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Solutions for Chapter 8.2: nomenClature of alkyl HaliDes, alCoHols, tHiols, etHers, anD sulfiDes

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Full solutions for Organic Chemistry | 6th Edition

ISBN: 9781936221349

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Solutions for Chapter 8.2: nomenClature of alkyl HaliDes, alCoHols, tHiols, etHers, anD sulfiDes

Chapter 8.2: nomenClature of alkyl HaliDes, alCoHols, tHiols, etHers, anD sulfiDes includes 8 full step-by-step solutions. Since 8 problems in chapter 8.2: nomenClature of alkyl HaliDes, alCoHols, tHiols, etHers, anD sulfiDes have been answered, more than 33892 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: 6. Organic Chemistry was written by and is associated to the ISBN: 9781936221349.

Key Chemistry Terms and definitions covered in this textbook
  • alkoxymercuration-demercuration

    A two-step process that achieves Markovnikov addition of an alcohol (H and OR) across an alkene. The product of this process is an ether.

  • compound

    A substance composed of two or more elements united chemically in definite proportions. (Section 1.2)

  • Conjugate acid

    The species formed when a base accepts a proton from an acid

  • conjugate acid–base pair

    An acid and a base, such as H2O and OH-, that differ only in the presence or absence of a proton. (Section 16.2)

  • conjugated

    A compound in which two p bonds are separated from each other by exactly one s bond.

  • coupling (of radicals)

    A radical process in which two radicals join together and form a bond.

  • Enantiomers

    Stereoisomers that are nonsuperposable mirror images of each other; refers to a relationship between pairs of objects

  • hydrocracking

    A process performed in the presence of hydrogen gas by which large alkanes in petroleum are converted into smaller alkanes that are more suitable for use as gasoline.

  • instantaneous rate

    The reaction rate at a particular time as opposed to the average rate over an interval of time. (Section 14.2)

  • intermolecular forces

    The attractive forces between molecules.

  • labile

    Protons that are exchanged at a rapid rate.

  • LUMO

    The lowest unoccupied molecular orbital.

  • molecular-orbital theory

    A theory that accounts for the allowed states for electrons in molecules.(Section 9.7)

  • Phenyl group

    A group derived by removing an H from benzene; abbreviated C6H5! or Ph!.

  • primary cell

    A voltaic cell that cannot be recharged. (Section 20.7)

  • Retrosynthesis

    A process of reasoning backwards from a target molecule to a suitable set of starting materials.

  • Schiemann reaction

    The conversion of an aryl diazonium salt into fluorobenzene upon treatment with fluoroboric acid (HBF4).

  • sp-hybridized

    Atomic orbitals that are achieved by mathematically averaging one s orbital with only one p orbital to form two hybridized atomic orbitals.

  • Stereoselective reaction

    A reaction in which one stereoisomer is formed in preference to all others. A stereoselective reaction may be enantioselective or diastereoselective, as the case may be.

  • trigonal pyramidal

    A geometry adopted by an atom that has one lone pair and a steric number of 4.

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