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Solutions for Chapter 14: Ethers and Epoxides; Thiols and Sulfides

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 14: Ethers and Epoxides; Thiols and Sulfides

Solutions for Chapter 14
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Textbook: Organic Chemistry, - Standalone Book
Edition: 2
Author: David R. Klein
ISBN: 9781118452288

This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry, - Standalone Book was written by and is associated to the ISBN: 9781118452288. Chapter 14: Ethers and Epoxides; Thiols and Sulfides includes 72 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, - Standalone Book, edition: 2. Since 72 problems in chapter 14: Ethers and Epoxides; Thiols and Sulfides have been answered, more than 65993 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • alditol

    The product obtained when the aldehyde group of an aldose is reduced.

  • alkanes

    Compounds of carbon and hydrogen containing only carbon–carbon single bonds. (Sections 2.9 and 24.2)

  • anode

    An electrode at which oxidation occurs. (Section 20.3)

  • anomeric carbon

    The C1 position of the cyclic hemiacetal of an aldose or the C2 position of the cyclic hemiacetal of a ketose.

  • beta emission

    A nuclear decay process where a beta particle is emitted from the nucleus; also called beta decay. (Section 21.1)

  • chemical reaction.

    A process in which a substance (or substances) is changed into one or more new substances. (3.7)

  • diagnostic region

    The region of an IR spectrum that contains signals that arise from double bonds, triple bonds, and X!H bonds.

  • Diamagnetic current in NMR

    The circulation of electron density in a molecule in an applied magnetic fi eld.

  • disulfide

    A compound with the structure R!S!S!R.

  • glycogen

    The general name given to a group of polysaccharides of glucose that are synthesized in mammals and used to store energy from carbohydrates. (Section 24.7)

  • halogen abstraction

    In radical reactions, a type of arrow-pushing pattern in which a halogen atom is abstracted by a radical, generating a new radical.

  • ion–dipole force

    The force that exists between an ion and a neutral polar molecule that possesses a permanent dipole moment. (Section 11.2)

  • IUPAC

    The International Union of Pure and Applied Chemistry

  • oxidation

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

  • Phasing

    The sign of the wave function at particular coordinates in space, either plus or minus. Phasing is often represented by colors, such as red or blue

  • phosphatidic acid

    A phosphoric monoester, which is the simplest kind of phosphoglyceride.

  • Reducing sugar

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

  • sigmatropic rearrangements

    A pericyclic reaction in which one s bond is formed at the expense of another.

  • silicates

    Compounds containing silicon and oxygen, structurally based on SiO4 tetrahedra. (Section 22.10)

  • waxes

    High-molecular-weight esters that are constructed from carboxylic acids and alcohols.

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