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Solutions for Chapter 15.6E: 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 15.6E

Solutions for Chapter 15.6E
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Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 15.6E have been answered, more than 67524 students have viewed full step-by-step solutions from this chapter. Chapter 15.6E includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alkoxide

    The conjugate base of an alcohol.

  • base-dissociation constant (Kb)

    An equilibrium constant that expresses the extent to which a base reacts with solvent water, accepting a proton and forming OH-1aq2. (Section 16.7)

  • body-centered lattice

    A crystal lattice in which the lattice points are located at the center and corners of each unit cell. (Section 12.2)

  • 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.

  • C terminus

    For a peptide chain,the end that contains the COOH group. carbinolamine (Sect. 20.6): A compound containing a hydroxyl group (OH) and a nitrogen atom, both of which are connceted to the same carbon atom.

  • column chromatography

    A technique by which compounds are separated from each other based on a difference in the way they interact with the medium (the adsorbent) through which they are passed.

  • Conjugate acid

    The species formed when a base accepts a proton from an acid

  • Decarboxylation

    Loss of CO2 from a carboxyl group.

  • Dihedral angle

    The angle created by two intersecting planes.

  • Double-headed arrow

    A symbol used to show that structures on either side of it are resonance-contributing structures

  • Frequency

    The number of full cycles of a wave that pass a given point in a second, and reported in hertz (Hz), which has the units s21

  • J value

    When signal splitting occurs in 1H NMR spectroscopy, the distance (in hertz) between the individual peaks of a signal.

  • lattice points

    Points in a crystal all of which have identical environments. (Section 12.2)

  • 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)

  • linkage isomers

    Structural isomers of coordination compounds in which a ligand differs in its mode of attachment to a metal ion. (Section 23.4)

  • octet rule

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

  • rate law

    An equation that relates the reaction rate to the concentrations of reactants (and sometimes of products also). (Section 14.3)

  • reaction order

    The power to which the concentration of a reactant is raised in a rate law. (Section 14.3)

  • reduction

    A process in which a substance gains one or more electrons. (Section 4.4)

  • Soap

    A sodium or potassium salt of a fatty acid

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