Solutions for Chapter 23.5SE: 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 23.5SE

Solutions for Chapter 23.5SE
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Chapter 23.5SE includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Since 2 problems in chapter 23.5SE have been answered, more than 146232 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417.

Key Chemistry Terms and definitions covered in this textbook
  • activate

    For a substituted aromatic ring, the effect of an electron-donating substituent that increases the rate of electrophilic aromatic substitution.

  • aromatic hydrocarbons

    Hydrocarbon compounds that contain a planar, cyclic arrangement of carbon atoms linked by both s and delocalized p bonds. (Section 24.2)

  • b-Pleated sheet

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

  • bimolecular

    For mechanisms, a step that involves two chemical entities.

  • 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.

  • crystal-field theory

    A theory that accounts for the colors and the magnetic and other properties of transition-metal complexes in terms of the splitting of the energies of metal ion d orbitals by the electrostatic interaction with the ligands. (Section 23.6)

  • Decarboxylation

    Loss of CO2 from a carboxyl group.

  • diagonal relationship.

    Similarities between pairs of elements in different groups and periods of the periodic table. (8.6)

  • enantiotopic

    Protons that are not interchangeable by rotational symmetry but are interchangeable by reflectional symmetry.

  • fuel cell

    A voltaic cell that utilizes the oxidation of a conventional fuel, such as H2 or CH4, in the cell reaction. (Section 20.7)

  • Gibbs free energy

    A thermodynamic state function that combines enthalpy and entropy, in the form G = H - TS. For a change occurring at constant temperature and pressure, the change in free energy is ?G = ?H - T?S. (Section 19.5)

  • heterolytic bond cleavage

    Bond breaking that results in the formation of ions.

  • low-spin complex

    A metal complex in which the electrons are paired in lower-energy orbitals. (Section 23.6)

  • Organic synthesis

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

  • parts per million (ppm)

    The concentration of a solution in grams of solute per 106 (million) grams of solution; equals milligrams of solute per liter of solution for aqueous solutions. (Section 13.4)

  • quantitative analysis

    The determination of the amount of a given substance that is present in a sample. (Section 17.7)

  • reducing agent

    A compound that reduces another compound and in the process is itself oxidized. Sodium borohydride and lithium aluminum hydride are reducing agents.

  • second-order reaction

    A reaction in which the overall reaction order (the sum of the concentration- term exponents) in the rate law is 2. (Section 14.4)

  • sulfonation

    An electrophilic aromatic substitution reaction in which an SO3H group is installed on an aromatic ring.

  • torsional strain

    The difference in energy between staggered and eclipsed conformations (for example, in ethane).

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