This synthesis was designed using the Organic Chemistry Road Map found in the appendix of your textbook compound a compound b compound c compound f W compound e NaOH compound d
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).
![This synthesis was designed using the Organic Chemistry Road Map found in the appendix of your textbook.
compound a
compound b
compound c
Reagents
HX
a.
b. HBr, H₂O₂, hv
c. H₂O, H₂SO4
d. X₂
H₂, Pd
X₂, H₂O
g. OsO4 then NaHSO3
h.
i. BH3 then H₂O₂, NaOH
e.
f.
In this synthesis, reagents from the table are used to carry out the indicated steps (shown in blue).
j.
k.
I.
compound f
O3 then (CH3)2S
2 equivalents of NaNH2
H₂, Lindlar's catalyst
compound e
Hg(OAc)2, H₂O then NaBH4
W
compound d
NaOH
m.
Na/NH3
n. H₂SO4, HgSO4
o.
p.
q.
r.
S.
t.
u.
PBr3
SOCI₂
V.
H3PO4
W. H₂CRO4
X.
PCC
104
(sia)₂BH then H₂O₂, NaOH
y.
1 equivalent of NaNH₂
NBS, hv
X2, hv
(CH3)3COK*
In the box below, draw the structure of compound f.
• Use the wedge/hash bond tools to indicate stereochemistry where it exists.
• If the reaction produces a racemic mixture, draw both stereoisomers.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F51ec3082-9306-4240-b8d9-8cb10d06f445%2F060256f2-ea2a-4c83-8e75-a8c52dc731f7%2F7qu9qfh_processed.jpeg&w=3840&q=75)
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