Solutions for Chapter 16.9: Preparation of Epoxides

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 16.9: Preparation of Epoxides

Solutions for Chapter 16.9
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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. Chapter 16.9: Preparation of Epoxides includes 1 full step-by-step solutions. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. Since 1 problems in chapter 16.9: Preparation of Epoxides have been answered, more than 10970 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • amalgam.

    An alloy of mercury with another metal or metals. (21.2)

  • Annulene

    A cyclic hydrocarbon with a continuous alternation of single and double bonds.

  • diastereomers

    Stereoisomers that are not mirror images of one another.

  • E

    For alkenes, a stereodescriptorthat indicates that the two priority groups are on opposite sides of the p bond.

  • elastomer

    A material that can undergo a substantial change in shape via stretching, bending, or compression and return to its original shape upon release of the distorting force. (Section 12.6)

  • Formal charge

    The charge on an atom in a polyatomic ion or molecule

  • fossil fuels

    Coal, oil, and natural gas, which are presently our major sources of energy. (Section 5.8)

  • Ground state

    The lowest energy state of a system.

  • heterogeneous catalyst

    A catalyst that does not dissolve in the reaction medium.

  • hydrocracking

    A process performed in the presence of hydrogen gas by which large alkanes in petroleum are converted into smaller alkanes that are more suitable for use as gasoline.

  • malonic ester synthesis

    Asynthetic technique that enables the transformationof a halide into a carboxylic acid with theintroduction of two new carbon atoms.

  • Newman projection

    A drawing style that is designed to show the conformation of a molecule.

  • proton transfer

    One of the four arrow-pushing patterns for ionic reactions.

  • Pyranose

    A six-membered cyclic form of a monosaccharide.

  • quaternary ammonium salt

    An ionic compound containing a positively charged nitrogen atom connected to four alkyl groups.

  • racemic mixture

    A mixture of equal amounts of the dextrorotatory and levorotatory forms of a chiral molecule. A racemic mixture will not rotate the plane of polarized light. (Section 23.4)

  • Retrosynthesis

    A process of reasoning backwards from a target molecule to a suitable set of starting materials.

  • Ring current

    An applied magnetic fi eld causes the p electrons of an aromatic ring to circulate, giving rise to the so-called ring current and an associated magnetic fi eld that opposes the applied fi eld in the middle of the ring but reinforces the applied fi eld on the outside of the ring.

  • silicates

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

  • thiols

    Compounds containing a mercapto group (SH).

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