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Solutions for Chapter 11.2: The Structure of Benzene

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 11.2: The Structure of Benzene

Solutions for Chapter 11.2
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This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Since 1 problems in chapter 11.2: The Structure of Benzene have been answered, more than 34228 students have viewed full step-by-step solutions from this chapter. Chapter 11.2: The Structure of Benzene includes 1 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Aglycon

    Lacking a sugar

  • amide

    An organic compound that has an NR2 group attached to a carbonyl. (Section 24.4)

  • antiaromatic

    Instability that arises when a planar ring of continuously overlapping p orbitals contains 4n p electrons.

  • Brønsted-Lowry base

    A proton acceptor

  • conjugate acid

    In an acid-base reaction, the product that results when a base is protonated.

  • coordination-sphere isomers

    Structural isomers of coordination compounds in which the ligands within the coordination sphere differ. (Section 23.4)

  • 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)

  • diborane

    B2H6. A dimeric structure formed when one borane molecule reacts with another.

  • electron domain

    In the VSEPR model, a region about a central atom in which an electron pair is concentrated. (Section 9.2)

  • extensive property

    A property that depends on the amount of material considered; for example, mass or volume. (Section 1.3)

  • frontier orbitals

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

  • Hydrogenolysis

    Cleavage of a single bond by H2, most commonly accomplished by treating a compound with H2 in the presence of a transition metal catalyst.

  • limiting reactant (limiting reagent)

    The reactant present in the smallest stoichiometric quantity in a mixture of reactants; the amount of product that can form is limited by the complete consumption of the limiting reactant. (Section 3.7)

  • living polymer

    A polymer that isformed via anionic polymerization.

  • meso compound

    A compound that possesses chirality centers and an internal plane of symmetry.

  • Nucleophilic aromatic substitution

    A reaction in which a nucleophile, most commonly a halogen, on an aromatic ring is replaced by another nucleophile.

  • organic chemistry

    The study of carbon-containing compounds, typically containing carbon–carbon bonds. (Section 2.9; Chapter 24:Introduction)

  • Polyunsaturated triglyceride

    A triglyceride having several carbon-carbon double bonds in the hydrocarbon chains of its three fatty acids.

  • s-trans

    A conformation of a conjugateddiene in which the disposition of the two p bonds with regard to the connecting single bond is translike (a dihedral angle of 180°).

  • sodium cyanoborohydride

    A selective reducing agent (NaBH3CN) that can be used for reductive amination.

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