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Solutions for Chapter 4.3: Electron Configurations

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 4.3: Electron Configurations

Chapter 4.3: Electron Configurations includes 6 full step-by-step solutions. Modern Chemistry: Student Edition 2012 was written by and is associated to the ISBN: 9780547586632. This textbook survival guide was created for the textbook: Modern Chemistry: Student Edition 2012, edition: 1. Since 6 problems in chapter 4.3: Electron Configurations have been answered, more than 51619 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
  • alkenes.

    Hydrocarbons that contain one or more carbon-carbon double bonds. They have the general formula CnH2n, where n 5 2,3, . . . . (24.2)

  • alkyl group

    A substituent lacking p bonds and comprised of only carbon and hydrogen atoms.

  • allylic carbocation

    A carbocation in which the positive charge is adjacent to a carbon-carbon double bond.

  • aqueous solution

    A solution in which water is the solvent. (Chapter 4: Introduction)

  • bimolecular reaction.

    An elementary step that involves two molecules. (13.5)

  • biochemistry

    The study of the chemistry of living systems. (Chapter 24: Introduction)

  • cephalins

    Phosphoglycerides that contain ethanolamine.

  • condensation reaction

    A chemical reaction in which a small molecule (such as a molecule of water) is split out from between two reacting molecules. (Sections 12.6 and 22.8)

  • Confi gurational isomers

    Isomers that differ by the confi guration of substituents on an atom. Refers to the arrangement of atoms about a stereocenter

  • dihydroxylation

    A reaction characterized by the addition of two hydroxyl groups (OH) across an alkene.

  • electrolyte

    A solute that produces ions in solution; an electrolytic solution conducts an electric current. (Section 4.1)

  • hydroperoxide

    A compound with the structure R!O!O!H.

  • immiscible liquids

    Liquids that do not dissolve in one another to a significant extent. (Section 13.3)

  • London dispersion forces

    Attractive forces between transient dipole moments, observed in alkanes.

  • Micelle

    A spherical arrangement of organic molecules in water solution clustered so that their hydrophobic parts are buried inside the sphere and their hydrophilic parts are on the surface of the sphere and in contact with water

  • molecule

    A chemical combination of two or more atoms. (Sections 1.1 and 2.6)

  • octet rule

    A rule stating that bonded atoms tend to possess or share a total of eight valence-shell electrons. (Section 8.1)

  • Pauli exclusion principle

    The rule that states that an atomic orbital or molecular orbital can accommodate a maximum of two electrons with opposite spin.

  • peptidases

    A variety of enzymes that selectively hydrolyze specific peptide bonds.

  • Trans

    A prefi x meaning across from.

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