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Solutions for Chapter 3: Stoichiometry of Formulas and Equations

Chemistry: The Molecular Nature of Matter and Change | 5th Edition | ISBN: 9780077216504 | Authors: Martin S. Silberberg

Full solutions for Chemistry: The Molecular Nature of Matter and Change | 5th Edition

ISBN: 9780077216504

Chemistry: The Molecular Nature of Matter and Change | 5th Edition | ISBN: 9780077216504 | Authors: Martin S. Silberberg

Solutions for Chapter 3: Stoichiometry of Formulas and Equations

Solutions for Chapter 3
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Textbook: Chemistry: The Molecular Nature of Matter and Change
Edition: 5
Author: Martin S. Silberberg
ISBN: 9780077216504

Chemistry: The Molecular Nature of Matter and Change was written by and is associated to the ISBN: 9780077216504. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 3: Stoichiometry of Formulas and Equations includes 62 full step-by-step solutions. Since 62 problems in chapter 3: Stoichiometry of Formulas and Equations have been answered, more than 79047 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Chemistry: The Molecular Nature of Matter and Change, edition: 5.

Key Chemistry Terms and definitions covered in this textbook
  • blocking group

    A group that can be readily installed and uninstalled. Used for regiochemical control during synthesis.

  • bond length

    The distance between the centers of two bonded atoms. (Section 8.3)

  • chelate effect

    The generally larger formation constants for polydentate ligands as compared with the corresponding monodentate ligands. (Section 23.3)

  • coordination compound

    A compound containing a metal ion bonded to a group of surrounding molecules or ions that act as ligands. (Section 23.2)

  • coordination sphere

    The metal ion and its surrounding ligands. (Section 23.2)

  • electron capture

    A mode of radioactive decay in which an inner-shell orbital electron is captured by the nucleus. (Section 21.1)

  • functional group

    A characteristic group of atoms/bonds that possess a predictable chemical behavior.

  • gray (Gy)

    The SI unit for radiation dose

  • Hertz (Hz)

    The unit in which frequency is measured: s 21 (read “per second”).

  • Heterocycle

    A cyclic compound whose ring contains more than one kind of atom. Oxirane (ethylene oxide), for example, is a heterocycle whose ring contains two carbon atoms and one oxygen atom.

  • Hydride ion

    A hydrogen atom with two electrons in its valence shell; H:!

  • hydrophobic

    Water repelling. The term is often used to describe a type of colloid. (Section 13.6)

  • Line-angle formula

    An abbreviated way to draw structural formulas in which vertices and line endings represent carbons

  • Merrifield synthesis

    A method for building a peptide from protected building blocks.

  • organic chemistry

    The study of carbon-containing compounds, typically containing carbon–carbon bonds. (Section 2.9; Chapter 24:Introduction)

  • pyrimidine

    A compound that is similar in structure to pyridine but contains one extra nitrogen atom at the 3 position.

  • specific heat 1Cs2

    The heat capacity of 1 g of a substance; the heat required to raise the temperature of 1 g of a substance by 1 °C. (Section 5.5)

  • thermosetting resins

    Highly crosslinked polymers that are generally very hard and insoluble.

  • three-center, two-electron bonds

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

  • Williamson ether synthesis

    A general method for the synthesis of dialkyl ethers by an SN2 reaction between a haloalkane and an alkoxide ion.

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