Due to time constraints, the preparation of 1-iodo-4-nitrobenzene was no longer included in today's experiment. However, if it was, you would have used IR to confirm you synthesized 1-iodo-4- nitrobenzene from p-nitroaniline. How can IR spectroscopy differentiate these two compounds? To assist with answering this question, see the IR spectra of these compounds in Fig. 1-2. 4800 LOD D 4000 3000 3000 BOOK 1500 AVENUE Figure 1. IR spectrum of 1-iodo-4-nitrobenzene exce VEMBER Figure 2. IR spectrum of p-nitroaniline 1000 M 1000

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3.
Due to time constraints, the preparation of 1-iodo-4-nitrobenzene was no longer included in today's
experiment. However, if it was, you would have used IR to confirm you synthesized 1-iodo-4-
nitrobenzene from p-nitroaniline. How can IR spectroscopy differentiate these two compounds? To assist
with answering this question, see the IR spectra of these compounds in Fig. 1-2.
100
D
4800
LOD
|FARONI || RAGIS!
D
4800
3000
3000
BOO
AVENUMBER
2000
Figure 1. IR spectrum of 1-iodo-4-nitrobenzene
1500
HAVENUMBRI
4500
Figure 2. IR spectrum of p-nitroaniline
1000
1000
500
500
Transcribed Image Text:3. Due to time constraints, the preparation of 1-iodo-4-nitrobenzene was no longer included in today's experiment. However, if it was, you would have used IR to confirm you synthesized 1-iodo-4- nitrobenzene from p-nitroaniline. How can IR spectroscopy differentiate these two compounds? To assist with answering this question, see the IR spectra of these compounds in Fig. 1-2. 100 D 4800 LOD |FARONI || RAGIS! D 4800 3000 3000 BOO AVENUMBER 2000 Figure 1. IR spectrum of 1-iodo-4-nitrobenzene 1500 HAVENUMBRI 4500 Figure 2. IR spectrum of p-nitroaniline 1000 1000 500 500
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