- 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
The pressure exerted by Earth’s atmosphere. (5.2)
A statement that the volume of a gas maintained at constant temperature and pressure is directly proportional to the number of moles of the gas. (Section 10.3)
The light absorbed by a substance (A) equals the product of its extinction coefficient 1e2, the path length through which the light passes (b), and the molar concentration of the substance (c): A = ebc. (Section 14.2)
The distance between atoms in a covalent bond in picometers (pm; 1 pm 5 10212 m) or Å (1Å 5 10210 m).
A spectrum that contains radiation distributed over all wavelengths. (Section 6.3)
B2H6. A dimeric structure formed when one borane molecule reacts with another.
The atom of a ligand that bonds to the metal. (Section 23.2)
A nonsuperimposable mirror image.
For cyclohexane, the steric interactions that occur between the flagpole hydrogen atoms in a boat conformation.
An organic compound containing at least one halogen.
Haloarene (aryl halide)
A compound containing a halogen atom bonded to a benzene ring. Given the symbol Ar!X
Protons that are interchangeable by rotational symmetry.
An effect that explains why alkyl groups stabilize a carbocation.
A process by which the chain of a carbohydrate is lengthened by one carbon atom.
A back-to-back arrangement of phospholipid monolayers, often forming a closed vesicle or membrane.
An instrument used to measure the precise masses and relative amounts of atomic and molecular ions. (Section 2.4)
Theresonance-stabilized intermediate of a nucleophilicaromatic substitution reaction.
A biopolymer containing three types of monomer units: heterocyclic aromatic amine bases derived from purine and pyrimidine, the monosaccharides d-ribose or 2-deoxy-d-ribose, and phosphoric acid
A characteristic that gives a sample of matter its unique identity. (Section 1.1)
For alkenes, a stereodescriptor that indicates that the two priority groups are on the same side of the p bond.