:Br: + :Ö-

Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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What are the product(s) of the reaction and the lone pairs, if any?

The image depicts a chemical reaction involving two compounds. On the left side, there's a structure representing an organic compound with a bromine (Br) atom attached. The bromine is shown with three lone pairs of electrons. The aliphatic chain connected to bromine suggests an alkyl bromide structure.

Next to it, a plus sign indicates a reaction with another molecule. On the right side, there's a structure showing an ethoxide ion. This ion has an oxygen atom with a negative charge, represented by a minus sign, and two lone pairs of electrons. The oxygen is connected to an ethyl group.

This depicts a typical substitution reaction where the ethoxide ion (a nucleophile) would likely attack the carbon atom bonded to bromine, replacing the bromine atom and forming a new compound. This is a common step in organic synthesis, often leading to an ether product through a bimolecular nucleophilic substitution (S<sub>N</sub>2) mechanism.
Transcribed Image Text:The image depicts a chemical reaction involving two compounds. On the left side, there's a structure representing an organic compound with a bromine (Br) atom attached. The bromine is shown with three lone pairs of electrons. The aliphatic chain connected to bromine suggests an alkyl bromide structure. Next to it, a plus sign indicates a reaction with another molecule. On the right side, there's a structure showing an ethoxide ion. This ion has an oxygen atom with a negative charge, represented by a minus sign, and two lone pairs of electrons. The oxygen is connected to an ethyl group. This depicts a typical substitution reaction where the ethoxide ion (a nucleophile) would likely attack the carbon atom bonded to bromine, replacing the bromine atom and forming a new compound. This is a common step in organic synthesis, often leading to an ether product through a bimolecular nucleophilic substitution (S<sub>N</sub>2) mechanism.
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