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Solutions for Chapter 11: General Chemistry: Principles and Modern Applications 10th Edition

General Chemistry: Principles and Modern Applications | 10th Edition | ISBN: 9780132064521 | Authors: Ralph Petrucci

Full solutions for General Chemistry: Principles and Modern Applications | 10th Edition

ISBN: 9780132064521

General Chemistry: Principles and Modern Applications | 10th Edition | ISBN: 9780132064521 | Authors: Ralph Petrucci

Solutions for Chapter 11

Solutions for Chapter 11
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Textbook: General Chemistry: Principles and Modern Applications
Edition: 10
Author: Ralph Petrucci
ISBN: 9780132064521

Since 108 problems in chapter 11 have been answered, more than 46805 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: General Chemistry: Principles and Modern Applications, edition: 10. Chapter 11 includes 108 full step-by-step solutions. General Chemistry: Principles and Modern Applications was written by and is associated to the ISBN: 9780132064521.

Key Chemistry Terms and definitions covered in this textbook
  • anode

    An electrode at which oxidation occurs. (Section 20.3)

  • anti-Markovnikov addition

    An addition reaction in which a hydrogen atom is installed at the more substituted vinylic position and another group (such as a halogen) is installed at the less substituted vinylic position.

  • Aryl group (Ar -)

    A group derived from an arene by removal of an H.

  • Baeyer-Villiger oxidation

    A reaction in which a ketone is treated with a peroxy acid and is converted into an ester via the insertion of an oxygen atom.

  • bromonium ion

    A positively charged, bridged intermediate formed during the addition reaction that occurs when an alkene is treated with molecular bromine (Br2).

  • dehydrohalogenation

    An elimination reaction involving the loss of H and a halogen (such as Cl, Br, or I).

  • energy of activation

    In an energy diagram, the height of the energy barrier (the hump) between the reactants and the products.

  • keto-enol tautomerization

    The equilibrium that is established between an enol and a ketone in either acid-catalyzed or basecatalyzed conditions.

  • Nucleic acid

    A biopolymer containing three types of monomer units: heterocyclic aromatic amine bases derived from purine and pyrimidine, the monosaccharides d-ribose or 2-deoxy-d-ribose, and phosphoric acid

  • plastic

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

  • Polysaccharide

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

  • quintet

    In NMR spectroscopy, a signal that is comprised of five peaks.

  • radiotracer

    A radioisotope that can be used to trace the path of an element in a chemical system. (Section 21.5)

  • retention of configuration

    During a reaction, when the configuration of a chirality center remains unchanged.

  • stereoselective

    A reaction in which one substrate produces two stereoisomers in unequal amounts.

  • termolecular

    For mechanisms, a step that involves three chemical entities.

  • torsional angle

    The angle between two groups in a Newman projection, also called the dihedral angle.

  • Transition state

    The highest energy point on a reaction coordinate diagram. The chemical structure at this point is commonly called an activated complex.

  • Triol

    A compound containing three hydroxyl groups.

  • unsaturated

    A compound containingone or more p bonds.

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