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Solutions for Chapter 16.5: Preparation of Ethers

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 16.5: Preparation of Ethers

Solutions for Chapter 16.5
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Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. Chapter 16.5: Preparation of Ethers includes 1 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Since 1 problems in chapter 16.5: Preparation of Ethers have been answered, more than 25704 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • active site

    Specific site on a heterogeneous catalyst or an enzyme where catalysis occurs. (Section 14.7)

  • addition reaction.

    A reaction in which one molecule adds to another. (24.2)

  • amine

    A compound that has the general formula R3N, where R may be H or a hydrocarbon group. (Section 16.7)

  • Azeotrope

    A liquid mixture of constant composition with a boiling point that is different from that of any of its components.

  • concentration of a solution.

    The amount of solute present in a given quantity of solvent or solution. (4.5)

  • Enantiomeric excess (ee)

    The difference between the percentage of two enantiomers in a mixture

  • hexagonal close packing

    A crystal structure where the atoms are packed together as closely as possible. The close-packed layers adopt a two-layer repeating pattern, which leads to a primitive hexagonal unit cell. (Section 12.3)

  • Hydride ion

    A hydrogen atom with two electrons in its valence shell; H:!

  • ionic solids

    Solids that are composed of ions. (Section 12.1)

  • Meisenheimer complex

    Theresonance-stabilized intermediate of a nucleophilicaromatic substitution reaction.

  • metric system

    A system of measurement used in science and in most countries. The meter and the gram are examples of metric units. (Section 1.4)

  • N-glycoside

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

  • Optically active

    Refers to a compound that rotates the plane of plane-polarized light

  • phase change

    The conversion of a substance from one state of matter to another. The phase changes we consider are melting and freezing 1solid ? liquid2, sublimation and deposition, and vaporization and condensation 1liquid ? gas2. (Section 11.4)

  • pi (p) bond

    A bond formed from adjacent, overlapping p orbitals.

  • Planck constant (h)

    The constant that relates the energy and frequency of a photon, E = hn. Its value is 6.626 * 10-34 J@s. (Section 6.2)

  • polysaccharides

    Polymers made up of repeating monosaccharide units linked together by glycoside bonds.

  • pure substance

    Matter that has a fixed composition and distinct properties. (Section 1.2)

  • Synstereoselective

    The addition of atoms or groups of atoms to the same face of a carbon-carbon double bond.

  • 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.

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