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Solutions for Chapter 4.5SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Solutions for Chapter 4.5SE

Solutions for Chapter 4.5SE
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Since 2 problems in chapter 4.5SE have been answered, more than 67734 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chapter 4.5SE includes 2 full step-by-step solutions. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • acceptor impurities.

    Impurities that can accept electrons from semiconductors. (21.3)

  • alkane

    A hydrocarbon that lacks p bonds.

  • alkoxide

    The conjugate base of an alcohol.

  • alkylthio group

    An SR group.

  • Avogadro’s law.

    At constant pressure and temperature, the volume of a gas is directly proportional to the number of moles of the gas present. (5.3)

  • b-Pleated sheet

    A type of polypeptide secondary structure in which sections of polypeptide chains are aligned parallel or antiparallel to one another.

  • boat conformation

    A conformation of cyclohexane in which all bond angles are fairly close to 109.5° and many hydrogen atoms are eclipsing each other.

  • bond-line structures

    The most common drawing style employed by organic chemists. All carbon atoms and most hydrogen atoms are implied but not explicitly drawn in a bond-line structure.

  • elastomers

    Polymers that return to their original shape after being stretched.

  • ether

    A compound in which two hydrocarbon groups are bonded to one oxygen. (Section 24.4)

  • hydrogen abstraction

    In radical reactions, a type of arrow-pushing pattern in which a hydrogen atom is abstracted by a radical, generating a new radical.

  • law of constant composition

    A law that states that the elemental composition of a pure compound is always the same, regardless of its source; also called the law of definite proportions. (Section 1.2)

  • Mass spectrometry

    An analytical technique for measuring the mass-to-charge ratio (m/z) of ions.

  • miscible liquids

    Liquids that mix in all proportions. (Section 13.3)

  • Polyamide

    A polymer in which each monomer unit is joined to the next by an amide bond, as, for example, nylon 66.

  • polypeptide

    A polymer of amino acids that has a molecular weight of less than 10,000. (Section 24.7)

  • redox (oxidation–reduction) reaction

    A reaction in which certain atoms undergo changes in oxidation states. The substance increasing in oxidation state is oxidized; the substance decreasing in oxidation state is reduced. (Section 4.4; Chapter 20: Introduction)

  • secondary structure

    The manner in which a protein is coiled or stretched. (Section 24.7)

  • silica

    Common name for silicon dioxide. (Section 22.4)

  • spectrochemical series

    A list of ligands arranged in order of their abilities to split the d-orbital energies (using the terminology of the crystal-field model). (Section 23.6)

Textbook Survival Guides

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