4000 100 80 60 IR Spectrum (liquid film) للللللم 40 20 % of base peak 3000 40 10 13C NMR Spectrum (50.0 MHz, CDCI, solution) 80 proton decoupled 9 200 ¹H NMR Spectrum (200 MHz, CDCI, solution) DEPT CH₂ CH₂ CH expansion 4.0 101 8 120 W 2000 1736 v (cm¹) 129 m/e 160 7 1600 160 M+ 174 2.0 6 1200 120 200 240 280 ppm 800 Mass Spectrum 5 C8H1404 solvent L 80 1 4 L 1 3 No significant UV absorption above 220 nm 40 1 2 08 (ppm) 1 TMS 0 8 (ppm)
Analyzing Infrared Spectra
The electromagnetic radiation or frequency is classified into radio-waves, micro-waves, infrared, visible, ultraviolet, X-rays and gamma rays. The infrared spectra emission refers to the portion between the visible and the microwave areas of electromagnetic spectrum. This spectral area is usually divided into three parts, near infrared (14,290 – 4000 cm-1), mid infrared (4000 – 400 cm-1), and far infrared (700 – 200 cm-1), respectively. The number set is the number of the wave (cm-1).
IR Spectrum Of Cyclohexanone
It is the analysis of the structure of cyclohexaone using IR data interpretation.
IR Spectrum Of Anisole
Interpretation of anisole using IR spectrum obtained from IR analysis.
IR Spectroscopy
Infrared (IR) or vibrational spectroscopy is a method used for analyzing the particle's vibratory transformations. This is one of the very popular spectroscopic approaches employed by inorganic as well as organic laboratories because it is helpful in evaluating and distinguishing the frameworks of the molecules. The infra-red spectroscopy process or procedure is carried out using a tool called an infrared spectrometer to obtain an infrared spectral (or spectrophotometer).
![IR Spectrum
(liquid film)
4000
100
80
60
40
20
3000
40
13C NMR Spectrum
(50.0 MHz, CDCI, solution)
10
الليسا
80
proton decoupled
¹H NMR Spectrum
DEPT CH₂ CH₂ CH
200
9
(200 MHz, CDCI, solution)
101
expansion
4.0
2000
8
1736
v (cm¹)
129
1600
solvent
160
120
80
40
11
2.0
ppm
120 160 200
m/e
M+
174
7
1200
1
6
800
Mass Spectrum
C8H1404
240 280
5
4
No significant UV
absorption above 220 nm
3
2
0 8 (ppm)
1
TMS
1
0
8 (ppm)](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fe4b2eb66-6876-46cd-8986-470643caa28d%2F0fb842dd-f19c-441d-a87f-6a354f245b7a%2F5mpzbj_processed.jpeg&w=3840&q=75)
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