Solutions for Chapter 5.9: Dehydration of Alcohols

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 5.9: Dehydration of Alcohols

Solutions for Chapter 5.9
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Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Chapter 5.9: Dehydration of Alcohols includes 1 full step-by-step solutions. Since 1 problems in chapter 5.9: Dehydration of Alcohols have been answered, more than 12684 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • aldaric acid

    A dicarboxylic acid that is produced when an aldose or ketose is treated with a strong oxidizing agent, such as HNO3.

  • Atactic polymer

    A polymer with completely random confi gurations at the chiral centers along its chain, as, for example, atactic polypropylene

  • Cis, trans isomers

    Stereoisomers that have the same connectivity but a different arrangement of their atoms in space as a result of the presence of either a ring or a carboncarbon double bond.

  • Disulfide

    A molecule containing an !S!S! group

  • enthalpy

    A measure of the exchange of energy between the system and its surroundings during any process.

  • enthalpy of reaction

    The enthalpy change associated with a chemical reaction. (Section 5.4)

  • ferromagnetism

    A form of magnetism in which unpaired electron spins align parallel to one another. (Section 23.1)

  • Fishhook arrow

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

  • formal charge

    The number of valence electrons in an isolated atom minus the number of electrons assigned to the atom in the Lewis structure. (Section 8.5)

  • Haloform

    A compound of the type CHX3 where X is a halogen.

  • Hückel criteria for aromaticity

    To be aromatic, a monocyclic compound must have one 2p orbital on each atom of the ring, be planar or nearly so, and have (4n 1 2) p electrons in the cyclic arrangement of 2p orbitals

  • intermetallic compound

    A homogeneous alloy with definite properties and a fixed composition. Intermetallic compounds are stoichiometric compounds that form between metallic elements. (Section 12.3)

  • ionic compound

    A compound composed of cations and anions. (Section 2.7)

  • molecular equation

    A chemical equation in which the formula for each substance is written without regard for whether it is an electrolyte or a nonelectrolyte. (Section 4.2)

  • organohalide

    An organic compound containing at least one halogen.

  • particle accelerator

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

  • phenyl group

    A C6H5 group.

  • polyatomic ion

    An electrically charged group of two or more atoms. (Section 2.7)

  • Reducing sugar

    A carbohydrate that reacts with an oxidizing agent to form an aldonic acid. In this reaction, the carbohydrate reduces the oxidizing agent.

  • Schiemann reaction

    The conversion of an aryl diazonium salt into fluorobenzene upon treatment with fluoroboric acid (HBF4).

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