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Solutions for Chapter 16.5SE: 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 16.5SE

Solutions for Chapter 16.5SE
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Chapter 16.5SE includes 2 full step-by-step solutions. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 16.5SE have been answered, more than 66596 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13.

Key Chemistry Terms and definitions covered in this textbook
  • alkanes

    Compounds of carbon and hydrogen containing only carbon–carbon single bonds. (Sections 2.9 and 24.2)

  • alkyl halide

    An organic compound containing at least one halogen.

  • alkylation

    A reaction that achieves the installation of an alkyl group. For example, an SN2 reaction in which an alkyl group is connected to an attacking nucleophile.

  • battery

    A self-contained electrochemical power source that contains one or more voltaic cells. (Section 20.7)

  • Boyle’s law

    A law stating that at constant temperature, the product of the volume and pressure of a given amount of gas is a constant. (Section 10.3)

  • condensation reaction

    A chemical reaction in which a small molecule (such as a molecule of water) is split out from between two reacting molecules. (Sections 12.6 and 22.8)

  • Conjugation

    A situation in which two multiple bonds are separated by a single bond. Alternatively, a series of overlapping 2p orbitals. 1,3-butadiene, for example, is a conjugated diene, and 3-butene-2-one is a conjugated enone

  • Crown ether

    A cyclic polyether derived from ethylene glycol and substituted ethylene glycols.

  • enzymes

    Important biological molecules that catalyze virtually all cellular processes.

  • Frost circle

    A graphic method for determining the relative energies of p MOs for planar, fully conjugated, monocyclic compounds.

  • haloform reaction

    A reaction in which a methyl ketone is converted into a carboxylic acid upon treatment with excess base and excess halogen, followed by aqueous acid.

  • HOMO

    The highest occupied molecular orbital.

  • Homolytic bond cleavage

    Cleavage of a bond so that each fragment retains one electron; formation of radicals.

  • migratory aptitude

    In a BaeyerVilliger oxidation, the migration rates of different groups, which determine the regiochemical outcome of the reaction.

  • N-glycoside

    The product obtained when a monosaccharide is treated with an amine in the presence of an acid catalyst.

  • peroxides

    Compounds with the general structure R!O!O!R.

  • plane of symmetry

    A plane that bisects a compound into two halves that are mirror images of each other.

  • Prostaglandin

    A member of the family of compounds having the 20-carbon skeleton of prostanoic acid

  • resonance stabilization

    The stabilization associated with the delocalization of electrons via resonance.

  • solution

    A mixture of substances that has a uniform composition; a homogeneous mixture. (Section 1.2)

Textbook Survival Guides

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