Concept explainers
(a)
Interpretation:
Lewis structure of periodate ion
Concept Introduction:
Lewis structure represents covalent bonds and describes valence electrons configuration of atoms. The covalent bonds are depicted by lines and unshared electron pairs by pairs of dots. The sequence to write Lewis structure of some molecule is given as follows:
- The central atom is identified and various other atoms are arranged around it. This central atom so chosen is often the least electronegative.
- Total valence electrons are estimated for each atom.
- A single bond is first placed between each atom pair.
- The electrons left can be allocated as unshared electron pairs or as multiple bonds around
symbol of element to satisfy the octet (or duplet) for each atom. - Add charge on overall structure in case of polyatomic cation or anion.
(a)

Explanation of Solution
The molecule
The symbol for oxygen is
The symbol for iodine is
One negative charge on molecule is added up as one valence electron in total count.
Thus total valence electrons are sum of the valence electrons for each atom in
The skeleton structure in
To complete the valence electrons of iodine, it forms double bond with three oxygen atoms.
Hence, the Lewis structure for
To complete the octet of iodine atom the negative charge is delocalized on each oxygen atom and since there are four oxygen atoms, therefore, four resonance structures will be formed and possible resonance structures are as follows:
(b)
Interpretation:
Lewis structure of hydrogen phosphate ion
Concept Introduction:
Refer to part (a).
(b)

Explanation of Solution
Hydrogen phosphate ion
The symbol for oxygen is
The symbol for hydrogen is
The symbol for phosphorus is
Two negative charges on molecule are added up as one valence electron in total count.
Thus total valence electrons are sum of the valence electrons for each atom in
The skeleton structure in
To complete the valence electrons of phosphorous, it forms double bond with one oxygen atom.
Hence, 20 electrons are allocated as 10 lone pairs on remaining oxygen atoms to complete their octet. The Lewis structure is as follows:
The negative charge is delocalized on three oxygen atoms and therefore three resonance structures will be formed and possible resonance structures are as follows:
(c)
Interpretation:
Lewis structure of chloric acid
Concept Introduction:
Refer to part (a).
(c)

Explanation of Solution
Chloric acid
The symbol for oxygen is
The symbol for hydrogen is
The symbol for chlorine is
Thus total valence electrons are sum of the valence electrons for each atom in
The skeleton structure in
To complete the valence electrons of chlorine, it forms double bond with two oxygen atoms.
Hence, 14 electrons are allocated as 6 lone pairs on remaining oxygen atoms and 1 lone pair on chlorine to complete their respective octet. The Lewis structure is as follows:
The lone pair on oxygen atom that is attached to chlorine participates in resonance with that and produces
(d)
Interpretation:
Lewis structure of arsenate ion
Concept Introduction:
Refer to part (a).
(d)

Explanation of Solution
Arsenate ion
The symbol for oxygen is
The symbol for arsenic is
The symbol for chlorine is
Three negative charges on molecule is added up as three valence electrons in total count. Thus total valence electrons are sum of the valence electrons for each atom in arsenate ion
The skeleton structure in arsenate ion
To complete the valence electrons of arsenic, it forms double bond with one oxygen atom.
Hence, 22 electrons are allocated as 11 lone pairs on remaining oxygen atoms to complete their octet. The Lewis structure is as follows:
The negative charge is delocalized on each oxygen atom and since there are four oxygen atoms, therefore, four resonance structures will be formed and possible resonance structures are as,
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Chapter 2 Solutions
ACHIEVE/CHEMICAL PRINCIPLES ACCESS 2TERM
- For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects O donating O withdrawing O no inductive effects Resonance Effects Overall Electron-Density ○ donating ○ withdrawing O no resonance effects O electron-rich O electron-deficient O similar to benzene Cl O donating O withdrawing ○ donating ○ withdrawing O no inductive effects O no resonance effects O Explanation Check O electron-rich O electron-deficient similar to benzene X © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessarrow_forwardIdentifying electron-donating and For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects NH2 ○ donating NO2 Explanation Check withdrawing no inductive effects Resonance Effects Overall Electron-Density ○ donating O withdrawing O no resonance effects O donating O withdrawing O donating withdrawing O no inductive effects Ono resonance effects O electron-rich electron-deficient O similar to benzene O electron-rich O electron-deficient O similar to benzene olo 18 Ar 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibilityarrow_forwardRank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. Explanation Check Х (Choose one) OH (Choose one) OCH3 (Choose one) OH (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forward
- Assign R or S to all the chiral centers in each compound drawn below porat bg 9 Br Brarrow_forwarddescrive the energy levels of an atom and howan electron moces between themarrow_forwardRank each set of substituents using the Cahn-Ingold-Perlog sequence rules (priority) by numbering the highest priority substituent 1.arrow_forward
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning

