×
Log in to StudySoup
Get Full Access to Chemistry - Textbook Survival Guide
Join StudySoup for FREE
Get Full Access to Chemistry - Textbook Survival Guide

Solutions for Chapter 16: Ethers, Epoxides, and Sulfides

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 16: Ethers, Epoxides, and Sulfides

Solutions for Chapter 16
4 5 0 354 Reviews
31
0
Textbook: Organic Chemistry,
Edition: 9
Author: Francis A Carey Dr., Robert M. Giuliano
ISBN: 9780073402741

Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. Since 29 problems in chapter 16: Ethers, Epoxides, and Sulfides have been answered, more than 36553 students have viewed full step-by-step solutions from this chapter. Chapter 16: Ethers, Epoxides, and Sulfides includes 29 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9.

Key Chemistry Terms and definitions covered in this textbook
  • Alkyne

    An unsaturated hydrocarbon that contains one or more carbon-carbon triple bonds.

  • basic oxide (basic anhydride)

    An oxide that either reacts with water to form a base or reacts with an acid to form a salt and water. (Section 22.5)

  • chemical bond

    A strong attractive force that exists between atoms in a molecule. (Section 8.1)

  • fragmentation

    In mass spectrometry, when the molecular ion breaks apart into fragments.

  • 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.

  • half-life

    The time required for the concentration of a reactant substance to decrease to half its initial value; the time required for half of a sample of a particular radioisotope to decay. (Sections 14.4 and 21.4)

  • hydronium ion 1H3O+2

    The predominant form of the proton in aqueous solution. (Section 16.2)

  • Imide

    A functional group in which two acyl groups, RCO! or ArCO!, are bonded to a nitrogen atom

  • Lewis symbol (electron-dot symbol)

    The chemical symbol for an element, with a dot for each valence electron. (Section 8.1)

  • Organometallic compound

    A compound that contains a carbon-metal bond.

  • Oxidative addition

    Addition of a reagent to a metal center causing it to add two substituents and to increase its oxidation state by two

  • phospholipid

    A form of lipid molecule that contains charged phosphate groups. (Section 24.9)

  • polynucleotide

    A polymer constructed from nucleotides linked together.

  • Polyunsaturated triglyceride

    A triglyceride having several carbon-carbon double bonds in the hydrocarbon chains of its three fatty acids.

  • prostaglandins

    Lipids that contain 20 carbon atoms and are characterized by a five-membered ring with two side chains.

  • Quaternary (4°) ammonium ion

    An ion in which nitrogen is bonded to four carbons and bears a positive charge

  • spectroscopy

    The study of the interaction between matter and electromagnetic radiation.

  • Stereospecific reaction

    A special type of stereoselective reaction in which the stereochemistry of the product is dependent on the stereochemistry of the starting material.

  • sulfone

    A compound that contains a sulfur atom that has double bonds with two oxygen atoms and is flanked on both sides by R groups.

  • terminal alkynes

    Compounds with the following structure: R!C#C!H

×
Log in to StudySoup
Get Full Access to Chemistry - Textbook Survival Guide
Join StudySoup for FREE
Get Full Access to Chemistry - Textbook Survival Guide
×
Reset your password