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Solutions for Chapter 18: Ethers and Epoxides; Thiols and Sulfides

Organic Chemistry | 9th Edition | ISBN: 9781305080485 | Authors: John E. McMurry

Full solutions for Organic Chemistry | 9th Edition

ISBN: 9781305080485

Organic Chemistry | 9th Edition | ISBN: 9781305080485 | Authors: John E. McMurry

Solutions for Chapter 18: Ethers and Epoxides; Thiols and Sulfides

Solutions for Chapter 18
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Textbook: Organic Chemistry
Edition: 9
Author: John E. McMurry
ISBN: 9781305080485

This textbook survival guide was created for the textbook: Organic Chemistry, edition: 9. Since 76 problems in chapter 18: Ethers and Epoxides; Thiols and Sulfides have been answered, more than 56299 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by and is associated to the ISBN: 9781305080485. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 18: Ethers and Epoxides; Thiols and Sulfides includes 76 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • 1,2-adduct

    The product obtainedfrom 1,2-addition across a conjugated p system.

  • benzyne

    A high-energy intermediate formed during the elimination-addition reaction that occurs between chlorobenzene and either NaOH (at high temperature) or NaNH2.

  • Bile acid

    A cholesterol-derived detergent molecule, such as cholic acid, which is secreted by the gallbladder into the intestine to assist in the absorption of dietary lipids.

  • block copolymer

    A copolymer in which the different homopolymer subunits are connected together in one chain.

  • coordination compound

    A compound containing a metal ion bonded to a group of surrounding molecules or ions that act as ligands. (Section 23.2)

  • crown ether

    Cyclic polyethers whose molecular models resemble crowns.

  • Cyanohydrin

    A molecule containing an !OH group and a !CN group bonded to the same carbon.

  • dimensional analysis

    A method of problem solving in which units are carried through all calculations. Dimensional analysis ensures that the final answer of a calculation has the desired units. (Section 1.6)

  • double bond

    A covalent bond involving two electron pairs. (Section 8.3)

  • electromotive force (emf)

    A measure of the driving force, or electrical pressure, for the completion of an electrochemical reaction. Electromotive force is measured in volts: 1 V = 1 J>C. Also called the cell potential. (Section 20.4)

  • Freons

    CFCs that were heavily used for a wide variety of commercial applications, including as refrigerants, as propellants, in the production of foam insulation, as fire-fighting materials, and many other useful applications.

  • halohydrin formation

    A reaction which involves the addition of a halogen and a hydroxyl group (OH) across an alkene.

  • homopolymer

    A polymer constructed from a single type of monomer.

  • 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)

  • monomers

    Molecules with low molecular weights, which can be joined together (polymerized) to form a polymer. (Section 12.8)

  • N terminus

    For a peptide chain,the end that contains the amino group.

  • nitration

    An electrophilic aromatic substitution reaction that involves the installation of a nitro group (NO2) on an aromatic ring.

  • Pericyclic reaction

    A reaction that takes place in a single step, without intermediates, and involves a cyclic redistribution of bonding electrons

  • pressure–volume (PV) work

    Work performed by expansion of a gas against a resisting pressure. (Section 5.3)

  • Synstereoselective

    The addition of atoms or groups of atoms to the same face of a carbon-carbon double bond.

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