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Solutions for Chapter 17: Conjugated Pi Systems and Pericyclic Reactions

Organic Chemistry,  - Standalone Book | 2nd Edition | ISBN: 9781118452288 | Authors: David R. Klein

Full solutions for Organic Chemistry, - Standalone Book | 2nd Edition

ISBN: 9781118452288

Organic Chemistry,  - Standalone Book | 2nd Edition | ISBN: 9781118452288 | Authors: David R. Klein

Solutions for Chapter 17: Conjugated Pi Systems and Pericyclic Reactions

Solutions for Chapter 17
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Textbook: Organic Chemistry, - Standalone Book
Edition: 2
Author: David R. Klein
ISBN: 9781118452288

Since 79 problems in chapter 17: Conjugated Pi Systems and Pericyclic Reactions have been answered, more than 15218 students have viewed full step-by-step solutions from this chapter. Organic Chemistry, - Standalone Book was written by Patricia and is associated to the ISBN: 9781118452288. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 17: Conjugated Pi Systems and Pericyclic Reactions includes 79 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, - Standalone Book, edition: 2.

Key Chemistry Terms and definitions covered in this textbook
  • Activation energy

    The difference in Gibbs free energy between reactants and a transition state

  • addition reaction

    A reaction in which a reagent adds to the two carbon atoms of a carbon–carbon multiple bond. (Section 24.3)

  • carbonyl group

    The C “O double bond, a characteristic feature of several organic functional groups, such as ketones and aldehydes. (Section 24.4)

  • cation.

    An ion with a net positive charge. (2.5)

  • chemical energy.

    Energy stored within the structural units of chemical substances. (6.1)

  • chemistry.

    The study of matter and the changes it undergoes. (1.1)

  • crystallite

    A region of a polymer inwhich the chains are linearly extended and closein proximity to one another, resulting in van der Waals forces that hold the chains close together.

  • Disproportionation

    A termination process that involves the abstraction of a hydrogen atom from the beta position of the propagating radical of one chain by the radical endgroup of another chain.

  • electron-sea model

    A model for the behavior of electrons in metals. (Section 12.4)

  • energy of activation

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

  • Enthalpy change, DH

    The difference in total bond strengths and solvation between various points under comparison on a reaction coordinate diagram

  • enthalpy of formation

    The enthalpy change that accompanies the formation of a substance from the most stable forms of its component elements. (Section 5.7)

  • nuclear transmutation

    A conversion of one kind of nucleus to another. (Section 21.3)

  • Oxonium ion

    An ion in which oxygen bears a positive charge.

  • Polyurethane

    A polymer containing the !NHCO2! group as a repeating unit

  • reduction

    A process in which a substance gains one or more electrons. (Section 4.4)

  • secondary

    A term used to indicate that exactly two alkyl groups are attached directly to a particular position. For example, a secondary carbocation has two alkyl groups attached directly to the electrophilic carbon atom (C+).

  • tetravalent

    An element, such as carbon, that forms four bonds.

  • Transesterifi cation

    Exchange of the !OR or !OAr group of an ester for another !OR or !OAr group.

  • trigonal pyramidal

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

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