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Solutions for Chapter 24.2SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

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

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Solutions for Chapter 24.2SE

Solutions for Chapter 24.2SE
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This expansive textbook survival guide covers the following chapters and their solutions. Chapter 24.2SE 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 24.2SE have been answered, more than 264185 students have viewed full step-by-step solutions from this chapter. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417.

Key Chemistry Terms and definitions covered in this textbook
  • alkene

    A compound that possesses a carbon-carbon double bond.

  • asymmetric stretching

    In IR spectroscopy, when two bonds are stretching out of phase with each other.

  • beta particles.

    See beta rays.

  • bond length

    The distance between the centers of two bonded atoms. (Section 8.3)

  • bond order

    The number of bonding electron pairs shared between two atoms, minus the number of antibonding electron pairs: bond order = (number of bonding electrons - number of antibonding electrons)/2. (Section 9.7)

  • cell voltage.

    Difference in electrical potential between the anode and the cathode of a galvanic cell. (18.2)

  • colligative properties.

    Properties of solutions that depend on the number of solute particles in solution and not on the nature of the solute particles. (12.6)

  • elimination-addition

    A reaction that occurs between chlorobenzene and either NaOH (at high temperature) or NaNH2.

  • isotopes

    Atoms of the same element containing different numbers of neutrons and therefore having different masses. (Section 2.3)

  • main-group elements

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

  • Newman projection

    A way to view a molecule by looking along a carbon-carbon single bond

  • nomenclature

    A system for naming organic compounds.

  • nucleophile

    A compound containing an electron-rich atom that is capable of donating a pair of electrons.

  • polypeptide

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

  • Polyunsaturated triglyceride

    A triglyceride having several carbon-carbon double bonds in the hydrocarbon chains of its three fatty acids.

  • propagation

    For radical reactions,the steps whose sum gives the net chemical reaction.

  • Solvolysis

    A nucleophilic substitution in which the solvent is also the nucleophile

  • stereospecific

    A reaction in which the configuration of the product is dependent on the configuration of the starting material.

  • Sulfi de

    The sulfur analog of an ether; a molecule containing a sulfur atom bonded to two carbon atoms. Sulfi des are also called thioethers

  • Wittig reaction

    A reaction that converts an aldehyde or ketone into an alkene, with the introduction of one or more carbon atoms.

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