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Ch.1 - Chemical Tools: Experimentation & Measurement

Ch.2 - Atoms, Molecules & Ions

Ch.3 - Mass Relationships in Chemical Reactions

BONUS: Lab Techniques and Procedures

BONUS: Mathematical Operations and Functions

Ch.4 - Reactions in Aqueous Solution

Ch.5 - Periodicity & Electronic Structure of Atoms

Ch.6 - Ionic Compounds: Periodic Trends and Bonding Theory

Ch.7 - Covalent Bonding and Electron-Dot Structures

Ch.8 - Covalent Compounds: Bonding Theories and Molecular Structure

Ch.9 - Thermochemistry: Chemical Energy

Ch.10 - Gases: Their Properties & Behavior

Ch.11 - Liquids & Phase Changes

Ch.12 - Solids and Solid-State Materials

Ch.13 - Solutions & Their Properties

Ch.14 - Chemical Kinetics

Ch.15 - Chemical Equilibrium

Ch.16 - Aqueous Equilibria: Acids & Bases

Ch.17 - Applications of Aqueous Equilibria

Ch.18 - Thermodynamics: Entropy, Free Energy & Equilibrium

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Ch.21 - Transition Elements and Coordination Chemistry

Ch.22 - The Main Group Elements

Ch.23 - Organic and Biological Chemistry

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Chapter 8, Problem 115a

Cyclooctatetraene dianion, C₈H₈^2-, is an organic ion with the structure shown. Considering only the p bonds and not the s bonds, cyclooctatetraene dianion can be described by the following energy diagrams of its p molecular orbitals:
<IMAGE>
(a) What is the hybridization of the 8 carbon atoms?

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Chapter 8, Problem 115a

Cyclooctatetraene dianion, C8H82-, is an organic ion with the structure shown. Considering only the p bonds and not the s bonds, cyclooctatetraene dianion can be described by the following energy diagrams of its p molecular orbitals:<IMAGE>(a) What is the hybridization of the 8 carbon atoms?

Cyclooctatetraene dianion, C₈H₈^2-, is an organic ion with the structure shown. Considering only the p bonds and not the s bonds, cyclooctatetraene dianion can be described by the following energy diagrams of its p molecular orbitals:
<IMAGE>
(a) What is the hybridization of the 8 carbon atoms?