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Solutions for Chapter 14: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Solutions for Chapter 14

Solutions for Chapter 14
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Textbook: Chemistry: The Central Science
Edition: 13
Author: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus
ISBN: 9780321910417

This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. This expansive textbook survival guide covers the following chapters and their solutions. Since 283 problems in chapter 14 have been answered, more than 243067 students have viewed full step-by-step solutions from this chapter. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Chapter 14 includes 283 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • acceptor impurities.

    Impurities that can accept electrons from semiconductors. (21.3)

  • amide

    An organic compound that has an NR2 group attached to a carbonyl. (Section 24.4)

  • beta (b) position

    The position immediately adjacent to an alpha (a) position.

  • bond cleavage

    The breaking of a bond, either homolytically or heterolytically. bond dissociation energy (Sect. 6.1): The energy required to achieve homolytic bond cleavage (generating radicals).

  • chemical nomenclature

    The rules used in naming substances. (Section 2.8)

  • condensation polymerization

    Polymerization in which molecules are joined together through condensation reactions. (Section 12.8)

  • Cope rearrangement

    A [3,3] sigmatropic rearrangement in which all six atoms of the cyclic transition state are carbon atoms.

  • electron affinity

    The energy change that occurs when an electron is added to a gaseous atom or ion. (Section 7.5)

  • flagpole interactions

    For cyclohexane, the steric interactions that occur between the flagpole hydrogen atoms in a boat conformation.

  • Haloarene (aryl halide)

    A compound containing a halogen atom bonded to a benzene ring. Given the symbol Ar!X

  • isoelectronic series

    A series of atoms, ions, or molecules having the same number of electrons. (Section 7.3)

  • labile

    Protons that are exchanged at a rapid rate.

  • ligand

    An ion or molecule that coordinates to a metal atom or to a metal ion to form a complex. (Section 23.2)

  • mass spectrometry

    The study ofthe interaction between matter and an energysource other than electromagnetic radiation. Massspectrometry is used primarily to determine the molecular weight and molecular formula of a compound.

  • molecular hydrides

    Compounds formed when hydrogen reacts with nonmetals and metalloids. (Section 22.2)

  • oligomers

    During the polymerization process, compounds constructed from just a few monomers.

  • quantitative analysis

    The determination of the amount of a given substance that is present in a sample. (Section 17.7)

  • reducing sugar

    A carbohydrate that is oxidized upon treatment with Tollens’ reagent, Fehling’s reagent, or Benedict’s reagent.

  • sigma 1S2 bond

    A covalent bond in which electron density is concentrated along the internuclear axis. (Section 9.6)

  • Tautomers

    Constitutional isomers in equilibrium with each other that differ in the location of a hydrogen atom and a double bond relative to a heteroatom, most commonly O, N, or S.

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