LM 3410 4000 100 40 3000 80 "C NMR Spectrum (500 MHz, CDC, solution) ORGANIC STRUCTURES FROM SPECTRA IR Spectrum qu 2000 1600 V (cm) M-86 (15) 120 160 200 m/e 1200 800 Mass Spectrum 240 C₂H₂O 280 115 No significant UV absorption above 220 m IR: List bands and possible/probable structural units responsible Band (cm³) Possible stretches/functional groups MS: Molecular Formula 13C NMR: 1 2 3 4 Chem. Shift (8) Type of C (sp, sp², carbonyl, etc.) IHD(DU) = (Show calculation) # of attached H's # of identical C's in signal
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).
![4000
100
80
60
40
20
3410
tele
3000
40
10
43
¹3C NMR Spectrum
(50.0 MHz, CDCI, solution)
proton decoupled
6.0
DEPT CH, CH₂ 1 CH 1
9
71
80
200
¹H NMR Spectrum
(200 MHz, CDCI, solution)
expansion
ORGANIC STRUCTURES FROM SPECTRA
5.5
8
IR Spectrum
(liquid film)
2000
M 86 (1%)
120
V (cm)
m/e
160
1600
7
160 200
5.0 ppm
6
120
1200
J
Mass Spectrum
240
800
5
CsH10O
280
solvent
80
4
exchanges
with D.O
1
L
3
40
No significant UV
absorption above 220 nm
2
E Q
115
08 (ppm)
1
TMS
L
0
ō (ppm)
IR: List bands and possible/probable structural units responsible
Band (cm³)
Possible stretches/functional groups
MS:
Molecular Formula,
13C NMR:
1
2
3
4
5
6
Chem. Shift (8) Type of C (sp), sp²,
carbonyl, etc.)
¹H NMR:
1
Chem. Shift (8) Multiplicity (singlet,
doublet, etc.)
IHD(DU)=
2
3
4
5
6
If you need more space, add any additional signal info here:
(Show calculation)
# of attached H's
# of identical C's in
signal
Probable Type of H
(methyl, aromatic, etc.)
# of identical H's
in signal](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fd5015106-388e-4d6b-8592-fff9867f652a%2F75c49dc1-af66-477d-8dd4-573fc688ce99%2F4q5zkjm_processed.jpeg&w=3840&q=75)
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