
Concept explainers
(a)
Interpretation:
The electron geometries of all nonhydrogen atoms in the four listed species are to be determined.
Concept introduction:
Electron geometry around an atom is determined on the basis of the Valence Shell Electron Pair Repulsion (VSEPR) Theory. Electron geometry describes the orientation of the electron groups in an atom’s valence shell. An electron group is a lone pair or a bond between the two atoms. The bond, whether a single, double or triple, counts as just one electron group.
Since all electrons have the same charge, the electron groups repel each other. They try to move (orient themselves) as far away from each other as possible in order to minimize these repulsions. This results in a linear geometry (
The number of electron groups and geometry is determined on the basis of the Lewis structure of the molecule/ion.
(b)
Interpretation:
The hybridization of all nonhydrogen atoms in the given four species is to be determined.
Concept introduction:
The concept of hybridization of atomic orbitals is used in Valence Bond (VB) Theory to account for the electron and molecular geometry around an atom. A hybrid orbital is a combination of one or more atomic orbitals from the valence shell of an atom. It typically involves an s orbital and a number of p orbitals from the valence shell, resulting in the same total number of hybrid orbitals of the same energy and shape. In heavy atoms, those from Group 3 onward, the valence shell d orbital may also be involved if the atom has an expanded octet. The orientation of these orbitals is same as the electron geometry of the atom. The number of hybrid orbitals required is the same as the number of electron groups. If the number of electron groups is two, two hybrid orbitals are needed. These are formed by a combination of the s and one p orbital, giving

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Chapter 3 Solutions
EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
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- → Acetyl-CoA + 3NAD+ + 1FAD + 1ADP 2CO2 + CoA + 3NADH + 1FADH2 + 1ATP a. Which of the above are the reactants? b. Which of the above are the products? c. Which reactant is the electron donor? d. Which reactants are the electron acceptors? e. Which of the products are now reduced? f. Which product is now oxidized? g. Which process was used to produce the ATP? h. Where was the energy initially in this chemical reaction and where is it now that it is finished? i. Where was the carbon initially in this chemical reaction and where is it now that it is finished? j. Where were the electrons initially in this chemical reaction and where is it now that it is finished?arrow_forwardRank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. OCH 3 (Choose one) OH (Choose one) Br (Choose one) Explanation Check NO2 (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Aarrow_forwardFor 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_forward
- Identifying 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_forwardAssign R or S to all the chiral centers in each compound drawn below porat bg 9 Br Brarrow_forward
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning

