Solutions for Chapter 15.12SE: 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 15.12SE

Solutions for Chapter 15.12SE
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Since 2 problems in chapter 15.12SE have been answered, more than 141805 students have viewed full step-by-step solutions from this chapter. Chapter 15.12SE includes 2 full step-by-step solutions. 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. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13.

Key Chemistry Terms and definitions covered in this textbook
  • anti addition

    An addition reaction in which two groups are installed on opposite sides of a p bond.

  • atmosphere (atm)

    A unit of pressure equal to 760 torr; 1 atm = 101.325 kPa. (Section 10.2) atom The smallest representative particle of an element. (Sections 1.1 and 2.1)

  • bond length.

    The distance between the nuclei of two bonded atoms in a molecule. (9.4)

  • Chemical shift (d)

    The shift in parts per million of an NMR signal relative to the signal of TMS

  • covalent compounds.

    Compounds containing only covalent bonds. (9.4)

  • doping

    Incorporation of a hetero atom into a solid to change its electrical properties. For example, incorporation of P into Si. (Section 12.7)

  • Enol

    A compound containing a hydroxyl group bonded to a doubly bonded carbon atom.

  • green chemistry

    Chemistry that promotes the design and application of chemical products and processes that are compatible with human health and that preserve the environment. (Section 18.5)

  • hydrate

    A compound containing two hydroxyl groups (OH) connected to the same carbon atom.

  • ideal solution

    A solution that obeys Raoult’s law. (Section 13.5)

  • meta

    On an aromatic ring, the C3 position.

  • mixture

    A combination of two or more substances in which each substance retains its own chemical identity. (Section 1.2)

  • nucleosides

    The product formed when either d-ribose or 2-deoxy-d-ribose is coupled with certain nitrogen heterocycles (called bases).

  • potential energy

    The energy that an object possesses as a result of its composition or its position with respect to another object. (Section 5.1)

  • resonance hybrid

    A term used to describe the character of a chemical entity (molecule, ion, or radical) exhibiting more than one significant resonance structure.

  • sp3 Hybrid orbital

    A hybrid atomic orbital formed by the combination of one s atomic orbital and three 2p atomic orbitals.

  • Stork enamine synthesis

    A Michaelreaction in which an enamine functions as anucleophile.

  • substitution reactions

    Reactions in which one group is replaced by another group.

  • torsional angle

    The angle between two groups in a Newman projection, also called the dihedral angle.

  • Upfield

    A signal of an NMR spectrum that is shifted toward the right (smaller chemical shift) on the chart paper.

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