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Solutions for Chapter 14.14SE: 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 14.14SE

Solutions for Chapter 14.14SE
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This expansive textbook survival guide covers the following chapters and their solutions. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chapter 14.14SE includes 2 full step-by-step solutions. Since 2 problems in chapter 14.14SE have been answered, more than 67668 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • aldehyde

    An organic compound that contains a carbonyl group 1C “O2 to which at least one hydrogen atom is attached. (Section 24.4)

  • Alkene metathesis

    A reaction in which two alkenes interchange the carbons attached to their double bonds.

  • alloy

    A substance that has the characteristic properties of a metal and contains more than one element. Often there is one principal metallic component, with other elements present in smaller amounts. Alloys may be homogeneous or heterogeneous. (Section 12.3)

  • Avogadro’s law

    A statement that the volume of a gas maintained at constant temperature and pressure is directly proportional to the number of moles of the gas. (Section 10.3)

  • axial position

    For chair conformations of substituted cyclohexanes, a position that is parallel to a vertical axis passing through the center of the ring.

  • chemical energy.

    Energy stored within the structural units of chemical substances. (6.1)

  • cycloalkanes.

    Alkanes whose carbon atoms are joined in rings. (24.2)

  • deposition.

    The process in which the molecules go directly from the vapor into the solid phase. (11.8)

  • electrolytic cell

    A device in which a nonspontaneous oxidation–reduction reaction is caused to occur by passage of current under a sufficient external electrical potential. (Section 20.9)

  • free induction decay

    In NMR spectroscopy, a complex signal which is a combination of all of the electrical impulses generated by each type of proton.

  • halohydrin formation

    A reaction which involves the addition of a halogen and a hydroxyl group (OH) across an alkene.

  • liquid crystal

    A substance that exhibits one or more partially ordered liquid phases above the melting point of the solid form. By contrast, in nonliquid crystalline substances the liquid phase that forms upon melting is completely unordered. (Section 11.7)

  • Living polymer

    A polymer chain that continues to grow without chain-termination steps until either all of the monomer is consumed or some external agent is added to terminate the chain. The polymer chains will continue to grow if more monomer is added.

  • Mass spectrometry

    An analytical technique for measuring the mass-to-charge ratio (m/z) of ions.

  • molecular orbital (MO)

    An allowed state for an electron in a molecule. According to molecular-orbital theory, a molecular orbital is entirely analogous to an atomic orbital, which is an allowed state for an electron in an atom. Most bonding molecular orbitals can be classified as s or p, depending on the disposition of electron density with respect to the internuclear axis. (Section 9.7)

  • Phenol

    A compound that contains an !OH bonded to a benzene ring; a benzenol.

  • polarizability

    The ability of an atom or molecule to distribute its electron density unevenly in response to external influences.

  • Polypeptide

    A macromolecule containing many amino acid units, each joined to the next by a peptide bond

  • secondary structure

    The manner in which a protein is coiled or stretched. (Section 24.7)

  • SN2

    A bimolecular nucleophilic substitution reaction.

Textbook Survival Guides

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