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Solutions for Chapter 15.4: Preparation of Alcohols from Epoxides

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 15.4: Preparation of Alcohols from Epoxides

Solutions for Chapter 15.4
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Chapter 15.4: Preparation of Alcohols from Epoxides includes 1 full step-by-step solutions. Since 1 problems in chapter 15.4: Preparation of Alcohols from Epoxides have been answered, more than 18186 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their 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
  • addition reactions

    Reactions that are characterized by the addition of two groups across a double bond. In the process, the pi (p) bond is broken.

  • alkane

    A hydrocarbon that lacks p bonds.

  • basic anhydride (basic oxide)

    An oxide that forms a base when added to water; soluble metal oxides are basic anhydrides. (Section 22.5)

  • carbides.

    Ionic compounds containing the C2 22 or C42 ion. (22.3)

  • double helix

    The structure for DNA that involves the winding of two DNA polynucleotide chains together in a helical arrangement. The two strands of the double helix are complementary in that the organic bases on the two strands are paired for optimal hydrogen bond interaction. (Section 24.10)

  • E2

    A bimolecular b-elimination reaction.

  • Electrophile

    From the Greek meaning electron loving. Any species that can accept a pair of electrons to form a new covalent bond; alternatively, a Lewis acid.

  • fibers

    Strands of a polymer that are generated when the polymer is heated, forced through small holes, and then cooled.

  • Haloform

    A compound of the type CHX3 where X is a halogen.

  • Hydrophilic

    From the Greek, meaning water-loving.

  • 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)

  • oxidation

    A reaction in which one compound undergoes an increase in oxidation state.

  • Polyester

    A polymer in which each monomer unit is joined to the next by an ester bond, as, for example, poly(ethylene terephthalate).

  • Sandmeyer reactions

    Reactions that utilize copper salts (CuX) and enable the installation of a halogen or a cyano group on an aromatic ring.

  • semiconductor

    A material that has electrical conductivity between that of a metal and that of an insulator. (Section 12.7)

  • step-growth polymers

    Polymers that are formed under conditions in which the individual monomers react with each other to form oligomers, which are then joined together to form polymers.

  • strong deactivators

    Groups that strongy deactivate an aromatic ring toward electrophilic aromatic substitution, thereby significantly decreasing the rate of the reaction.

  • Thermodynamic control

    Experimental conditions that permit the establishment of equilibrium between two or more products of a reaction. The composition of the product mixture is determined by the relative stabilities of the products.

  • 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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