Solutions for Chapter 2.3: Using Scientific Measurements

Modern Chemistry: Student Edition 2012 | 1st Edition | ISBN: 9780547586632 | Authors: Jerry L. Sarquis, Mickey Sarquis

Full solutions for Modern Chemistry: Student Edition 2012 | 1st Edition

ISBN: 9780547586632

Modern Chemistry: Student Edition 2012 | 1st Edition | ISBN: 9780547586632 | Authors: Jerry L. Sarquis, Mickey Sarquis

Solutions for Chapter 2.3: Using Scientific Measurements

Modern Chemistry: Student Edition 2012 was written by and is associated to the ISBN: 9780547586632. Chapter 2.3: Using Scientific Measurements includes 10 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Modern Chemistry: Student Edition 2012, edition: 1. Since 10 problems in chapter 2.3: Using Scientific Measurements have been answered, more than 24122 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • actinide series.

    Elements that have incompletely filled 5f subshells or readily give rise to cations that have incompletely filled 5f subshells. (7.9)

  • Chain-growth polymerization

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

  • condensation polymerization

    Polymerization in which molecules are joined together through condensation reactions. (Section 12.8)

  • dilution.

    A procedure for preparing a less concentrated solution from a more concentrated solution. (4.5)

  • downfield

    The left side of an NMR spectrum.

  • electrostatic potential maps

    A three-dimensional, rainbowlike image used to visualize partial charges in a compound.

  • energy of activation

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

  • ferromagnetism

    A form of magnetism in which unpaired electron spins align parallel to one another. (Section 23.1)

  • glass

    An amorphous solid formed by fusion of SiO2, CaO, and Na2O. Other oxides may also be used to form glasses with differing characteristics. (Section 22.10)

  • hydride ion

    An ion formed by the addition of an electron to a hydrogen atom: H-. (Section 7.7)

  • isolated diene

    A compound containing two carbon-carbon p bonds that are separated by two or more s bonds.

  • levorotatory, or merely levo or l

    A term used to label a chiral molecule that rotates the plane of polarization of plane-polarized light to the left (counterclockwise). (Section 24.4)

  • molecular orbital (MO)

    An allowed state for an electron in a molecule. According to molecular-orbital theory, a molecular orbital is entirely analogous to an atomic orbital, which is an allowed state for an electron in an atom. Most bonding molecular orbitals can be classified as s or p, depending on the disposition of electron density with respect to the internuclear axis. (Section 9.7)

  • Mutarotation

    The change in specifi c rotation that occurs when an a or b hemiacetal form of a carbohydrate in aqueous solution is converted to an equilibrium mixture of the two forms.

  • 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)

  • polarizability

    The ease with which the electron cloud of an atom or a molecule is distorted by an outside influence, thereby inducing a dipole moment. (Section 11.2)

  • Reactive intermediate

    A high-energy species formed between two successive reaction steps, that lies in an energy minimum between the two transition states

  • 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.

  • terminal alkynes

    Compounds with the following structure: R!C#C!H

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