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Solutions for Chapter 15: Reactions of Aromatic Compounds

Organic Chemistry | 11th Edition | ISBN: 9781118133576 | Authors: T. W. Graham Solomons Craig B. Fryhle, Scott A. Snyder

Full solutions for Organic Chemistry | 11th Edition

ISBN: 9781118133576

Organic Chemistry | 11th Edition | ISBN: 9781118133576 | Authors: T. W. Graham Solomons Craig B. Fryhle, Scott A. Snyder

Solutions for Chapter 15: Reactions of Aromatic Compounds

Solutions for Chapter 15
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Textbook: Organic Chemistry
Edition: 11
Author: T. W. Graham Solomons Craig B. Fryhle, Scott A. Snyder
ISBN: 9781118133576

This expansive textbook survival guide covers the following chapters and their solutions. Since 53 problems in chapter 15: Reactions of Aromatic Compounds have been answered, more than 46561 students have viewed full step-by-step solutions from this chapter. Chapter 15: Reactions of Aromatic Compounds includes 53 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 11. Organic Chemistry was written by and is associated to the ISBN: 9781118133576.

Key Chemistry Terms and definitions covered in this textbook
  • acid-dissociation constant (Ka)

    An equilibrium constant that expresses the extent to which an acid transfers a proton to solvent water. (Section 16.6)

  • amplitude.

    The vertical distance from the middle of a wave to the peak or trough. (7.1)

  • aromatic

    A compound containing a planar ring of continuously overlapping p orbitals with 4n+2p electrons.

  • b-Pleated sheet

    A type of polypeptide secondary structure in which sections of polypeptide chains are aligned parallel or antiparallel to one another.

  • bidentate ligand

    A ligand in which two linked coordinating atoms are bound to a metal. (Section 23.3)

  • bond-line structures

    The most common drawing style employed by organic chemists. All carbon atoms and most hydrogen atoms are implied but not explicitly drawn in a bond-line structure.

  • boranes

    Covalent hydrides of boron. (Section 22.11)

  • Brønsted-Lowry acid

    A proton donor

  • cation

    A structure that bears a positive charge.

  • Celsius scale

    A temperature scale on which water freezes at 0° and boils at 100° at sea level. (Section 1.4)

  • heterolytic bond cleavage

    Bond breaking that results in the formation of ions.

  • lambda max (lmax)

    In UVVis spectroscopy, the wavelength of maximum absorption.

  • London dispersion forces

    Attractive forces between transient dipole moments, observed in alkanes.

  • metric system

    A system of measurement used in science and in most countries. The meter and the gram are examples of metric units. (Section 1.4)

  • molecular-orbital diagram

    A diagram that shows the energies of molecular orbitals relative to the atomic orbitals from which they are derived; also called an energy-level diagram. (Section 9.7)

  • particle accelerator

    A device that uses strong magnetic and electrostatic fields to accelerate charged particles. (Section 21.3)

  • Polyester

    A polymer in which each monomer unit is joined to the next by an ester bond, as, for example, poly(ethylene terephthalate).

  • Shell

    A region of space around a nucleus that can be occupied by electrons, corresponding to a principal quantum number

  • Steric strain

    The strain that arises when nonbonded atoms separated by four or more bonds are forced closer to each other than their atomic (contact) radii would allow. Steric strain is also called non-bonded interaction strain, or van der Waals strain.

  • valence bond theory

    A theory that treats a bond as the sharing of electrons that are associated with individual atoms, rather than being associated with the entire molecule.

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