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Solutions for Chapter 6.6: The Addition of an Alcohol to an Alkene

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9780321803221

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 6.6: The Addition of an Alcohol to an Alkene

Organic Chemistry was written by and is associated to the ISBN: 9780321803221. Chapter 6.6: The Addition of an Alcohol to an Alkene includes 4 full step-by-step solutions. Since 4 problems in chapter 6.6: The Addition of an Alcohol to an Alkene have been answered, more than 38128 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7.

Key Chemistry Terms and definitions covered in this textbook
  • autooxidation

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

  • Boyle’s law

    A law stating that at constant temperature, the product of the volume and pressure of a given amount of gas is a constant. (Section 10.3)

  • conjugate acid

    A substance formed by addition of a proton to a Brønsted–Lowry base. (Section 16.2)

  • coordination compound.

    A neutral species containing one or more complex ions. (23.3)

  • crystal field splitting (D).

    The energy difference between two sets of d orbitals in a metal atom when ligands are present. (23.5)

  • Dihedral angle

    The angle created by two intersecting planes.

  • dispersion forces

    Intermolecular forces resulting from attractions between induced dipoles. Also called London dispersion forces. (Section 11.2)

  • elastomer

    A material that can undergo a substantial change in shape via stretching, bending, or compression and return to its original shape upon release of the distorting force. (Section 12.6)

  • energy-level diagram

    A diagram that shows the energies of molecular orbitals relative to the atomic orbitals from which they are derived. Also called a molecular-orbital diagram. (Section 9.7)

  • Exothermic reaction

    A reaction in which the enthalpy of the products is lower than that of the reactants; a reaction in which heat is released.

  • Hemiacetal

    A molecule containing an !OH and an !OR or !OAr group bonded to the same carbon

  • intensive property

    A property that is independent of the amount of material considered, for example, density. (Section 1.3)

  • leaving group

    A group capable ofseparating from a compound.

  • Michael reaction

    A reaction in which a nucleophile attacks a conjugated p system, resulting in a 1,4-addition.

  • norbornane

    The common name for bicyclo[2.2.1]heptane.

  • nucleophilic aromatic substitution

    A substitution reaction in which an aromatic ring is attacked by a nucleophile, which replaces a leaving group.

  • polar aprotic solvent

    A solvent that lacks hydrogen atoms connected directly to an electronegative atom.

  • Polar covalent bond

    A covalent bond between atoms whose difference in electronegativity is between approximately 0.5 and 1.9.

  • Quaternary (4°) ammonium ion

    An ion in which nitrogen is bonded to four carbons and bears a positive charge

  • Wittig reaction

    A reaction that converts an aldehyde or ketone into an alkene, with the introduction of one or more carbon atoms.

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