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Solutions for Chapter Chapter 1: Chemical Measurements

Quantitative Chemical Analysis | 8th Edition | ISBN: 9781429218153 | Authors: Daniel C. Harris

Full solutions for Quantitative Chemical Analysis | 8th Edition

ISBN: 9781429218153

Quantitative Chemical Analysis | 8th Edition | ISBN: 9781429218153 | Authors: Daniel C. Harris

Solutions for Chapter Chapter 1: Chemical Measurements

Solutions for Chapter Chapter 1
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Textbook: Quantitative Chemical Analysis
Edition: 8
Author: Daniel C. Harris
ISBN: 9781429218153

Quantitative Chemical Analysis was written by and is associated to the ISBN: 9781429218153. This textbook survival guide was created for the textbook: Quantitative Chemical Analysis, edition: 8. Chapter Chapter 1: Chemical Measurements includes 51 full step-by-step solutions. Since 51 problems in chapter Chapter 1: Chemical Measurements have been answered, more than 49838 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • addition polymerization

    Polymerization that occurs through coupling of monomers with one another, with no other products formed in the reaction. (Section 12.8)

  • allylic

    The positions that are adjacent to the vinylic positions of a carboncarbon double bond.

  • Allylic substitution

    Any reaction in which an atom or group of atoms is substituted for another atom or group of atoms at an allylic carbon.

  • boranes

    Covalent hydrides of boron. (Section 22.11)

  • crystalline solid (crystal)

    A solid whose internal arrangement of atoms, molecules, or ions possesses a regularly repeating pattern in any direction through the solid. (Section 12.2)

  • Dextrorotatory

    Refers to a substance that rotates the plane of polarized light to the right

  • E

    For alkenes, a stereodescriptorthat indicates that the two priority groups are on opposite sides of the p bond.

  • electron affinity

    The energy change that occurs when an electron is added to a gaseous atom or ion. (Section 7.5)

  • electron capture

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

  • enolate

    The resonance-stabilized conjugate base of a ketone, aldehyde, or ester.

  • 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)

  • Micelle

    A spherical arrangement of organic molecules in water solution clustered so that their hydrophobic parts are buried inside the sphere and their hydrophilic parts are on the surface of the sphere and in contact with water

  • N-bromosuccinimide

    A reagent used for allylic bromination to avoid a competing reaction in which bromine adds across the p bond.

  • nucleon

    A particle found in the nucleus of an atom. (Section 21.1)

  • optically pure

    A solution containing just one enantiomer, but not its mirror image.

  • reductive amination

    The conversion of a ketone or aldehyde into an imine under conditions in which the imine is reduced as soon as it is formed, giving an amine.

  • staggered conformation

    A conformation in which nearby groups in a Newman projection have a dihedral angle of 60°.

  • strong deactivators

    Groups that strongy deactivate an aromatic ring toward electrophilic aromatic substitution, thereby significantly decreasing the rate of the reaction.

  • Tertiary structure of proteins

    The three-dimensional arrangement in space of all atoms in a single polypeptide chain.

  • Transition state

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

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