Solutions for Chapter 10: Atomic Emission Spectrometry

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 10: Atomic Emission Spectrometry

This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Principles of Instrumental Analysis , edition: 6. Chapter 10: Atomic Emission Spectrometry includes 14 full step-by-step solutions. Principles of Instrumental Analysis was written by Patricia and is associated to the ISBN: 9780495012016. Since 14 problems in chapter 10: Atomic Emission Spectrometry have been answered, more than 4208 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • Aldose

    A monosaccharide containing an aldehyde group

  • alkaloids

    Naturally occurring amines isolated from plants.

  • Born-Haber cycle.

    The cycle that relates lattice energies of ionic compounds to ionization energies, electron affinities, heats of sublimation and formation, and bond enthalpies. (9.3)

  • chain reaction

    A reaction (generally involving radicals) in which one chemical entity can ultimately cause a chemical transformation for thousands of molecules.

  • conservation of orbital symmetry

    During a reaction, the requirement that the phases of the frontier MOs must be aligned.

  • coordination number

    The number of adjacent atoms to which an atom is directly bonded. In a complex the coordination number of the metal ion is the number of donor atoms to which it is bonded. (Sections 12.37 and 24.2)

  • critical temperature (Tc).

    The temperature above which a gas will not liquefy. (11.8)

  • diamagnetic.

    Repelled by a magnet; a diamagnetic substance contains only paired electrons. (7.8)

  • elimination (of radicals)

    In radical reaction mechanisms, a step in which a bond forms between the alpha (a) and beta (b) positions. As a result, a single bond at the b position is cleaved, causing the compound to fragment into two pieces.

  • enamine

    A compound containing a nitrogen atom directly connected to a carboncarbon p bond.

  • fingerprint region

    The region of an IR spectrum that contains signals resulting from the vibrational excitation of most single bonds (stretching and bending).

  • heterolytic bond cleavage

    Bond breaking that results in the formation of ions.

  • hydroxyl group

    An OH group.

  • mass spectrometer

    An instrument used to measure the precise masses and relative amounts of atomic and molecular ions. (Section 2.4)

  • Melt transition (Tm)

    The temperature at which crystalline regions of a polymer melt.

  • oxaphosphetane

    An intermediate that is believed to be formed during Wittig reactions.

  • quaternary structure

    The structure of a protein resulting from the clustering of several individual protein chains into a final specific shape. (Section 24.7)

  • silicates

    Compounds containing silicon and oxygen, structurally based on SiO4 tetrahedra. (Section 22.10)

  • Stereoselective reaction

    A reaction in which one stereoisomer is formed in preference to all others. A stereoselective reaction may be enantioselective or diastereoselective, as the case may be.

  • Williamson ether synthesis

    A method for preparing an ether from an alkoxide ion and an alkyl halide (via an SN2 process).

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