1 Transmittance (%) 60 40 20 0 A- FTIR spectrum 4000 3500 5.10 5.0 5.05 3000 4.5 ppm 2500 4.0 2000 Wavenumber (cm-¹) B: ¹H NMR spectrum (300 MHz) 8 1.59 (3H, d, J=1.4 Hz) 1.67 (3H, d, J=1.4 Hz), 2.09 (3H, s), 2.24 (2H, q, J=7.2 Hz), 2.41 (2H, t, J=7.2Hz), 5.05 (1H 3 x 7 lines, J=7.2, 1.4Hz) 1718 3.5 2.4 2.3 3.0 Figure 5 ppm проти 2.5 1500 2.0 1000 1.7 1.5 1.6 ppm 500 ppm
1 Transmittance (%) 60 40 20 0 A- FTIR spectrum 4000 3500 5.10 5.0 5.05 3000 4.5 ppm 2500 4.0 2000 Wavenumber (cm-¹) B: ¹H NMR spectrum (300 MHz) 8 1.59 (3H, d, J=1.4 Hz) 1.67 (3H, d, J=1.4 Hz), 2.09 (3H, s), 2.24 (2H, q, J=7.2 Hz), 2.41 (2H, t, J=7.2Hz), 5.05 (1H 3 x 7 lines, J=7.2, 1.4Hz) 1718 3.5 2.4 2.3 3.0 Figure 5 ppm проти 2.5 1500 2.0 1000 1.7 1.5 1.6 ppm 500 ppm
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter5: Resonance
Section: Chapter Questions
Problem 2CTQ: You will not find “hydroxide” in the stockroom, but you will find sodium hydroxide (NaOH)...
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Answer and explain in detail how you arrived at that answer.

Transcribed Image Text:1
Transmittance (%)
60
40
20
0
A- FTIR spectrum
4000
3500
5.10
5.0
5.05
3000
4.5
ppm
2500
2000
Wavenumber (cm-¹)
B: ¹H NMR spectrum (300 MHz)
8 1.59 (3H, d, J=1.4 Hz) 1.67 (3H, d, J=1.4 Hz), 2.09 (3H, s), 2.24 (2H, q, J=7.2 Hz),
2.41 (2H, t, J-7.2Hz), 5.05 (1H 3 x 7 lines, J=7.2, 1.4Hz)
4.0
1718
3.5
JALL
2.4
2.3
1.7
ppm
3.0
1500
Figure 5
проти
2.5
1000
2.0
1.5
1.6
ppm
500
ppm

Transcribed Image Text:11. Spectra of an organic compound X are shown in Figure (A and B). Predict the
chemical structure of compound X with molecular formula C8H₁4O.
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