ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5
ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5
2nd Edition
ISBN: 9780393664034
Author: KARTY
Publisher: NORTON
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Chapter 12, Problem 12.34P
Interpretation Introduction

Interpretation:

Br2 undergoes electrophilic addition to maleic anhydride as shown in the given reaction. The reason for this reaction being slower than the analogous one with cyclopentene is to be explained.

Concept introduction:

Molecular bromine undergoes anti addition across a C=C double bond. As the electron-rich alkene approaches Br2 molecule, it temporarily generates an electron-poor site on the Br atom closer to the alkene. The subsequent flow of electrons takes place between the electron-rich alkene and the electron-poor Br atom. The presence of an electron withdrawing group near to the C=C double bond makes it less electron rich which can diminish the driving force for the electrophilic addition step.

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Can you help me figure out the full mechanism of this reaction?
Please complete the mechanism of the following reaction.
a. Explain why the alkyl halide shown here reacts much more rapidly with guanine than does a primary alkyl halide (such as pentyl chloride). b. The alkyl halide can react with two guanines, each in a different DNA chain, thereby cross-linking the chains. Propose a mechanism for thecross- linking reaction.

Chapter 12 Solutions

ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5

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