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Solutions for Chapter 10.5SE: 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 10.5SE

Solutions for Chapter 10.5SE
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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. Since 2 problems in chapter 10.5SE have been answered, more than 67668 students have viewed full step-by-step solutions from this chapter. Chapter 10.5SE includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • acid ionization constant (Ka).

    The equilibrium constant for the acid ionization. (15.5)

  • alkaline earth metals

    Members of group 2A in the periodic table. (Section 7.7)

  • alkenes

    Hydrocarbons containing one or more carbon–carbon double bonds. (Section 24.2)

  • Alkyne

    An unsaturated hydrocarbon that contains one or more carbon-carbon triple bonds.

  • Beer’s law

    In UV-Vis spectroscopy, an equation describing the relationship between molar absorptivity (e), absorbance (A), concentration (C), and path length (l): e = A (C Ž l)

  • beta (b) position

    The position immediately adjacent to an alpha (a) position.

  • C terminus

    For a peptide chain,the end that contains the COOH group. carbinolamine (Sect. 20.6): A compound containing a hydroxyl group (OH) and a nitrogen atom, both of which are connceted to the same carbon atom.

  • carbonyl group

    The C “O double bond, a characteristic feature of several organic functional groups, such as ketones and aldehydes. (Section 24.4)

  • Charles’ and Gay-Lussac’s law.

    See Charles’ law.

  • Hund’s rule

    A rule stating that electrons occupy degenerate orbitals in such a way as to maximize the number of electrons with the same spin. In other words, each orbital has one electron placed in it before pairing of electrons in orbitals occurs. (Section 6.8)

  • inversion of configuration

    During a reaction, when the configuration of a chirality center is changed.

  • LUMO

    The lowest unoccupied molecular orbital.

  • molecular solids

    Solids that are composed of molecules. (Sections 12.1 and 12.6)

  • nitronium ion

    The NO2+ ion, which is present in a mixture of nitric acid and sulfuric acid.

  • Nucleotide

    A nucleoside in which a molecule of phosphoric acid is esterifi ed with an !OH of the monosaccharide, most commonly either the 39!OH or the 59!OH.

  • Orthogonal

    Having no net overlap.

  • radical initiator

    A compound with a weak bond that undergoes homolytic bond cleavage with great ease, producing radicals that can initiate a radical chain process.

  • Ring current

    An applied magnetic fi eld causes the p electrons of an aromatic ring to circulate, giving rise to the so-called ring current and an associated magnetic fi eld that opposes the applied fi eld in the middle of the ring but reinforces the applied fi eld on the outside of the ring.

  • solute

    A substance dissolved in a solvent to form a solution; it is normally the component of a solution present in the smaller amount. (Section 4.1)

  • thiolate

    The conjugate base of a thiol.

Textbook Survival Guides

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