Solutions for Chapter 32: Radiochemical Methods

Principles of Instrumental Analysis | 6th Edition | ISBN: 9780495012016 | Authors: Douglas A. Skoog F. James Holler Stanley R. Crouch

Full solutions for Principles of Instrumental Analysis | 6th Edition

ISBN: 9780495012016

Principles of Instrumental Analysis | 6th Edition | ISBN: 9780495012016 | Authors: Douglas A. Skoog F. James Holler Stanley R. Crouch

Solutions for Chapter 32: Radiochemical Methods

Solutions for Chapter 32
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Textbook: Principles of Instrumental Analysis
Edition: 6
Author: Douglas A. Skoog F. James Holler Stanley R. Crouch
ISBN: 9780495012016

This textbook survival guide was created for the textbook: Principles of Instrumental Analysis , edition: 6. Principles of Instrumental Analysis was written by and is associated to the ISBN: 9780495012016. Since 20 problems in chapter 32: Radiochemical Methods have been answered, more than 6609 students have viewed full step-by-step solutions from this chapter. Chapter 32: Radiochemical Methods includes 20 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • atom.

    The basic unit of an element that can enter into chemical combination. (2.2)

  • beta (b) rays.

    Electrons. (2.2)

  • Chain propagation

    A step in a chain reaction characterized by the reaction of a reactive intermediate and a molecule to give a new reactive intermediate and a new molecule.

  • chain reaction

    A series of reactions in which one reaction initiates the next. (Section 21.7)

  • Chemical shift (d)

    The shift in parts per million of an NMR signal relative to the signal of TMS

  • coordination-sphere isomers

    Structural isomers of coordination compounds in which the ligands within the coordination sphere differ. (Section 23.4)

  • crystal-field theory

    A theory that accounts for the colors and the magnetic and other properties of transition-metal complexes in terms of the splitting of the energies of metal ion d orbitals by the electrostatic interaction with the ligands. (Section 23.6)

  • electron affinity

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

  • epimer

    Diastereomers that differ from each other in the configuration of only one chirality center.

  • flagpole interactions

    For cyclohexane, the steric interactions that occur between the flagpole hydrogen atoms in a boat conformation.

  • lipid

    Naturally occurring compoundsthat can be extracted from cells usingnonpolar organic solvents.

  • Molecular spectroscopy

    The study of which frequencies of radiation are absorbed or emitted by a particular substance and the correlation of these frequencies with details of molecular structure.

  • nomenclature

    A system for naming organic compounds.

  • plane of symmetry

    A plane that bisects a compound into two halves that are mirror images of each other.

  • Polyamide

    A polymer in which each monomer unit is joined to the next by an amide bond, as, for example, nylon 66.

  • quintet

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

  • structural proteins

    Fibrous proteins that are used for their structural rigidity. Examples include a-keratins found in hair, nails, skin, feathers, and wool.

  • sulfonate ions

    Common leaving groups. Examples include tosylate, mesylate, and triflate ions.

  • Transition state

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

  • Wolff-Kishner reduction

    Reduction of the C"O group of an aldehyde or ketone to a CH2 group using hydrazine and a base. Ylide (Section 16.6)

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