Solutions for Chapter 6: An Introduction to Spectrometric 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 6: An Introduction to Spectrometric Methods

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

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. Principles of Instrumental Analysis was written by Patricia and is associated to the ISBN: 9780495012016. Chapter 6: An Introduction to Spectrometric Methods includes 24 full step-by-step solutions. Since 24 problems in chapter 6: An Introduction to Spectrometric Methods have been answered, more than 3640 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • a-Amino acid

    An amino acid in which the amino group is on the carbon adjacent to the carboxyl group.

  • active site

    Specific site on a heterogeneous catalyst or an enzyme where catalysis occurs. (Section 14.7)

  • alpha (a) position

    The position immediately adjacent to a functional group.

  • Antibonding molecular orbital

    A molecular orbital in which electrons have a higher energy than they would in isolated atomic orbitals

  • bond cleavage

    The breaking of a bond, either homolytically or heterolytically. bond dissociation energy (Sect. 6.1): The energy required to achieve homolytic bond cleavage (generating radicals).

  • 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 length

    The number of times the cycle of chain propagation steps repeats in a chain reaction.

  • Chlorofl uorocarbons (CFCs, Freons)

    Compounds with one or two carbons, chlorine, and fl uorine, formerly used as refrigerants

  • Conjugate base

    The species formed when an acid transfers a proton to a base

  • degenerate orbitals

    Orbitals that have the same energy.

  • dipole moment (m)

    The amount of partial charge (d ) on either end of a dipole multiplied by the distance of separation (d): m=d × d

  • effusion

    The escape of a gas through an orifice or hole. (Section 10.8)

  • HOMO

    The highest occupied molecular orbital.

  • Molar absorptivity (e)

    The absorbance of a 1 M solution of a compound.

  • nucleosides

    The product formed when either d-ribose or 2-deoxy-d-ribose is coupled with certain nitrogen heterocycles (called bases).

  • polar reaction

    A reaction that involves the participation of ions as reactants, intermediates, or products.

  • salinity

    A measure of the salt content of seawater, brine, or brackish water. It is equal to the mass in grams of dissolved salts present in 1 kg of seawater. (Section 18.3)

  • saturated solution

    A solution in which undissolved solute and dissolved solute are in equilibrium. (Section 13.2)

  • Shielding in NMR

    Also called diamagnetic shielding; the term refers to the reduction in magnetic fi eld strength experienced by a nucleus underneath electron density induced to circulate when the molecule is placed in a strong magnetic fi eld.

  • symmetrical ether

    An ether (R!O!R) where both R groups are identical.

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