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Solutions for Chapter 7: Quantum Theory and Atomic Structure

Chemistry: The Molecular Nature of Matter and Change - Standalone book | 7th Edition | ISBN: 9780073511177 | Authors: Martin Silberberg Dr., Patricia Amateis Professor

Full solutions for Chemistry: The Molecular Nature of Matter and Change - Standalone book | 7th Edition

ISBN: 9780073511177

Chemistry: The Molecular Nature of Matter and Change - Standalone book | 7th Edition | ISBN: 9780073511177 | Authors: Martin Silberberg Dr., Patricia Amateis Professor

Solutions for Chapter 7: Quantum Theory and Atomic Structure

Solutions for Chapter 7
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Textbook: Chemistry: The Molecular Nature of Matter and Change - Standalone book
Edition: 7
Author: Martin Silberberg Dr., Patricia Amateis Professor
ISBN: 9780073511177

This expansive textbook survival guide covers the following chapters and their solutions. Chapter 7: Quantum Theory and Atomic Structure includes 96 full step-by-step solutions. Chemistry: The Molecular Nature of Matter and Change - Standalone book was written by and is associated to the ISBN: 9780073511177. This textbook survival guide was created for the textbook: Chemistry: The Molecular Nature of Matter and Change - Standalone book, edition: 7. Since 96 problems in chapter 7: Quantum Theory and Atomic Structure have been answered, more than 37384 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • alkynes

    Compounds containing a carbon-carbon triple bond.

  • battery.

    A galvanic cell, or a series of combined galvanic cells, that can be used as a source of direct electric current at a constant voltage. (18.6)

  • Beer’s law

    The light absorbed by a substance (A) equals the product of its extinction coefficient 1e2, the path length through which the light passes (b), and the molar concentration of the substance (c): A = ebc. (Section 14.2)

  • broadband decoupling

    In 13C NMR spectroscopy, a technique in which all 13C!1H splitting is suppressed with the use of two rf transmitters.

  • carbocation

    An intermediate containing a positively charged carbon atom.

  • Carboxylic ester

    A derivative of a carboxylic acid in which H of the carboxyl group is replaced by a carbon.

  • Chain-growth polymerization

    A polymerization that involves sequential addition reactions, either to unsaturated monomers or to monomers possessing other reactive functional groups.

  • Claisen rearrangement

    A [3,3] sigmatropic rearrangement that is observed for allylic vinylic ethers.

  • Confi guration

    Refers to the arrangement of atoms about a stereocenter

  • Downfield

    A signal of an NMR spectrum that is shifted toward the left (larger chemical shift) on the chart paper.

  • electrochemistry

    The branch of chemistry that deals with the relationships between electricity and chemical reactions. (Chapter 20: Introduction)

  • elimination

    A reaction involving the loss of a leaving group and formation of a p bond.

  • fishhook arrow

    A curved arrow with only one barb, indicating the motion of just one electron (also see Sect. 11.1).

  • Hybrid orbital

    An orbital formed by the combination of two or more atomic orbitals.

  • paramagnetism

    A property that a substance possesses if it contains one or more unpaired electrons. A paramagnetic substance is drawn into a magnetic field. (Section 9.8)

  • Reaction mechanism

    A step-by-step description of how a chemical reaction occurs.

  • saponification

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

  • Strecker synthesis

    A synthetictechnique for preparing racemic a-amino acidsfrom aldehydes.

  • three-center, two-electron bonds

    A bond in which two electrons are associated with three atoms, such as in diborane (B2H6).

  • van der Waals radius

    The minimum distance of approach to an atom that does not cause nonbonded interaction strain.

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