Solutions for Chapter 5: Structure and Preparation of Alkenes: Elimination Reactions

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 5: Structure and Preparation of Alkenes: Elimination Reactions

Solutions for Chapter 5
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Textbook: Organic Chemistry,
Edition: 9
Author: Francis A Carey Dr., Robert M. Giuliano
ISBN: 9780073402741

Since 32 problems in chapter 5: Structure and Preparation of Alkenes: Elimination Reactions have been answered, more than 10707 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Chapter 5: Structure and Preparation of Alkenes: Elimination Reactions includes 32 full step-by-step solutions. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alkaloids

    Naturally occurring amines isolated from plants.

  • amino sugars

    Carbohydrate derivatives in which an OH group has been replaced with an amino group.

  • amorphous

    A region of a polymer in which nearby chains are not linearly extended and are not parallel to one another.

  • covalent bond.

    A bond in which two electrons are shared by two atoms. (9.4)

  • crystallite

    A region of a polymer inwhich the chains are linearly extended and closein proximity to one another, resulting in van der Waals forces that hold the chains close together.

  • dispersion forces

    Intermolecular forces resulting from attractions between induced dipoles. Also called London dispersion forces. (Section 11.2)

  • Fischer esterifi cation

    The process of forming an ester by refl uxing a carboxylic acid and an alcohol in the presence of an acid catalyst, commonly H2SO4, ArSO3H, or HCl

  • hybrid orbital

    An orbital that results from the mixing of different kinds of atomic orbitals on the same atom. For example, an sp3 hybrid results from the mixing, or hybridizing, of one s orbital and three p orbitals. (Section 9.5)

  • hydrophilic

    A polar group that has favorable interactions with water.

  • Lewis acid

    A compound capable offunctioning as an electron pair acceptor.

  • living polymer

    A polymer that isformed via anionic polymerization.

  • mass spectrometry

    The study ofthe interaction between matter and an energysource other than electromagnetic radiation. Massspectrometry is used primarily to determine the molecular weight and molecular formula of a compound.

  • matter waves

    The term used to describe the wave characteristics of a moving particle. (Section 6.4)

  • mercurinium ion

    The intermediateformed during oxymercuration.

  • metallurgy

    The science of extracting metals from their natural sources by a combination of chemical and physical processes. It is also concerned with the properties and structures of metals and alloys. (Section 23.1)

  • pi 1P2 bond

    A covalent bond in which electron density is concentrated above and below the internuclear axis. (Section 9.6)

  • polyprotic acid

    A substance capable of dissociating more than one proton in water; H2SO4 is an example. (Section 16.6)

  • positron emission

    A nuclear decay process where a positron, a particle with the same mass as an electron but with a positive charge, symbol 0+1e, or b+ is emitted from the nucleus. (Section 21.1)

  • Thermochemistry

    The study of the energy of chemical structures.

  • Z

    For alkenes, a stereodescriptor that indicates that the two priority groups are on the same side of the p bond.

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