Solutions for Chapter 22: Organic Chemistry

Modern Chemistry: Student Edition 2012 | 1st Edition | ISBN: 9780547586632 | Authors: Jerry L. Sarquis, Mickey Sarquis

Full solutions for Modern Chemistry: Student Edition 2012 | 1st Edition

ISBN: 9780547586632

Modern Chemistry: Student Edition 2012 | 1st Edition | ISBN: 9780547586632 | Authors: Jerry L. Sarquis, Mickey Sarquis

Solutions for Chapter 22: Organic Chemistry

Solutions for Chapter 22
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Textbook: Modern Chemistry: Student Edition 2012
Edition: 1
Author: Jerry L. Sarquis, Mickey Sarquis
ISBN: 9780547586632

This expansive textbook survival guide covers the following chapters and their solutions. Chapter 22: Organic Chemistry includes 62 full step-by-step solutions. Modern Chemistry: Student Edition 2012 was written by Patricia and is associated to the ISBN: 9780547586632. Since 62 problems in chapter 22: Organic Chemistry have been answered, more than 22285 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Modern Chemistry: Student Edition 2012, edition: 1.

Key Chemistry Terms and definitions covered in this textbook
  • Acylation

    The process of introducing an acyl group, RCO! or ArCO!, onto an organic molecule.

  • alkali metals.

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

  • Carbocation

    A species in which a carbon atom has only six electrons in its valence shell and bears a positive charge

  • Correlation tables

    Tables of data on absorption patterns of functional groups.

  • decomposition reaction.

    The breakdown of a compound into two or more components. (4.4)

  • DEPT 13C NMR

    In 13C NMR spectroscopy, a technique that utilizes two rf radiation emitters and provides information regarding the number of protons attached to each carbon atom in a compound.

  • electrometallurgy

    The use of electrolysis to reduce or refine metals. (Section 20.9)

  • electrophile

    A compound containing an electron-deficient atom that is capable of accepting a pair of electrons.

  • enantiotopic

    Protons that are not interchangeable by rotational symmetry but are interchangeable by reflectional symmetry.

  • Fishhook arrow

    A barbed curved arrow used to show the change in position of a single electron.

  • folding

    The process by which a protein adopts its biologically active shape. (Section 24.7)

  • Friedel-Crafts reaction

    An electrophilic aromatic substitution in which a hydrogen of an aromatic ring is replaced by an alkyl or acyl group.

  • Hydrogenolysis

    Cleavage of a single bond by H2, most commonly accomplished by treating a compound with H2 in the presence of a transition metal catalyst.

  • indicator

    A substance added to a solution that changes color when the added solute has reacted with all the solute present in solution. The most common type of indicator is an acid–base indicator whose color changes as a function of pH. (Section 4.6)

  • N-bromosuccinimide

    A reagent used for allylic bromination to avoid a competing reaction in which bromine adds across the p bond.

  • Nernst equation

    An equation that relates the cell emf, E, to the standard emf, E°, and the reaction quotient, Q: E = E° - 1RT>nF2 ln Q. (Section 20.6)

  • Polarimeter

    An instrument for measuring the ability of a compound to rotate the plane of plane-polarized light.

  • quantum

    The smallest increment of radiant energy that may be absorbed or emitted; the magnitude of radiant energy is hn. (Section 6.2)

  • specific heat 1Cs2

    The heat capacity of 1 g of a substance; the heat required to raise the temperature of 1 g of a substance by 1 °C. (Section 5.5)

  • substitution reactions

    Reactions in which one group is replaced by another group.

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