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Solutions for Chapter 19: Oxidation-Reduction Reactions

Modern Chemistry | 1st Edition | ISBN: 9780030735462 | Authors: Rinehart & Winston Holt

Full solutions for Modern Chemistry | 1st Edition

ISBN: 9780030735462

Modern Chemistry | 1st Edition | ISBN: 9780030735462 | Authors: Rinehart & Winston Holt

Solutions for Chapter 19: Oxidation-Reduction Reactions

Solutions for Chapter 19
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Textbook: Modern Chemistry
Edition: 1
Author: Rinehart & Winston Holt
ISBN: 9780030735462

Modern Chemistry was written by Patricia and is associated to the ISBN: 9780030735462. This textbook survival guide was created for the textbook: Modern Chemistry, edition: 1. Chapter 19: Oxidation-Reduction Reactions includes 31 full step-by-step solutions. Since 31 problems in chapter 19: Oxidation-Reduction Reactions have been answered, more than 4684 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alkali metals

    Members of group 1A in the periodic table. (Section 7.7)

  • Aprotic solvent

    A solvent that cannot serve as a hydrogen-bond donor; nowhere in the molecule is there a hydrogen bonded to an atom of high electronegativity. Common aprotic solvents are dichloromethane, diethyl ether, and dimethyl sulfoxide

  • benzyne

    A high-energy intermediate formed during the elimination-addition reaction that occurs between chlorobenzene and either NaOH (at high temperature) or NaNH2.

  • chemistry

    The scientific discipline that studies the composition, properties, and transformations of matter. (Chapter 1: Introduction)

  • coordinate covalent bond.

    A bond in which the pair of electrons is supplied by one of the two bonded atoms; also called a dative bond. (9.9)

  • Disproportionation

    A termination process that involves the abstraction of a hydrogen atom from the beta position of the propagating radical of one chain by the radical endgroup of another chain.

  • haloalkane

    An organic compound containing at least one halogen.

  • internal alkyne

    A compound with the structure R!C#C!R, where each R group is not a hydrogen atom.

  • meta director

    An electronwithdrawing group that directs the regiochemistry of an electrophilic aromatic substitution reaction such that the incoming electrophile is installed at the meta position.

  • metallic hydrides

    Compounds formed when hydrogen reacts with transition metals; these compounds contain the hydride ion, H-. (Section 22.2)

  • 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)

  • migratory aptitude

    In a BaeyerVilliger oxidation, the migration rates of different groups, which determine the regiochemical outcome of the reaction.

  • nitronium ion

    The NO2+ ion, which is present in a mixture of nitric acid and sulfuric acid.

  • normal melting point

    The melting point at 1 atm pressure. (Section 11.6)

  • overlap

    The extent to which atomic orbitals on different atoms share the same region of space. When the overlap between two orbitals is large, a strong bond may be formed. (Section 9.4)

  • photon

    When electromagnetic radiation is viewed as a particle, an individual packet of energy.

  • rotational motion

    Movement of a molecule as though it is spinning like a top. (Section 19.3)

  • spin-spin splitting

    A phenomenon observed most commonly for nonequivalent protons connected to adjacent carbon atoms, in which the multiplicity of each signal is affected by the other.

  • standard atomic weight

    The weighted averages for each element, which takes into account isotopic abundance.

  • Valence Bond Theory

    A model of bonding that places electron pairs between adjacent atoms to create bonds.

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