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Solutions for Chapter 8.16: Delocalized Electrons Can Affect the Product of a Reaction

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 8.16: Delocalized Electrons Can Affect the Product of a Reaction

Solutions for Chapter 8.16
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Organic Chemistry was written by Patricia and is associated to the ISBN: 9780321803221. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Since 2 problems in chapter 8.16: Delocalized Electrons Can Affect the Product of a Reaction have been answered, more than 8433 students have viewed full step-by-step solutions from this chapter. Chapter 8.16: Delocalized Electrons Can Affect the Product of a Reaction includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alkoxymercuration-demercuration

    A two-step process that achieves Markovnikov addition of an alcohol (H and OR) across an alkene. The product of this process is an ether.

  • Alkyne

    An unsaturated hydrocarbon that contains one or more carbon-carbon triple bonds.

  • calcination

    The heating of an ore to bring about its decomposition and the elimination of a volatile product. For example, a carbonate ore might be calcined to drive off CO2. (Section 23.2)

  • conductor.

    Substance capable of conducting electric current. (21.3)

  • Cope rearrangement

    A [3,3] sigmatropic rearrangement in which all six atoms of the cyclic transition state are carbon atoms.

  • dihydroxylation

    A reaction characterized by the addition of two hydroxyl groups (OH) across an alkene.

  • linkage isomers

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

  • mass-to-charge ratio(m/z)

    Thedetermining factor by which ions are separatedfrom each other in mass spectrometry.

  • N terminus

    For a peptide chain,the end that contains the amino group.

  • off-resonance decoupling

    In NMR spectroscopy, a technique in which only the one-bond couplings are observed. CH3 groups appear as quartets, CH2 groups appear as triplets, CH groups appear as doublets, and quaternary carbon atoms appear as singlets.

  • plastic

    A material that can be formed into particular shapes by application of heat and pressure. (Section 12.8)

  • quantum

    The smallest increment of radiant energy that may be absorbed or emitted; the magnitude of radiant energy is hn. (Section 6.2)

  • radical

    A chemical entity with an unpaired electron.

  • radioactive decay chain

    A series of nuclear reactions that begins with an unstable nucleus and terminates with a stable one. Also called nuclear disintegration series. (Section 21.2)

  • rate equation

    An equation thatdescribes the relationship between the rate of a reactionand the concentration of reactants.

  • retention time

    The amount of time required for a compound to exit from a gas chromatograph.

  • saponification

    The base-catalyzed hydrolysis of an ester. This method is used to make soap.

  • solute

    A substance dissolved in a solvent to form a solution; it is normally the component of a solution present in the smaller amount. (Section 4.1)

  • step-growth polymers

    Polymers that are formed under conditions in which the individual monomers react with each other to form oligomers, which are then joined together to form polymers.

  • Steroid

    A plant or animal lipid having the characteristic tetracyclic ring structure of the steroid nucleus, namely three sixmembered rings and one fi ve-membered ring.

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