Solutions for Chapter 18.4: Solubility Equilibrium

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 18.4: Solubility Equilibrium

Modern Chemistry: Student Edition 2012 was written by Patricia and is associated to the ISBN: 9780547586632. This textbook survival guide was created for the textbook: Modern Chemistry: Student Edition 2012, edition: 1. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 18.4: Solubility Equilibrium includes 7 full step-by-step solutions. Since 7 problems in chapter 18.4: Solubility Equilibrium have been answered, more than 22592 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • 1,4-adduct

    The product obtained from 1,4-addition across a conjugated p system.

  • chain reaction

    A series of reactions in which one reaction initiates the next. (Section 21.7)

  • diene

    A compound containing two carbon-carbon p bonds.

  • dipole

    A molecule with one end having a partial negative charge and the other end having a partial positive charge; a polar molecule. (Section 8.4)

  • disulfide

    A compound with the structure R!S!S!R.

  • Elastomer

    A material that, when stretched or otherwise distorted, returns to its original shape when the distorting force is released.

  • electron

    A negatively charged subatomic particle found outside the atomic nucleus; it is a part of all atoms. An electron has a mass 1>1836 times that of a proton. (Section 2.3)

  • fibrous proteins

    Proteins that consist of linear chains that are bundled together.

  • Haworth projection

    For substituted cycloalkanes, a drawing style used to clearly identify which groups are above the ring and which groups are below the ring. (See also Sect. 4.14.)

  • Homotopic groups

    Atoms or groups on an atom that give an achiral molecule when one of the groups is replaced by another group. The hydrogens of the CH2 group of propane, for example, are homotopic. Replacing either one of them with deuterium gives 2-deuteropropane, which is achiral. Homotopic groups have identical chemical shifts under all conditions

  • inversion of configuration

    During a reaction, when the configuration of a chirality center is changed.

  • Lewis acid

    A compound capable offunctioning as an electron pair acceptor.

  • nomenclature

    A system for naming organic compounds.

  • Organic synthesis

    A series of reactions by which a set of organic starting materials is converted to a more complicated structure.

  • pressure–volume (PV) work

    Work performed by expansion of a gas against a resisting pressure. (Section 5.3)

  • primary cell

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

  • S (Section 3.3

    From the Latin, sinister, left; used in the R,S convention to show that the order of priority of groups on a chiral center is counterclockwise

  • Secondary (2°) amine

    An amine in which nitrogen is bonded to two carbons and one hydrogen

  • Secondary structure of nucleic acids

    The ordered arrangement of nucleic acid strands

  • 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.

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