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Solutions for Chapter 20: The Nucleus: A Chemists View

Chemical Principles | 8th Edition | ISBN: 9781305581982 | Authors: Steven S. Zumdahl

Full solutions for Chemical Principles | 8th Edition

ISBN: 9781305581982

Chemical Principles | 8th Edition | ISBN: 9781305581982 | Authors: Steven S. Zumdahl

Solutions for Chapter 20: The Nucleus: A Chemists View

Solutions for Chapter 20
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Textbook: Chemical Principles
Edition: 8
Author: Steven S. Zumdahl
ISBN: 9781305581982

Chapter 20: The Nucleus: A Chemists View includes 86 full step-by-step solutions. Since 86 problems in chapter 20: The Nucleus: A Chemists View have been answered, more than 49461 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Chemical Principles, edition: 8. This expansive textbook survival guide covers the following chapters and their solutions. Chemical Principles was written by and is associated to the ISBN: 9781305581982.

Key Chemistry Terms and definitions covered in this textbook
  • acetoacetic ester synthesis

    A threestep process that converts an alkyl halide into a methyl ketone with the introduction of three new carbon atoms.

  • aldose

    A carbohydrate that contains an aldehyde group.

  • Amorphous domain

    A disordered, noncrystalline region in the solid state of a polymer.

  • anti addition

    An addition reaction in which two groups are installed on opposite sides of a p bond.

  • carboxylic acid

    A compound that contains the ¬COOH functional group. (Sections 16.10 and 24.4)

  • cathode

    An electrode at which reduction occurs. (Section 20.3)

  • chemical properties

    Properties that describe a substance’s composition and its reactivity; how the substance reacts or changes into other substances. (Section 1.3)

  • electrometallurgy

    The use of electrolysis to reduce or refine metals. (Section 20.9)

  • face-centered lattice

    A crystal lattice in which the lattice points are located at the faces and corners of each unit cell. (Section 12.2)

  • frontier orbital theory

    The analysis of a reaction using MO theory, where only the frontier orbitals (HOMO and LUMO) are considered.

  • functional group

    A characteristic group of atoms/bonds that possess a predictable chemical behavior.

  • ionic compound

    A compound composed of cations and anions. (Section 2.7)

  • mean free path

    The average distance traveled by a gas molecule between collisions. (Section 10.8)

  • observed rotation

    The extent to which plane-polarized light is rotated by a solution of a chiral compound.

  • Octet rule

    Group 1A–7A elements react to achieve an outer shell of eight valence electrons.

  • Oxymercuration-reduction

    A method for converting an alkene to an alcohol. The alkene is treated with mercury(II) acetate followed by reduction with sodium borohydride.

  • prosthetic group

    A nonprotein unit attached to a protein, such as heme in hemoglobin.

  • step-growth polymers

    Polymers that are formed under conditions in which the individual monomers react with each other to form oligomers, which are then joined together to form polymers.

  • Terpene

    A compound whose carbon skeleton can be divided into two or more units identical with the carbon skeleton of isoprene

  • upfield

    The right side of an NMRspectrum.

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