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Solutions for Chapter 29: Organic Chemistry 6th Edition

Organic Chemistry | 6th Edition | ISBN: 9780840054982 | Authors: William H. Brown, Christopher S. Foote , Brent L. Iverson, Eric Anslyn

Full solutions for Organic Chemistry | 6th Edition

ISBN: 9780840054982

Organic Chemistry | 6th Edition | ISBN: 9780840054982 | Authors: William H. Brown, Christopher S. Foote , Brent L. Iverson, Eric Anslyn

Solutions for Chapter 29

Solutions for Chapter 29
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Textbook: Organic Chemistry
Edition: 6
Author: William H. Brown, Christopher S. Foote , Brent L. Iverson, Eric Anslyn
ISBN: 9780840054982

This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by and is associated to the ISBN: 9780840054982. Chapter 29 includes 35 full step-by-step solutions. Since 35 problems in chapter 29 have been answered, more than 40135 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6.

Key Chemistry Terms and definitions covered in this textbook
  • (PAHs)

    Compounds containing multiple aromatic rings fused together.

  • aliphatic hydrocarbons.

    Hydrocarbons that do not contain the benzene group or the benzene ring. (24.1)

  • Benzylic position

    An sp3 -hybridized carbon bonded to a benzene ring

  • beta elimination

    An elimination reaction in which a proton from the beta (b) position is removed together with the leaving group, forming a double bond.

  • Bimolecular reaction

    A reaction in which two species are involved in the rate-determining step.

  • breeder reactor.

    A nuclear reactor that produces more fissionable materials than it uses. (19.5)

  • cephalins

    Phosphoglycerides that contain ethanolamine.

  • conductor.

    Substance capable of conducting electric current. (21.3)

  • coordinate covalent bond.

    A bond in which the pair of electrons is supplied by one of the two bonded atoms; also called a dative bond. (9.9)

  • crystal lattice

    An imaginary network of points on which the repeating motif of a solid may be imagined to be laid down so that the structure of the crystal is obtained. The motif may be a single atom or a group of atoms. Each lattice point represents an identical environment in the crystal. (Section 12.2)

  • d sugar

    A carbohydrate for whichthe chirality center farthest from the carbonylgroup will have an OH group pointing to theright in the Fischer projection.

  • Enol

    A compound containing a hydroxyl group bonded to a doubly bonded carbon atom.

  • frontier orbitals

    The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) that participate in a reaction.

  • homogeneous catalyst

    A catalyst that is in the same phase as the reactant substances. (Section 14.7)

  • nuclear magnetic resonance (NMR)

    A form of spectroscopy that involves the study of the interaction between electromagnetic radiation and the nuclei of atoms.

  • Nucleophilicity

    A kinetic property measured by the rate at which a nucleophile causes nucleophilic substitution on a reference compound under a standardized set of experimental conditions.

  • Restriction endonuclease

    An enzyme that catalyzes the hydrolysis of a particular phosphodiester bond within a DNA strand.

  • saturated

    A compound that contains no p bonds.

  • tetravalent

    An element, such as carbon, that forms four bonds.

  • vinylic carbocation

    A carbocation in which the positive charge resides on a vinylic carbon atom. This type of carbocation is very unstable and will not readily form in most cases.

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