ORG CHEM W/ EBOOK & SW5 + STUDY GUIDE
ORG CHEM W/ EBOOK & SW5 + STUDY GUIDE
2nd Edition
ISBN: 9780393666144
Author: KARTY
Publisher: NORTON
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Chapter 22, Problem 22.48P
Interpretation Introduction

Interpretation:

When anthracene is treated with Br2 in CCl4, why the addition of Br2 takes place is to be explained.

Concept introduction:

The π system of aromatic compound is relatively electron rich, in contrast, an electrophile is relatively electron poor, hence aromatic compound may undergo electrophilic addition reaction. But when benzene is treated with Cl2 or HCl, no reaction occurs. Electrophilic addition reactions that permanently destroy benzene’s aromaticity are heavily disfavored. The electrophilic addition reaction in that does not destroy the aromaticity of an aromatic compound are favored.

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1. Calculate the accurate monoisotopic mass (using all 1H, 12C, 14N, 160 and 35CI) for your product using the table in your lab manual. Don't include the Cl, since you should only have [M+H]*. Compare this to the value you see on the LC-MS printout. How much different are they? 2. There are four isotopic peaks for the [M+H]* ion at m/z 240, 241, 242 and 243. For one point of extra credit, explain what each of these is and why they are present. 3. There is a fragment ion at m/z 184. For one point of extra credit, identify this fragment and confirm by calculating the accurate monoisotopic mass. 4. The UV spectrum is also at the bottom of your printout. For one point of extra credit, look up the UV spectrum of bupropion on Google Images and compare to your spectrum. Do they match? Cite your source. 5. For most of you, there will be a second chromatographic peak whose m/z is 74 (to a round number). For one point of extra credit, see if you can identify this molecule as well and confirm by…
Please draw, not just describe!
can you draw each step on a piece of a paper please this is very confusing to me

Chapter 22 Solutions

ORG CHEM W/ EBOOK & SW5 + STUDY GUIDE

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