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Solutions for Chapter 16.1: Nomenclature of Ethers, Epoxides, and Sulfides

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 16.1: Nomenclature of Ethers, Epoxides, and Sulfides

Solutions for Chapter 16.1
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Since 1 problems in chapter 16.1: Nomenclature of Ethers, Epoxides, and Sulfides have been answered, more than 36448 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 16.1: Nomenclature of Ethers, Epoxides, and Sulfides includes 1 full step-by-step solutions. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9.

Key Chemistry Terms and definitions covered in this textbook
  • Acylation

    The process of introducing an acyl group, RCO! or ArCO!, onto an organic molecule.

  • Allylic

    Next to a carbon-carbon double bond.

  • alpha (a) amino acid

    A compound containing a carboxylic acid group (COOH) as well as an amino group (NH2), both of which are attached to the same carbon atom.

  • Angle strain

    The strain that arises when a bond angle is either compressed or expanded compared to its optimal value.

  • autooxidation

    The slow oxidation of organic compounds that occurs in the presence of atmospheric oxygen.

  • basic oxide (basic anhydride)

    An oxide that either reacts with water to form a base or reacts with an acid to form a salt and water. (Section 22.5)

  • bond polarity

    A measure of the degree to which the electrons are shared unequally between two atoms in a chemical bond. (Section 8.4)

  • conservation of orbital symmetry

    During a reaction, the requirement that the phases of the frontier MOs must be aligned.

  • Contributing structures

    Representations of a molecule or ion that differ only in the distribution of valence electrons.

  • copolymer.

    A polymer containing two or more different monomers. (25.2)

  • d–d transition

    The transition of an electron in a transition-metal compound from a lower-energy d orbital to a higher-energy d orbital. (Section 23.6)

  • Edman degradatio

    A method for selectively cleaving and identifying the N-terminal amino acid of a polypeptide chain.

  • elimination-addition

    A reaction that occurs between chlorobenzene and either NaOH (at high temperature) or NaNH2.

  • 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)

  • physical changes

    Changes (such as a phase change) that occur with no change in chemical composition. (Section 1.3)

  • Rate determining step

    The step in a multistep reaction sequence that crosses the highest energy barrier.

  • reducing sugar

    A carbohydrate that is oxidized upon treatment with Tollens’ reagent, Fehling’s reagent, or Benedict’s reagent.

  • scientific law

    A concise verbal statement or a mathematical equation that summarizes a wide range of observations and experiences. (Section 1.3)

  • tosylate

    An excellent leaving group (OTs). transition state (Sect. 6.6): A state through which a reaction passes. On an energy diagram, a transition state corresponds with a local maximum.

  • wavelength

    The distance between adjacent peaks of an oscillating magnetic or electric field.

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