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Organic Chemistry 7th Edition - Solutions by Chapter

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

Organic Chemistry | 7th Edition - Solutions by Chapter

The full step-by-step solution to problem in Organic Chemistry were answered by Patricia, our top Chemistry solution expert on 03/16/18, 05:02PM. This expansive textbook survival guide covers the following chapters: 24. Organic Chemistry was written by Patricia and is associated to the ISBN: 9781133952848. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Since problems from 24 chapters in Organic Chemistry have been answered, more than 4006 students have viewed full step-by-step answer.

Key Chemistry Terms and definitions covered in this textbook
  • alkynes.

    Hydrocarbons that contain one or more carbon-carbon triple bonds. They have the general formula CnH2n22, where n 5 2,3, . . . . (24.2)

  • alpha decay

    A type of radioactive decay in which an atomic nucleus emits an alpha particle and thereby transforms (or “decays”) into an atom with a mass number 4 less and atomic number 2 less. (Section 21.1)

  • atomic radius.

    One-half the distance between the two nuclei in two adjacent atoms of the same element in a metal. For elements that exist as diatomic units, the atomic radius is one-half the distance between the nuclei of the two atoms in a particular molecule. (8.3)

  • beta particles

    Energetic electrons emitted from the nucleus, symbol 0-1e or b-. (Section 21.1)

  • bonding molecular orbital.

    A molecular orbital that is of lower energy and greater stability than the atomic orbitals from which it was formed. (10.6)

  • carbide

    A binary compound of carbon with a metal or metalloid. (Section 22.9)

  • Deactivating group

    Any substituent on a benzene ring that causes the rate of electrophilic aromatic substitution to be lower than that for benzene.

  • debye (D)

    A unit of measure fordipole moments, where 1 debye = 10-18 esu×cm.

  • electrophoresis

    A technique for separating amino acids from each other based on a difference in pI values.

  • energy of activation

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

  • enol

    A compound containing a hydroxyl group (OH) connected directly to a carbon-carbon double bond.

  • Ground-state electron confi guration

    The lowest-energy electron confi guration for an atom or molecule.

  • Heterolytic bond cleavage

    Cleavage of a bond so that one fragment retains both electrons and the other retains none.

  • nomenclature

    A system for naming organic compounds.

  • polar molecule

    A molecule that possesses a nonzero dipole moment. (Section 8.4)

  • qualitative analysis

    The determination of the presence or absence of a particular substance in a mixture. (Section 17.7)

  • radical anion

    An intermediate that has both a negative charge and an unpaired electron.

  • retention of configuration

    During a reaction, when the configuration of a chirality center remains unchanged.

  • retention time

    The amount of time required for a compound to exit from a gas chromatograph.

  • Stereospecific reaction

    A special type of stereoselective reaction in which the stereochemistry of the product is dependent on the stereochemistry of the starting material.

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