Consider the formate ion, HCO2, which is the anion formed when formic acid loses an H* ion. The H and the two O atoms are bonded to the central C atom. (a) Draw the best Lewis structure(s) for this ion. (b) Are resonance structures needed to describe the structure? Explain briefly (c) Would you predict that the C-0 bond lengths in the formate ion would be longer or shorter relative to those in CO2? Explain briefly

Chemistry: Principles and Practice
3rd Edition
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Chapter9: Chemical Bonds
Section: Chapter Questions
Problem 9.72QE: Write all resonance structures of chlorobenzene, C6H5Cl, a molecule with the same cyclic structure...
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Consider the formate ion, HCO2", which is the anion
formed when formic acid loses an H* ion. The H and
the two O atoms are bonded to the central C atom.
(a) Draw the best Lewis structure(s) for this ion.
(b) Are resonance structures needed to describe the
structure? Explain briefly
(c) Would you predict that the C-O bond lengths in
the formate ion would be longer or shorter relative to
those in CO2? Explain briefly
Transcribed Image Text:Consider the formate ion, HCO2", which is the anion formed when formic acid loses an H* ion. The H and the two O atoms are bonded to the central C atom. (a) Draw the best Lewis structure(s) for this ion. (b) Are resonance structures needed to describe the structure? Explain briefly (c) Would you predict that the C-O bond lengths in the formate ion would be longer or shorter relative to those in CO2? Explain briefly
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