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Solutions for Chapter 16.12: Acid-Catalyzed Ring Opening of 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 16.12: Acid-Catalyzed Ring Opening of Epoxides

Solutions for Chapter 16.12
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Chapter 16.12: Acid-Catalyzed Ring Opening of Epoxides includes 2 full step-by-step solutions. Since 2 problems in chapter 16.12: Acid-Catalyzed Ring Opening of Epoxides have been answered, more than 7538 students have viewed full step-by-step solutions from this chapter. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • aliphatic hydrocarbons.

    Hydrocarbons that do not contain the benzene group or the benzene ring. (24.1)

  • asymmetric hydrogenation

    The addition of H2 across only one face of a p bond.

  • atmospheric pressure.

    The pressure exerted by Earth’s atmosphere. (5.2)

  • autoionization

    The process whereby water spontaneously forms low concentrations of H+1aq2 and OH-1aq2 ions by proton transfer from one water molecule to another. (Section 16.3)

  • copolymer

    A complex polymer resulting from the polymerization of two or more chemically different monomers. (Section 12.8)

  • crossed aldol reaction

    An aldol reaction that occurs between different partners.

  • dynamic equilibrium

    A state of balance in which opposing processes occur at the same rate. (Section 11.5)

  • folding

    The process by which a protein adopts its biologically active shape. (Section 24.7)

  • hydrochlorofluorocarbons, (HCFCs)

    Compounds that are similar in structure to CFCs but also possess at least one C!Hbond.

  • isoelectric point (pI)

    For an amino acid, the specific pH at which the concentration of the zwitterionic form reaches its maximum value.

  • mass number

    The sum of the number of protons and neutrons in the nucleus of a particular atom. (Section 2.3)

  • mole fraction

    The ratio of the number of moles of one component of a mixture to the total moles of all components; abbreviated X, with a subscript to identify the component. (Section 10.6)

  • N-bromosuccinimide

    A reagent used for allylic bromination to avoid a competing reaction in which bromine adds across the p bond.

  • oxymercuration-demercuration

    A two-step process for the Markovnikov addition of water across an alkene. With this process, carbocation rearrangements do not occur.

  • ozonolysis

    A reaction in which the CRC bond of an alkene is cleaved to form two CRO bonds.

  • photon

    The smallest increment (a quantum) of radiant energy; a photon of light with frequency n has an energy equal to hn. (Section 6.2)

  • Stereospecific reaction

    A special type of stereoselective reaction in which the stereochemistry of the product is dependent on the stereochemistry of the starting material.

  • trivalent

    An element, such as nitrogen, that forms three bonds.

  • Wavelength (l)

    The distance between consecutive peaks on a wave

  • weak activators

    Groups that weakly activate an aromatic ring toward electrophilic aromatic substitution, thereby enhancing the rate of the reaction.

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