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Solutions for Chapter 5.2: ElectronConfiguration andthe Periodic Table

Modern Chemistry: Student Edition 2012 | 1st Edition | ISBN: 9780547586632 | Authors: Jerry L. Sarquis, Mickey Sarquis

Full solutions for Modern Chemistry: Student Edition 2012 | 1st Edition

ISBN: 9780547586632

Modern Chemistry: Student Edition 2012 | 1st Edition | ISBN: 9780547586632 | Authors: Jerry L. Sarquis, Mickey Sarquis

Solutions for Chapter 5.2: ElectronConfiguration andthe Periodic Table

This expansive textbook survival guide covers the following chapters and their solutions. Since 6 problems in chapter 5.2: ElectronConfiguration andthe Periodic Table have been answered, more than 14181 students have viewed full step-by-step solutions from this chapter. Modern Chemistry: Student Edition 2012 was written by Patricia and is associated to the ISBN: 9780547586632. Chapter 5.2: ElectronConfiguration andthe Periodic Table includes 6 full step-by-step solutions. This textbook survival guide was created for the textbook: Modern Chemistry: Student Edition 2012, edition: 1.

Key Chemistry Terms and definitions covered in this textbook
  • actinide series.

    Elements that have incompletely filled 5f subshells or readily give rise to cations that have incompletely filled 5f subshells. (7.9)

  • atactic

    A polymer in which the repeating units contain chirality centers which are not arranged in a pattern (they have random configurations).

  • beta emission

    A nuclear decay process where a beta particle is emitted from the nucleus; also called beta decay. (Section 21.1)

  • blocking group

    A group that can be readily installed and uninstalled. Used for regiochemical control during synthesis.

  • chemical formula.

    An expression showing the chemical composition of a compound in terms of the symbols for the atoms of the elements involved. (2.6)

  • core electrons.

    All nonvalence electrons in an atom. (8.2)

  • Deactivating group

    Any substituent on a benzene ring that causes the rate of electrophilic aromatic substitution to be lower than that for benzene.

  • exchange (metathesis) reaction

    A reaction between compounds that when written as a molecular equation appears to involve the exchange of ions between the two reactants. (Section 4.2)

  • leveling effect

    An effect thatprevents the use of bases stronger than hydroxidewhen the solvent is water.

  • metallic solids

    Solids that are composed of metal atoms. (Section 12.1)

  • molecular-orbital theory

    A theory that accounts for the allowed states for electrons in molecules.(Section 9.7)

  • Monomer

    From the Greek, mono 1 meros, meaning single part. The simplest nonredundant unit from which a polymer is synthesized.

  • nonmetallic elements (nonmetals)

    Elements in the upper right corner of the periodic table; nonmetals differ from metals in their physical and chemical properties. (Section 2.5)

  • organohalide

    An organic compound containing at least one halogen.

  • Para (p)

    Refers to groups occupying l,4-positions on a benzene ring

  • phosphoglycerides

    Compounds that are very similar in structure to triglycerides, with the main difference being that one of the three fatty acid residues is replaced by a phosphoester group.

  • Radical inhibitor

    A compound such as a phenol that selectively reacts with radicals to remove them from a chain reaction and terminate the chain

  • Sigma (s) molecular orbital

    A molecular orbital in which electron density is concentrated between two nuclei, along the axis joining them, and is cylindrically symmetrical

  • syn addition

    An addition reaction in which two groups are added to the same face of a p bond.

  • Wittig reagent

    A reagent used to perform a Wittig reaction.

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