CHEMISTRY-TEXT
CHEMISTRY-TEXT
8th Edition
ISBN: 9780134856230
Author: Robinson
Publisher: PEARSON
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Chapter 7, Problem 7.23P

Calculate formal charges on the C and O atoms in two resonance structures for acetic acid, the main component of vinegar. Decide which structure makes a larger contribution to the resonance hybrid.
Chapter 7, Problem 7.23P, Calculate formal charges on the C and O atoms in two resonance structures for acetic acid, the main

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A resonance hybrid is a structure that can be depicted by more than one valid Lewis structure. part1: Draw the major resonance form of fulminic acid, HCNO, with the atoms connected as indicated in the formula. Your structure should have nonzero formal charges minimized, and it should include all nonzero formal charges and all nonbonding electrons. part2: Draw the second most important resonance form of fulminic acid, HCNO, with the atoms connected as indicated in the formula. Your structure should have nonzero formal charges minimized, and it should include all nonzero formal charges and all nonbonding electrons. part3: Draw the least important resonance contributor for fulminic acid, HCNO, with the atoms connected as indicated in the formula. Your structure should have nonzero formal charges minimized and should include all nonzero formal charges and all nonbonding electrons.
The carbonate anion, CO32- , is a resonance hybrid. Draw all of the important resonance structures for this molecule. If an atom has a nonzero formal charge, be sure the formal charge is shown clearly in the structure. Use the resonance structures to calculate the average formal charge on each O atom (which are all equivalent in the "true" structure). [Note: all of the important contributing resonance structures have octets around each atom that desires an octet.]
Carbon, nitrogen, and oxygen form two different polyatomic ions: cyanate ion (NCO) and fulminate ion (CNO). Write Lewis structures for each anion, including near-equivalent resonance structures (do not add any arrows between structures) and indicating formal charges. The isocyanate ion also has two near-equivalent structures, but the formal charge on the nitrogen attom cannot be reduced to zero: Cyanate ion (NCO)

Chapter 7 Solutions

CHEMISTRY-TEXT

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Use...Ch. 7 - Draw three resonance structures for sulfur...Ch. 7 - Some mothballs used when storing clothes are made...Ch. 7 - Four different structures (a), (b), (c), and (d)...Ch. 7 - Draw an electron-dot structure for carbon...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Calculate formal charges for the C and O atoms in...Ch. 7 - Draw two electron-dot resonance structures that...Ch. 7 - Draw two electron-dot resonance structures that...Ch. 7 - Prob. 7.102SPCh. 7 - Prob. 7.103SPCh. 7 - Boron trifluoride reacts with dimethyl ether to...Ch. 7 - Thiofulminic acid, HCNS, has recently been...Ch. 7 - Draw two rcsonancc strutur for methyl isocyanate,...Ch. 7 - In the cyanatc ion. OCN , carbon is the central...Ch. 7 - Prob. 7.108MPCh. 7 - Prob. 7.109MPCh. 7 - Prob. 7.110MPCh. 7 - The neutral OH molecule has been implicated in...Ch. 7 - Prob. 7.112MPCh. 7 - Prob. 7.113MP
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