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Solutions for Chapter 25: Organic Chemistry 8th Edition

Organic Chemistry | 8th Edition | ISBN: 9780321768414 | Authors: L.G. Wade Jr

Full solutions for Organic Chemistry | 8th Edition

ISBN: 9780321768414

Organic Chemistry | 8th Edition | ISBN: 9780321768414 | Authors: L.G. Wade Jr

Solutions for Chapter 25

Solutions for Chapter 25
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Textbook: Organic Chemistry
Edition: 8
Author: L.G. Wade Jr
ISBN: 9780321768414

Since 32 problems in chapter 25 have been answered, more than 206169 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 25 includes 32 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. Organic Chemistry was written by and is associated to the ISBN: 9780321768414.

Key Chemistry Terms and definitions covered in this textbook
  • 1,4-addition

    A reaction involving the addition of two groups to a conjugated p system in which one group is installed at the C1 position and the other group is installed at the C4 position.

  • accuracy.

    The closeness of a measurement to the true value of the quantity that is measured. (1.8)

  • activity series

    A list of metals in order of decreasing ease of oxidation. (Section 4.4)

  • alpha particles

    Particles that are identical to helium-4 nuclei, consisting of two protons and two neutrons, symbol 4 2He or 4 2a. (Section 21.1)

  • azo coupling

    An electrophilic aromatic substitution reaction in which an aryldiazonium salt reacts with an activated aromatic ring.

  • buffer solution.

    A solution of (a) a weak acid or base and (b) its salt; both components must be present. The solution has the ability to resist changes in pH upon the addition of small amounts of either acid or base. (16.3)

  • Chain-transfer reaction

    The transfer of reactivity of an endgroup from one chain to another during a polymerization

  • chemical bond

    A strong attractive force that exists between atoms in a molecule. (Section 8.1)

  • endo

    In Diels-Alder reactions that produce bicyclic structures, the positions that are syn to the larger bridge.

  • Fishhook arrow

    A barbed curved arrow used to show the change in position of a single electron.

  • heterogeneous catalyst

    A catalyst that does not dissolve in the reaction medium.

  • Mercaptan

    A common name for a thiol; that is, any compound that contains an -SH (sulfhydryl) group

  • miscible

    Two liquids that can be mixed with each other in any proportion.

  • polysaccharides

    Polymers made up of repeating monosaccharide units linked together by glycoside bonds.

  • random copolymer

    A polymer, comprised of more than one kind of repeating unit, in which there is a random distribution of repeating units.

  • Reducing sugar

    A carbohydrate that reacts with an oxidizing agent to form an aldonic acid. In this reaction, the carbohydrate reduces the oxidizing agent.

  • resonance structures (resonance forms)

    Individual Lewis structures in cases where two or more Lewis structures are equally good descriptions of a single molecule. The resonance structures in such an instance are “averaged” to give a more accurate description of the real molecule. (Section 8.6)

  • Valence electrons

    Electrons in the valence (outermost) shell of an atom.

  • wavelength

    The distance between adjacent peaks of an oscillating magnetic or electric field.

  • zwitterion

    A net neutral compound that exhibits charge separation. Amino acids exist as zwitterions at physiological pH.

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