: Friedel-Crafts Alkylation

please include experimental literature

 

Include the 'H-NMR and 1C-NMR data for the product in separate tables with a labeled
diagram
'H: chemical shift (experimental), chemical shift (literature), multiplet structure,
integration, assignment
13C: chemical shift (experimental), chemical shift (literature), assignment
In the current experiment, we will use a different electrophile (the tert.-butyl cation) to alkylate
1,4-dimethoxybenzene. This is a Friedel-Crafts Alkylation reaction.
OCH3
(H;C);C.
OCH3
(CH3);COH
CH;COOH/H,SO4
H;CO
H,CO
C(CH3);
Characterization IV
• 13C-NMR Spectrum
• Six signals from compounds and three lines from
NMR solvent
8(ppm)
Assignment
29.8
C(CH;);
C(CH;);
OCH,
34.6
55.9
Arene-C ortho to OCH;
Arene-C attached to C(CH;)3
111.7
136,3
152.0
Arene-C attached to OCH;
77
CDCI, (three lines)
-151.98
-13633
60'III-
Transcribed Image Text:Include the 'H-NMR and 1C-NMR data for the product in separate tables with a labeled diagram 'H: chemical shift (experimental), chemical shift (literature), multiplet structure, integration, assignment 13C: chemical shift (experimental), chemical shift (literature), assignment In the current experiment, we will use a different electrophile (the tert.-butyl cation) to alkylate 1,4-dimethoxybenzene. This is a Friedel-Crafts Alkylation reaction. OCH3 (H;C);C. OCH3 (CH3);COH CH;COOH/H,SO4 H;CO H,CO C(CH3); Characterization IV • 13C-NMR Spectrum • Six signals from compounds and three lines from NMR solvent 8(ppm) Assignment 29.8 C(CH;); C(CH;); OCH, 34.6 55.9 Arene-C ortho to OCH; Arene-C attached to C(CH;)3 111.7 136,3 152.0 Arene-C attached to OCH; 77 CDCI, (three lines) -151.98 -13633 60'III-
Characterization II
• 'H-NMR Spectrum
• Three signals from compound and one from
NMR solvent
8(ppm) Multiplet Int Assignment
18 | С(CH)
6 ОСН,
1.4
S
3
3.6
S
6.7
S
2 Arene-H
7.3
CHCI; in CDCI3
S
NMR spectra (CDC13): 'H-NMR: 400 MHz, 1³C-NMR: 100 MHz
10.5
10.0
9.5
9.0
8.5
8.0
7.5
7.0
6.5
6.0
5.5
5.0
fi (ppm)
0.5
4.5
4.0
3.5
3.0
2.5
2.0
1.5
1.0
0.0
-0.5
-1.0
Transcribed Image Text:Characterization II • 'H-NMR Spectrum • Three signals from compound and one from NMR solvent 8(ppm) Multiplet Int Assignment 18 | С(CH) 6 ОСН, 1.4 S 3 3.6 S 6.7 S 2 Arene-H 7.3 CHCI; in CDCI3 S NMR spectra (CDC13): 'H-NMR: 400 MHz, 1³C-NMR: 100 MHz 10.5 10.0 9.5 9.0 8.5 8.0 7.5 7.0 6.5 6.0 5.5 5.0 fi (ppm) 0.5 4.5 4.0 3.5 3.0 2.5 2.0 1.5 1.0 0.0 -0.5 -1.0
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