Organic Chemistry Study Guide and Solutions
6th Edition
ISBN: 9781936221868
Author: Marc Loudon, Jim Parise
Publisher: W. H. Freeman
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Question
Chapter 1, Problem 1.32AP
Interpretation Introduction
(a)
Interpretation:
The negative charge present on each oxygen atom of the carbonate ion is to be calculated.
Concept introduction:
Resonance structure is a blend of two or more Lewis structures. Resonance structures are represented by a double headed arrow between the structures. Three resonance structrues are possible for carbonate ion.
Interpretation Introduction
(b)
Interpretation:
The bond order of each carbon-oxygen bond in the carbonate ion is to be calculated.
Concept introduction:
Resonance structure is a blend of two or more Lewis structures. Resonance structures are represented by a double headed arrow between the structures. Three resonance structures are possible for carbonate ion.
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3)
The molecule diphosphorus tetraoxide (P,O,) has two central atoms and four different resonance
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shorter than the O-O bond in O2? Explain.
8.37 Which of the following statements about electronegativity is
false? (a) Electronegativity is the ability of an atom in a molecule
to attract electron density toward itself. (b) Electronegativity is
the same thing as electron affinity. (c) The numerical values
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element.
8,38 (a) What is the trend in electronegativity going from
Some chemists believe that satisfaction of the octet rule should be the top criterion
for choosing the dominant Lewis structure of a molecule or ion. Other chemists
believe that achieving the best formal charges should be the top criterion.
Consider the dihydrogen phosphate ion, HaPO, , in which the H atoms are bonded
to O atoms. (a) What is the predicted dominant Lewis structure if satisfying the
octet rule is the top eriterion? (b) What is the predicted dominant Lewis structure if
achieving the best formal charges is the top criterion?
Chapter 1 Solutions
Organic Chemistry Study Guide and Solutions
Ch. 1 - Prob. 1.1PCh. 1 - Prob. 1.2PCh. 1 - Prob. 1.3PCh. 1 - Prob. 1.4PCh. 1 - Prob. 1.5PCh. 1 - Prob. 1.6PCh. 1 - Prob. 1.7PCh. 1 - Prob. 1.8PCh. 1 - Prob. 1.9PCh. 1 - Prob. 1.10P
Ch. 1 - Prob. 1.11PCh. 1 - Prob. 1.12PCh. 1 - Prob. 1.13PCh. 1 - Prob. 1.14PCh. 1 - Prob. 1.15PCh. 1 - Prob. 1.16PCh. 1 - Prob. 1.17PCh. 1 - Prob. 1.18PCh. 1 - Prob. 1.19PCh. 1 - Prob. 1.20PCh. 1 - Prob. 1.21APCh. 1 - Prob. 1.22APCh. 1 - Prob. 1.23APCh. 1 - Prob. 1.24APCh. 1 - Prob. 1.25APCh. 1 - Prob. 1.26APCh. 1 - Prob. 1.27APCh. 1 - Prob. 1.28APCh. 1 - Prob. 1.29APCh. 1 - Prob. 1.30APCh. 1 - Prob. 1.31APCh. 1 - Prob. 1.32APCh. 1 - Prob. 1.33APCh. 1 - Prob. 1.34APCh. 1 - Prob. 1.35APCh. 1 - Prob. 1.36APCh. 1 - Prob. 1.37APCh. 1 - Prob. 1.38APCh. 1 - Prob. 1.39APCh. 1 - Prob. 1.40APCh. 1 - Prob. 1.41APCh. 1 - Prob. 1.42APCh. 1 - Prob. 1.43APCh. 1 - Prob. 1.44APCh. 1 - Prob. 1.45APCh. 1 - Prob. 1.46APCh. 1 - Prob. 1.47APCh. 1 - Prob. 1.48APCh. 1 - Prob. 1.49AP
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