- Chapter 1: Chemistry: The Study of Change
- Chapter 10: Chemical Bonding II Molecular Geometry and Hybridization of Atomic Orbitals
- Chapter 11: Intermolecular Forces and Liquids and Solids
- Chapter 12: Physical Properties of Solutions
- Chapter 13: Chemical Kinetics
- Chapter 14: Chemical Equilibrium
- Chapter 15: Acids and Bases
- Chapter 16: Acid-Base Equilibria and Solubility Equilibria
- Chapter 17: Entropy, Free Energy, and Equilibrium
- Chapter 18: Electrochemistry
- Chapter 19: Nuclear Chemistry
- Chapter 2: Atoms, Molecules, and Ions
- Chapter 20: Chemistry in the Atmosphere
- Chapter 21: Metallurgy and the Chemistry of Metals
- Chapter 22: Nonmetallic Elements and Their Compounds
- Chapter 23: Transition Metals Chemistry and Coordination Compounds
- Chapter 24: Organic Chemistry
- Chapter 25: Synthetic and Natural Organic Polymers
- Chapter 3: Mass Relationships in Chemical Reactions
- Chapter 4: Reactions in Aqueous Solutions
- Chapter 5: Gases
- Chapter 6: Thermochemistry
- Chapter 7: Quantum Theory and the Electronic Structure of Atoms
- Chapter 8: Periodic Relationships Among the Elements
- Chapter 9: Chemical Bonding I Basic Concepts
Chemistry 12th Edition - Solutions by Chapter
Full solutions for Chemistry | 12th Edition
ISBN: 9780078021510
Solutions by Chapter
The full step-by-step solution to problem in Chemistry were answered by , our top Chemistry solution expert on 09/09/17, 04:35AM. Chemistry was written by and is associated to the ISBN: 9780078021510. This textbook survival guide was created for the textbook: Chemistry, edition: 12. Since problems from 25 chapters in Chemistry have been answered, more than 37315 students have viewed full step-by-step answer. This expansive textbook survival guide covers the following chapters: 25.
Key Chemistry Terms and definitions covered in this textbook
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Acylation
The process of introducing an acyl group, RCO! or ArCO!, onto an organic molecule.
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Aromatic compound
A term used initially to classify benzene and its derivatives. More accurately, it is used to classify any compound that meets the Hückel criteria for aromaticity (Section 21.2A).
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Birch reduction
A reaction in which benzene is reduced to give 1,4-cyclohexadiene.
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bond dipole
The dipole moment that is due to unequal electron sharing between two atoms in a covalent bond. (Section 9.3)
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chemical formula.
An expression showing the chemical composition of a compound in terms of the symbols for the atoms of the elements involved. (2.6)
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closest packing.
The most efficient arrangements for packing atoms, molecules, or ions in a crystal. (11.4)
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complete ionic equation
A chemical equation in which dissolved strong electrolytes (such as dissolved ionic compounds) are written as separate ions. (Section 4.2)
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diagonal relationship.
Similarities between pairs of elements in different groups and periods of the periodic table. (8.6)
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Friedel-Crafts reaction
An electrophilic aromatic substitution in which a hydrogen of an aromatic ring is replaced by an alkyl or acyl group.
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furanose
A five-membered cyclic hemiacetal form of a carbohydrate.
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intermetallic compound
A homogeneous alloy with definite properties and a fixed composition. Intermetallic compounds are stoichiometric compounds that form between metallic elements. (Section 12.3)
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Lewis base
A compound capable offunctioning as an electron pair donor.
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metathesis (exchange) reaction
A reaction in which two substances react through an exchange of their component ions: AX + BY ¡ AY + BX. Precipitation and acid–base neutralization reactions are examples of metathesis reactions. (Section 4.2)
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nitronium ion
The NO2+ ion, which is present in a mixture of nitric acid and sulfuric acid.
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norbornane
The common name for bicyclo[2.2.1]heptane.
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Optically active
Refers to a compound that rotates the plane of plane-polarized light
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Quaternary structure
The arrangement of polypeptide monomers into a noncovalently bonded aggregate.
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reaction rate
A measure of the decrease in concentration of a reactant or the increase in concentration of a product with time. (Section 14.2)
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saponification
The base-catalyzed hydrolysis of an ester. This method is used to make soap.
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Trans
A prefi x meaning across from.