Solutions for Chapter 14.9SE: 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 14.9SE

Solutions for Chapter 14.9SE
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Chapter 14.9SE includes 2 full step-by-step solutions. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. 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. Since 2 problems in chapter 14.9SE have been answered, more than 146716 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • acylium ion

    The resonancestabilized, cationic intermediate of a Friedel-Crafts acylation, formed by treating an acyl halide with aluminum trichloride.

  • anti-periplanar

    A conformation in which a hydrogen atom and a leaving group are separated by a dihedral angle of approximately 180°.

  • autooxidation

    The slow oxidation of organic compounds that occurs in the presence of atmospheric oxygen.

  • b-Pleated sheet

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

  • chemical nomenclature

    The rules used in naming substances. (Section 2.8)

  • conversion factor

    A ratio relating the same quantity in two systems of units that is used to convert the units of measurement. (Section 1.6)

  • copolymer.

    A polymer containing two or more different monomers. (25.2)

  • desalination

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

  • dilution

    The process of preparing a less concentrated solution from a more concentrated one by adding solvent. (Section 4.5)

  • elimination (of radicals)

    In radical reaction mechanisms, a step in which a bond forms between the alpha (a) and beta (b) positions. As a result, a single bond at the b position is cleaved, causing the compound to fragment into two pieces.

  • epimer

    Diastereomers that differ from each other in the configuration of only one chirality center.

  • Exergonic reaction

    A reaction in which the Gibbs free energy of the products is lower than that of the reactants. The position of equilibrium for an exergonic reaction favors products.

  • Heat of reaction (DH0 )

    The difference in enthalpy between reactants and products. If the enthalpy of products is lower than that of the reactants, heat is released and the reaction is exothermic. If the enthalpy of the products is higher than that of the reactants, energy is absorbed, and the reaction is endothermic

  • magnetic moment

    A magneticfield generated by a spinning proton.

  • main-group elements

    Elements in the s and p blocks of the periodic table. (Section 6.9)

  • Michael donor

    The nucleophile in a Michael reaction.

  • Node

    A point in space where the value of a wave function is zero

  • octet rule

    The observation that second-row elements (C, N, O, and F) will form the necessary number of bonds so as to achieve a full valence shell (eight electrons).

  • regioselective

    A reaction that can produce two or more constitutional isomers but nevertheless produces one as the major product.

  • Triglyceride (triacylglycerol)

    An ester of glycerol with three fatty acids

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