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Solutions for Chapter 14.15SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Solutions for Chapter 14.15SE

Solutions for Chapter 14.15SE
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Since 2 problems in chapter 14.15SE have been answered, more than 261646 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. This expansive textbook survival guide covers the following chapters and their solutions. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Chapter 14.15SE includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • [4+2]-cycloaddition

    A pericyclic reaction, also called a Diels-Alder reaction, that takes place between two different p systems, one of which is associated with four atoms while the other is associated with two atoms.

  • alkene

    A compound that possesses a carbon-carbon double bond.

  • amine

    Compounds containing a nitrogen atom that is connected to one, two, or three alkyl or aryl groups.

  • amorphous solid.

    A solid that lacks a regular three-dimensional arrangement of atoms or molecules. (11.7)

  • Bond dipole moment

    A measure of the polarity of a covalent bond. The product of the charge on either atom of a polar bond times the distance between the atoms

  • Chiral center

    A tetrahedral atom, most commonly carbon, that is bonded to four different groups; also called a chirality center

  • Contributing structures

    Representations of a molecule or ion that differ only in the distribution of valence electrons.

  • decomposition reaction

    A chemical reaction in which a single compound reacts to give two or more products. (Section 3.2)

  • electrocyclic reaction

    A pericyclic process in which a conjugated polyene undergoes cyclization. In the process, one p bond is converted into a s bond, while the remaining p bonds all change their location. The newly formed s bond joins the ends of the original p system,thereby creating a ring.

  • Fluid-mosaic model

    A biological membrane that consists of a phospholipid bilayer with proteins, carbohydrates, and other lipids on the surface and embedded in the bilayer

  • fracking

    The practice in which water laden with sand and other materials is pumped at high pressure into rock formations to release natural gas and other petroleum materials. (Section 18.4)

  • free radical

    A substance with one or more unpaired electrons. (Section 21.9)

  • nucleophilic acyl substitution

    A reaction in which a nucleophile attacks a carboxylic acid derivative.

  • petroleum

    A naturally occurring combustible liquid composed of hundreds of hydrocarbons and other organic compounds. (Section 5.8)

  • Pi (p) molecular orbital

    A molecular orbital formed by overlapping parallel 2p orbitals on adjacent atoms; its electron density lies above and below the line connecting the atoms

  • regiochemistry

    A term describing a consideration that must be taken into account for a reaction in which two or more constitutional isomers can be formed.

  • retention time

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

  • reversible process

    A process that can go back and forth between states along exactly the same path; a system at equilibrium is reversible if equilibrium can be shifted by an infinitesimal modification of a variable such as temperature. (Section 19.1)

  • solvolysis

    A substitution reaction in which the solvent functions as the nucleophile.

  • Vicinal coupling

    a !CH"CH2 group

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