CAREY: ORGANIC CHEMISTRY
CAREY: ORGANIC CHEMISTRY
10th Edition
ISBN: 9781260364002
Author: VALUE EDITION
Publisher: MCG CUSTOM
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Chapter 10, Problem 22P
Interpretation Introduction

Interpretation:

The compounds that are likely to be formed on free-radical addition of HBr to cis-2-pentene are to be determined and the stereochemically accurate formula for each of them is to be written, and the configuration at each chirality center is to be specified.

Concept introduction:

The number of stereoisomers formed can be calculated using the formula 2n, where n is the number of chiral centers present in the molecule.

The absolute configuration of the chiral center is determined on the basis of the following rules:

First priority of the four groups present on the carbon atoms is decided. Higher is the atomic number of the group, higher is its priority.

The compound undergoes rotation in order to get the least priority group above or below the plane.

If the least priority group is present below the plane, then clockwise arrangement of first three priority groups gives R configuration and anticlockwise gives S. Reverse is true if the least priority group is present above the plane.

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H R Part: 1/2 :CI: is a/an electrophile Part 2 of 2 Draw the skeletal structure of the product(s) for the Lewis acid-base reaction. Include lone pairs and formal charges (if applicable) on the structures. 4-7: H ö- H Skip Part Check X :C1: $ % L Fi Click and drag to start drawing a structure. MacBook Pro & ㅁ x G 0: P Add or increase positive formal cha Save For Later Submit ©2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Cente
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