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 25046 students have viewed full step-by-step solutions from this chapter. Modern Chemistry: Student Edition 2012 was written by 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
  • amphoteric

    Compounds that will react with either acids or bases. Amino acids are amphoteric.

  • antibonding molecular orbital

    A molecular orbital in which electron density is concentrated outside the region between the two nuclei of bonded atoms. Such orbitals, designated as s* or p*, are less stable (of higher energy) than bonding molecular orbitals. (Section 9.7)

  • bidentate ligand

    A ligand in which two linked coordinating atoms are bound to a metal. (Section 23.3)

  • Brønsted-Lowry base

    A compound that can serve as a proton acceptor.

  • Conjugation

    A situation in which two multiple bonds are separated by a single bond. Alternatively, a series of overlapping 2p orbitals. 1,3-butadiene, for example, is a conjugated diene, and 3-butene-2-one is a conjugated enone

  • desalination

    The removal of salts from seawater, brine, or brackish water to make it fit for human consumption. (Section 18.4)

  • Endothermic reaction

    A reaction in which the enthalpy of the products is higher than the enthalpy of the reactants; a reaction in which heat is absorbed

  • Formal charge

    The charge on an atom in a polyatomic ion or molecule

  • heterogeneous catalyst

    A catalyst that does not dissolve in the reaction medium.

  • Isotactic polymer

    A polymer with identical confi gurations (either all R or all S) at all chiral centers along its chain, as, for example, isotactic polypropylene

  • kinetic control

    A reaction for which the product distribution is determined by the relative rates at which the products are formed.

  • Lewis acid

    Any molecule or ion that can form a new covalent bond by accepting a pair of electrons.

  • molality

    The concentration of a solution expressed as moles of solute per kilogram of solvent; abbreviated m. (Section 13.4)

  • Para (p)

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

  • polycarbonates

    Polymers that are similar in structure to polyesters but with repeating carbonate groups (!O!CO2!) instead of repeating ester groups (!CO2!). polycyclic aromatic hydrocarbons

  • primary cell

    A voltaic cell that cannot be recharged. (Section 20.7)

  • reducing sugar

    A carbohydrate that is oxidized upon treatment with Tollens’ reagent, Fehling’s reagent, or Benedict’s reagent.

  • specific heat 1Cs2

    The heat capacity of 1 g of a substance; the heat required to raise the temperature of 1 g of a substance by 1 °C. (Section 5.5)

  • sulfone

    A compound that contains a sulfur atom that has double bonds with two oxygen atoms and is flanked on both sides by R groups.

  • trivalent

    An element, such as nitrogen, that forms three bonds.

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