Pushing Electrons
4th Edition
ISBN: 9781133951889
Author: Weeks, Daniel P.
Publisher: Cengage Learning
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Chapter 3, Problem 8EQ
Interpretation Introduction
Interpretation:
The leaving group in the given molecule is to be determined in order identify the positively charged and neutral fragments produced during mechanism.
Concept Introduction:
Heterolytic cleavage of sigma bond occurs under a variety of conditions. The mechanism of bond cleavage is as shown below,
The arrow in the above mechanism indicates that the sigma electrons form A-B bond are leaving A and becoming the exclusive property of B. Since the fragment A is formally losing one electron, it must become positively charged and B must become negatively charged since it gains an electron.
Often, heterolytic cleavage occurs from a charged intermediate that was formed in a previous step. The process is the same, but the charge on the products is different.
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Many free radicals combine to form molecules that do not contain any unpaired electrons. The driving force for the radical-
radical combination reaction is the formation of a new electron-pair bond.
Consider the formation of hydrogen peroxide.
2 OH(g) → H₂O₂(g)
Write Lewis formulas for the reactant and product species in the chemical equation. Include nonbonding electrons.
OH(g)
Select Draw Rings More
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H₂O₂(g)
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Question Source: McQuarrie, Rock, And Gallogly 4e - General Chemistry
Publisher: University Science B
I had gotten this one incorrect, but i wanted to use it to study, so please give me the solution to all parts of this question.
Many free radicals combine to form molecules that do not contain any unpaired electrons. The driving force for the radical-radical combination reaction is the formation of a new electron-pair bond. Consider the chemical equation. N(g)+NO(g) NNO(g) Write Lewis formulas for the reactant and product species in the chemical equation. Include nonbonding electrons.
Chapter 3 Solutions
Pushing Electrons
Ch. 3 - Prob. 1EQCh. 3 - Prob. 2EQCh. 3 - Prob. 3EQCh. 3 - Prob. 4EQCh. 3 - Prob. 5EQCh. 3 - Prob. 6EQCh. 3 - Here are some exercises in sigma bond breaking....Ch. 3 - Prob. 8EQCh. 3 - Prob. 9EQCh. 3 - Prob. 10EQ
Ch. 3 - Prob. 11EQCh. 3 - Prob. 12EQCh. 3 - Prob. 13EQCh. 3 - Prob. 14EQCh. 3 - Prob. 15EQCh. 3 - Prob. 16EQCh. 3 - Prob. 17EQCh. 3 - Prob. 18EQCh. 3 - Prob. 19EQCh. 3 - Prob. 20EQCh. 3 - Prob. 21EQCh. 3 - Prob. 22EQCh. 3 - Prob. 23EQCh. 3 - Prob. 24EQCh. 3 - Prob. 25EQCh. 3 - Prob. 26EQCh. 3 - Prob. 27EQCh. 3 - Prob. 28EQCh. 3 - Prob. 29EQCh. 3 - Prob. 30EQCh. 3 - The reaction just described is reversible....Ch. 3 - Prob. 32EQCh. 3 - Prob. 59EQ
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