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Solutions for Chapter 6.1: The Addition of a Hydrogen Halide 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 6.1: The Addition of a Hydrogen Halide to an Alkene

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. Chapter 6.1: The Addition of a Hydrogen Halide to an Alkene includes 3 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9780321803221. Since 3 problems in chapter 6.1: The Addition of a Hydrogen Halide to an Alkene have been answered, more than 42239 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • actinide element

    Element in which the 5f orbitals are only partially occupied. (Section 6.8)

  • bond cleavage

    The breaking of a bond, either homolytically or heterolytically. bond dissociation energy (Sect. 6.1): The energy required to achieve homolytic bond cleavage (generating radicals).

  • concentration of a solution.

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

  • desulfurization

    The conversion of a thioacetal into an alkane in the presence of Raney nickel.

  • diamagnetic anisotropy

    An effect that causes different regions of space to be characterized by different magnetic field strengths.

  • diffusion.

    The gradual mixing of molecules of one gas with the molecules of another by virtue of their kinetic properties. (5.7)

  • electromagnetic spectrum

    Therange of all frequencies of electromagnetic radiation,which is arbitrarily divided into severalregions, most commonly by wavelength.

  • energy of activation

    In an energy diagram, the height of the energy barrier (the hump) between the reactants and the products.

  • enzyme

    A protein molecule that acts to catalyze specific biochemical reactions. (Section 14.7)

  • ether

    A compound with the structure R!O!R.

  • free energy (Gibbs free energy, G)

    A thermodynamic state function that gives a criterion for spontaneous change in terms of enthalpy and entropy: G = H - TS. (Section 19.5)

  • heterogeneous alloy

    An alloy in which the components are not distributed uniformly; instead, two or more distinct phases with characteristic compositions are present. (Section 12.3)

  • Hofmann elimination

    When treated with a strong base, a quaternary ammonium halide undergoes b-elimination by an E2 mechanism to give the less-substituted alkene as the major product

  • Infrared active

    Any molecular vibration that leads to a substantial change in dipole moment and is observed in an IR spectrum.

  • lambda max (lmax)

    In UVVis spectroscopy, the wavelength of maximum absorption.

  • London dispersion forces

    Attractive forces between transient dipole moments, observed in alkanes.

  • nucleophile

    A compound containing an electron-rich atom that is capable of donating a pair of electrons.

  • probability density 1c22

    A value that represents the probability that an electron will be found at a given point in space. Also called electron density. (Section 6.5)

  • quantum mechanics

    A mathematical description of an electron that incorporates its wavelike properties.

  • tertiary alkyl halide

    An organohalide in which the alpha (a) position is connected to three alkyl groups.