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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 25694 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 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
  • Addition reaction

    A reaction in which two atoms or groups of atoms react with a double bond, forming a compound with the two new groups bonded to the carbons of the original double bond.

  • auxochrome

    When applying Woodward-Fieser rules, the groups attached to the chromophore.

  • bond length

    The distance between the centers of two bonded atoms. (Section 8.3)

  • crystal-field theory

    A theory that accounts for the colors and the magnetic and other properties of transition-metal complexes in terms of the splitting of the energies of metal ion d orbitals by the electrostatic interaction with the ligands. (Section 23.6)

  • diagonal relationship.

    Similarities between pairs of elements in different groups and periods of the periodic table. (8.6)

  • electron impact ionization (EI)

    In mass spectrometry, an ionization technique that involves bombarding a compoundwith high-energy electrons.

  • electron-domain geometry

    The three- dimensional arrangement of the electron domains around an atom according to the VSEPR model. (Section 9.2)

  • Enamine

    An unsaturated compound derived by the reaction of an aldehyde or ketone and a secondary amine followed by loss of H2O; R2C"CR!NR2

  • Energy

    The ability to do work.

  • High-resolution mass spectrometry

    Instrumentation that is capable of separating ions that differ in mass by as little as 0.0001 amu

  • Lindlar catalyst

    Finely powdered palladium metal deposited on solid calcium carbonate that has been specially modifi ed with lead salts. Its particular use is as a catalyst for the reduction of an alkyne to a cis alkene

  • lipid

    Naturally occurring compoundsthat can be extracted from cells usingnonpolar organic solvents.

  • metallic solids

    Solids that are composed of metal atoms. (Section 12.1)

  • phenoxide

    The conjugate base of phenol or a substituted phenol.

  • polarimeter

    A device that measures the rotation of plane-polarized light caused by optically active compounds.

  • Polysaccharide

    A carbohydrate containing a large number of monosaccharide units, each joined to the next by one or more glycosidic bonds.

  • silicates

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

  • standard emf, also called the standard cell potential 1E°2

    The emf of a cell when all reagents are at standard conditions. (Section 20.4)

  • steroids

    Lipids that are based on a tetracyclic ring system involving three six-membered rings and one five-membered ring. Cholesterol is an example.

  • torsional strain

    The difference in energy between staggered and eclipsed conformations (for example, in ethane).

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