- Chapter 1: Matter and Change
- Chapter 10: States of Matter
- Chapter 11: Gases
- Chapter 12: Solutions
- Chapter 13: Ions in Aqueous Solutions and Coiigative Properties
- Chapter 14: Acids and Bases
- Chapter 15: Acid-Base Titration andpH
- Chapter 16: Reaction Energy
- Chapter 17: Reaction Kinetics
- Chapter 18: Chemical Equilibrium
- Chapter 19: Oxidation-Reduction Reactions
- Chapter 2: Measurements and Calculations
- Chapter 20: Electrochemistry
- Chapter 21: Nuclear Chemistry
- Chapter 22: Organic Chemistry
- Chapter 23: Biological Chemistry
- Chapter 3: Atoms: The Building Blocks ofMatter
- Chapter 4: Arrangement of Electrons in Atoms
- Chapter 5: The Periodic Law
- Chapter 6: Chemical Bonding
- Chapter 7: Chemical Formulas and Chemical Compounds
- Chapter 8: Chemical Equations andReactions
- Chapter 9: Stoichiometry
Modern Chemistry 1st Edition - Solutions by Chapter
Full solutions for Modern Chemistry | 1st Edition
A polyaromatic amide; a polymer in which the monomer units are an aromatic diamine and an aromatic dicarboxylic acid
In UV-Vis spectroscopy, the region of the molecule responsible for the absorption (the conjugated p system).
A three-dimensional shape that can be adopted by a compound as a result of rotation about single bonds.
dextrorotatory, or merely dextro or d
A term used to label a chiral molecule that rotates the plane of polarization of plane-polarized light to the right (clockwise). (Section 23.4)
Stereoisomers that are not mirror images of one another.
The use of electrolysis to reduce or refine metals. (Section 20.9)
A collection of orbitals that have the same value of n. For example, the orbitals with n = 3 (the 3s, 3p, and 3d orbitals) comprise the third shell. (Section 6.5)
Any process with a positive DH (the system receives energy from the surroundings).
The attractive forces between molecules.
A term that refers to the rate of a reaction.
During the polymerization process, compounds constructed from just a few monomers.
A form of isomerism in which the two forms of a compound (stereoisomers) are nonsuperimposable mirror images. (Section 23.4)
A reaction that takes place in a single step, without intermediates, and involves a cyclic redistribution of bonding electrons
A mixture of equal amounts of the dextrorotatory and levorotatory forms of a chiral molecule. A racemic mixture will not rotate the plane of polarized light. (Section 23.4)
A measure of the energy absorbed from radiation by tissue or other biological material; 1 rad = transfer of 1 * 10-2 J of energy per kilogram of material. (Section 21.9)
A reaction in which a compound undergoes a decrease in oxidation state.
A process in which a substance gains one or more electrons. (Section 4.4)
Secondary (2°) amine
An amine in which nitrogen is bonded to two carbons and one hydrogen
The outermost occupied electron shell of an atom.
A method for converting a carbonyl group into a methylene group (CH2) under basic conditions.