Provide a structure for the compound with the formula C, H,, NO using the given information. 13 IR: 3360, 3280 cm- (doublet); 1611 cm-; no carbonyl absorption; 'H NMR spectrum: chemical shift, Hz 1200 2400 2100 1800 1500 900 600 300 3H J = 6.9 Hz J = 6.9 Hz J = 8.7 Hz J = 8.7 Hz 2H 2H 4H 2H 1 4 chemical shift, ppm (8) 8. 7 6. Draw the structure C,H3NO.

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Chapter1: Chemical Foundations
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Provide a structure for the compound with the formula C, H,NO using the given information.
13
IR: 3360, 3280 cm-
(doublet); 1611 cm-; no carbonyl absorption;
'H NMR spectrum:
chemical shift, Hz
1200
2400
2100
1800
1500
900
600
300
3H
J = 6.9 Hz
J = 6.9 Hz
J = 8.7 Hz
|= 8.7 Hz
4H
2H
2H
2H
7
4
chemical shift, ppm (8)
3
1
0.
Draw the structure C, HNO.
13
Select
Draw
Rings
More
Erase
//
C
H N
5.
6
8
Transcribed Image Text:of 10 <> Provide a structure for the compound with the formula C, H,NO using the given information. 13 IR: 3360, 3280 cm- (doublet); 1611 cm-; no carbonyl absorption; 'H NMR spectrum: chemical shift, Hz 1200 2400 2100 1800 1500 900 600 300 3H J = 6.9 Hz J = 6.9 Hz J = 8.7 Hz |= 8.7 Hz 4H 2H 2H 2H 7 4 chemical shift, ppm (8) 3 1 0. Draw the structure C, HNO. 13 Select Draw Rings More Erase // C H N 5. 6 8
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