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Solutions for Chapter 8: Haloalkanes, Halogenation, and Radical Reactions

Organic Chemistry | 7th Edition | ISBN: 9781133952848 | Authors: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9781133952848

Organic Chemistry | 7th Edition | ISBN: 9781133952848 | Authors: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Solutions for Chapter 8: Haloalkanes, Halogenation, and Radical Reactions

Solutions for Chapter 8
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Textbook: Organic Chemistry
Edition: 7
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
ISBN: 9781133952848

Chapter 8: Haloalkanes, Halogenation, and Radical Reactions includes 30 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by and is associated to the ISBN: 9781133952848. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Since 30 problems in chapter 8: Haloalkanes, Halogenation, and Radical Reactions have been answered, more than 56739 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • alkali metals.

    The Group 1A elements (Li, Na, K, Rb, Cs, and Fr). (2.4)

  • Chair conformation

    The most stable nonplanar conformation of a cyclohexane ring; all bond angles are approximately 109.5°, and all bonds on adjacent carbons are staggered.

  • degenerate

    A situation in which two or more orbitals have the same energy. (Section 6.7)

  • electron shell

    A collection of orbitals that have the same value of n. For example, the orbitals with n = 3 (the 3s, 3p, and 3d orbitals) comprise the third shell. (Section 6.5)

  • Electrophilic aromatic substitution

    A reaction in which there is substitution of an electrophile, E1, for a hydrogen on an aromatic ring

  • Hell-Volhard-Zelinsky reaction

    A reaction in which a carboxylic acid undergoes a-halogenation when treated with bromine in the presence of PBr3.

  • Hess’s law

    The heat evolved in a given process can be expressed as the sum of the heats of several processes that, when added, yield the process of interest. (Section 5.6)

  • intermetallic compound

    A homogeneous alloy with definite properties and a fixed composition. Intermetallic compounds are stoichiometric compounds that form between metallic elements. (Section 12.3)

  • matter

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

  • observed rotation

    The extent to which plane-polarized light is rotated by a solution of a chiral compound.

  • oxidation

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

  • peptide

    A chain comprised of a small number of amino acid residues.

  • phosphoglycerides

    Compounds that are very similar in structure to triglycerides, with the main difference being that one of the three fatty acid residues is replaced by a phosphoester group.

  • reducing sugar

    A carbohydrate that is oxidized upon treatment with Tollens’ reagent, Fehling’s reagent, or Benedict’s reagent.

  • Solvolysis

    A nucleophilic substitution in which the solvent is also the nucleophile

  • specific rotation

    For a chiral compound that is subjected to plane-polarized light, the observed rotation when a standard concentration (1 g/mL) and a standard path length (1 dm) are used.

  • Steric hindrance

    The ability of groups, because of their size, to hinder access to a reaction site within a molecule.

  • sulfide

    A compound that is similar in structure to an ether, but the oxygen atom has been replaced with a sulfur atom. Also called a thioether.

  • tertiary alkyl halide

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

  • wedge

    In bond-line structures, a group in front of the page.