Solutions for Chapter 10.12SE: 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 10.12SE

Solutions for Chapter 10.12SE
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Chapter 10.12SE includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 10.12SE have been answered, more than 108667 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • amphiprotic

    Refers to the capacity of a substance to either add or lose a proton 1H+2. (Section 16.2)

  • binary compounds.

    Compounds formed from just two elements. (2.7)

  • bond dipole

    The dipole moment that is due to unequal electron sharing between two atoms in a covalent bond. (Section 9.3)

  • core electrons.

    All nonvalence electrons in an atom. (8.2)

  • covalent bond

    A bond that results when two atoms share a pair of electrons.

  • Deshielding

    The term used to express the concept of less shielding in NMR

  • folding

    The process by which a protein adopts its biologically active shape. (Section 24.7)

  • Gibbs free energy (G)

    The ultimate arbiter of the spontaneity of a reaction, where DG = DH - T DS.

  • hydrohalogenation

    A reaction that involves the addition of H and X (either Br or Cl) across an alkene.

  • internal alkyne

    A compound with the structure R!C#C!R, where each R group is not a hydrogen atom.

  • ionic reaction

    A reaction that involves the participation of ions as reactants, intermediates, or products.

  • Lewis structure

    A representation of covalent bonding in a molecule that is drawn using Lewis symbols. Shared electron pairs are shown as lines, and unshared electron pairs are shown as pairs of dots. Only the valence-shell electrons are shown. (Section 8.3)

  • N-bromosuccinimide

    A reagent used for allylic bromination to avoid a competing reaction in which bromine adds across the p bond.

  • nuclear magnetic resonance (NMR)

    A form of spectroscopy that involves the study of the interaction between electromagnetic radiation and the nuclei of atoms.

  • Nucleophilic substitution

    Any reaction in which one nucleophile is substituted for another at a tetravalent carbon atom.

  • phenolate

    The conjugate base of phenol or a substituted phenol.

  • Plane of symmetry

    An imaginary plane passing through an object dividing it so that one half is the mirror image of the other half

  • polymer

    A large molecule of high molecular mass, formed by the joining together, or polymerization, of a large number of molecules of low molecular mass. The individual molecules forming the polymer are called monomers. (Sections 12.1 and 12.8)

  • spontaneous process

    A process that is capable of proceeding in a given direction, as written or described, without needing to be driven by an outside source of energy. A process may be spontaneous even though it is very slow. (Section 19.1)

  • symmetry forbidden

    A reaction that disobeys conservation of orbital symmetry.

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