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Solutions for Chapter 20: 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 20

Solutions for Chapter 20
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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

Since 239 problems in chapter 20 have been answered, more than 238279 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 20 includes 239 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13.

Key Chemistry Terms and definitions covered in this textbook
  • allylic

    The positions that are adjacent to the vinylic positions of a carboncarbon double bond.

  • aromatic hydrocarbons

    Hydrocarbon compounds that contain a planar, cyclic arrangement of carbon atoms linked by both s and delocalized p bonds. (Section 24.2)

  • Arrhenius equation

    An equation that relates the rate constant for a reaction to the frequency factor, A, the activation energy, Ea, and the temperature, T: k = Ae-Ea>RT. In its logarithmic form it is written ln k = -Ea>RT + ln A. (Section 14.5)

  • atomic mass.

    The mass of an atom in atomic mass units. (3.1)

  • conjugate acid

    A substance formed by addition of a proton to a Brønsted–Lowry base. (Section 16.2)

  • conjugate acid-base pair.

    An acid and its conjugate base or a base and its conjugate acid. (15.1)

  • coplanar

    Atoms that lie in the same plane.

  • electron

    A negatively charged subatomic particle found outside the atomic nucleus; it is a part of all atoms. An electron has a mass 1>1836 times that of a proton. (Section 2.3)

  • Endergonic reaction

    A reaction in which the Gibbs free energy of the products is higher than that of the reactants. The position of equilibrium for an endergonic reaction favors starting materials

  • ignal splitting in NMR

    Spin-spin coupling with adjacent nuclei split NMR signals depending on the extent of coupling and the number of adjacent equivalent nuclei.

  • irreversible process

    A process that cannot be reversed to restore both the system and its surroundings to their original states. Any spontaneous process is irreversible. (Section 19.1)

  • mercapto group

    An SH group.

  • molal freezing-point-depression constant (Kf)

    A constant characteristic of a particular solvent that gives the decrease in freezing point as a function of solution molality: ?Tf = -Kf m. (Section 13.5)

  • Order of precedence of functions

    A ranking of functional groups in order of priority for the purposes of IUPAC nomenclature.

  • Oxonium ion

    An ion in which oxygen bears a positive charge.

  • polyatomic ion

    An electrically charged group of two or more atoms. (Section 2.7)

  • reduction

    A reaction in which a compound undergoes a decrease in oxidation state.

  • sp2 Hybrid orbital

    A hybrid atomic orbital formed by the combination of one s atomic orbital and two 2p atomic orbitals.

  • Synstereoselective

    The addition of atoms or groups of atoms to the same face of a carbon-carbon double bond.

  • Zaitsev product

    The more substituted product (alkene) of an elimination reaction.

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