11. The mass spectrum of anisole exhibits prominent peaks at mle= 108 (M* base peak), 93, 78, 77 and 65. Explain the formation of ions corresponding to these peaks. 01 (100%) 65 and metastable 00
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).
![(b) CH3-CH–CH2–Č–0–CH3 and CH3-CH2-CH,–C–OC2H5
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Mass Spectroscopy
CH3
193
Can
CH3
-CH3 and C6H5–CH2–CH–CH3.
on
of
he
(a) CgH;-C
CH3
1
CH3
3
4
a C¢H5-C-CH2-CH3 and C6H5–CH2 C–CH2
CH3
CH —CH—CHз and CH3- с сН,—СН —СН3
(d) CH3
CH3
8
7
o The mass spectrum of an alcohol C5H120 is given below (Fig. 4.12).
100
45
80-
60-
40-
20-
59
73
de
88
20
30
40
50
60
70
80
90
m/e
Fig. 4.12
Deduce the structure of the alcohol.
11. The mass spectrum of anisole exhibits prominent peaks at mle=108 (M* base peak), 93, 78,
77 and 65. Explain the formation of ions corresponding to these peaks.
12. Rationalise the formation of peaks at mle = 122 (M*), 92, 91 (100%), 65 and metastable
peaks at mle = 46.4 and 69.4 in the mass spectrum of 2-phenyl ethanol.
13. In the mass spectrum of an unknown hydrocarbon, the relative intensity of M† is 70, M† + 1
peak is 4.7 and base peak is 100. Calculate the number of carbons in the hydrocarbon.
14. Give the structure of a compound (A) C10H120 whose mass spectrum shows mle values of
15, 43, 57, 91, 105 and 148.
Fig. 4.13 and Fig. 4.14 show the mass spectra of nonane and 3, 3-dimethyl heptane. Both
iese compounds are isomeric compounds. Assign each given spectrum to the appropriate
Compound by analysing fraginentation patterns with the aid of fragmentation ions.
0. Explain the appearance of mle = 44 in the mass spectrum of butanal.
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nd Their S
Orgun-
194
100
90
Mass SpectrosCi
19. Mass spec
compound
20
(M*)
10
80
90
100
110
120
60
70
130
40
50
m/z
140
30
20
Fig. 4.13
100 r
6-8
re the peaks at mle = 113,90
- 91 and at mle = 65. Calculat.
Fehling solution and Tolleme
nd 29 are observed in its mass
pund.
at mle = 70, 55, 41, 39, 29 and
е рeaks.
--methylcyclohexene by mas
eaks at mle = 98, 83, 70, 55 and
se peaks.
Linent peaks at mle = 148 (M'),
the ions corresponding to these
% Relative Abundance
2-pentanone and 3-pentanone
ds be differentiated by mas
Relative Intensity, %](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F1aef023e-1001-4b1b-afaf-51d198cc2d25%2F635416ee-aced-40c5-94e9-24e2875937bd%2Ft0q5yz_processed.jpeg&w=3840&q=75)
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