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Solutions for Chapter 6.8: The Addition of Borane to an Alkene: HydroborationOxidation

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 8th Edition

ISBN: 9780134042282

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 6.8: The Addition of Borane to an Alkene: HydroborationOxidation

Solutions for Chapter 6.8
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This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by Patricia and is associated to the ISBN: 9780134042282. Since 2 problems in chapter 6.8: The Addition of Borane to an Alkene: HydroborationOxidation have been answered, more than 8510 students have viewed full step-by-step solutions from this chapter. Chapter 6.8: The Addition of Borane to an Alkene: HydroborationOxidation includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8.

Key Chemistry Terms and definitions covered in this textbook
  • (PAHs)

    Compounds containing multiple aromatic rings fused together.

  • Alkoxy group

    An !OR group where R is an alkyl group

  • amorphous

    A region of a polymer in which nearby chains are not linearly extended and are not parallel to one another.

  • atomic orbital.

    The wave function (?) of an electron in an atom. (7.5)

  • capillary action

    The process by which a liquid rises in a tube because of a combination of adhesion to the walls of the tube and cohesion between liquid particles. (Section 11.3)

  • Furanose

    A fi ve-membered cyclic form of a monosaccharide.

  • heat of vaporization

    The enthalpy change, ?H, for vaporization of a liquid. (Section 11.4)

  • Hückel criteria for aromaticity

    To be aromatic, a monocyclic compound must have one 2p orbital on each atom of the ring, be planar or nearly so, and have (4n 1 2) p electrons in the cyclic arrangement of 2p orbitals

  • Inductive effect

    The polarization of the electron density of a covalent bond caused by the electronegativity of a nearby atom.

  • localized lone pair

    A lone pair thatis not participating in resonance.

  • matter

    Anything that occupies space and has mass; the physical material of the universe. (Section 1.1)

  • Merrifield synthesis

    A method for building a peptide from protected building blocks.

  • molarity

    The concentration of a solution expressed as moles of solute per liter of solution; abbreviated M. (Section 4.5)

  • nuclear transmutation

    A conversion of one kind of nucleus to another. (Section 21.3)

  • Nucleophilic acyl substitution

    A reaction in which a nucleophile bonded to the carbon of an acyl group is replaced by another nucleophile.

  • oxaphosphetane

    An intermediate that is believed to be formed during Wittig reactions.

  • Pericyclic reaction

    A reaction that takes place in a single step, without intermediates, and involves a cyclic redistribution of bonding electrons

  • Pi (p) bond

    A covalent bond formed by the overlap of parallel 2p orbitals.

  • primitive lattice

    A crystal lattice in which the lattice points are located only at the corners of each unit cell. (Section 12.2)

  • symmetry forbidden

    A reaction that disobeys conservation of orbital symmetry.

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