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Solutions for Chapter 6.14: Regioselective, Stereoselective, and Stereospecific Reactions

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9780321803221

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 6.14: Regioselective, Stereoselective, and Stereospecific Reactions

Solutions for Chapter 6.14
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Chapter 6.14: Regioselective, Stereoselective, and Stereospecific Reactions includes 1 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9780321803221. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Since 1 problems in chapter 6.14: Regioselective, Stereoselective, and Stereospecific Reactions have been answered, more than 41522 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Absolute confi guration

    Which of the two possible isomers an enantiomer is (i.e., whether it is the right- or left-handed isomer).

  • alpha (a) amino acid

    A compound containing a carboxylic acid group (COOH) as well as an amino group (NH2), both of which are attached to the same carbon atom.

  • anode.

    The electrode at which oxidation occurs. (18.2)

  • chain branching

    During polymerization, the growth of a branch connected to the main chain.

  • critical pressure (Pc).

    The minimum pressure necessary to bring about liquefaction at the critical temperature. (11.8)

  • elemental semiconductor

    A semiconducting material composed of just one element. (Section 12.7)

  • extensive property

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

  • heterogeneous alloy

    An alloy in which the components are not distributed uniformly; instead, two or more distinct phases with characteristic compositions are present. (Section 12.3)

  • heterogeneous equilibrium

    The equilibrium established between substances in two or more different phases, for example, between a gas and a solid or between a solid and a liquid. (Section 15.4)

  • hydroboration-oxidation

    A twostep process that achieves an anti-Markovnikov addition of a proton and a hydroxyl group (OH) across an alkene.

  • hydrofluorocarbons (HFCs)

    Compounds that contain only carbon, fluorine, and hydrogen (no chlorine).

  • Hückel’s rule

    The requirement for an odd number of p electron pairs in order for a compound to be aromatic.

  • lattice energy

    The energy required to separate completely the ions in an ionic solid. (Section 8.2)

  • linkage isomers

    Structural isomers of coordination compounds in which a ligand differs in its mode of attachment to a metal ion. (Section 23.4)

  • liquid crystal

    A substance that exhibits one or more partially ordered liquid phases above the melting point of the solid form. By contrast, in nonliquid crystalline substances the liquid phase that forms upon melting is completely unordered. (Section 11.7)

  • periodic table

    The arrangement of elements in order of increasing atomic number, with elements having similar properties placed in vertical columns. (Section 2.5)

  • primary

    A term used to indicate that exactly one alkyl group is attached directly to a particular position. For example, a primary carbocation has one alkyl group (not more) attached directly to the electrophilic carbon atom (C+).

  • Resonance energy

    The difference in energy between a resonance hybrid and the most stable of its hypothetical contributing structures in which electrons are localized on particular atoms and in particular bonds.

  • SN1 reaction

    A unimolecular nucleophilic substitution reaction.

  • sulfonation

    An electrophilic aromatic substitution reaction in which an SO3H group is installed on an aromatic ring.

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