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Solutions for Chapter 14: Applications of Ultraviolet -Visible Molecular Absorption SpectrQmetry

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 14: Applications of Ultraviolet -Visible Molecular Absorption SpectrQmetry

Solutions for Chapter 14
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Textbook: Principles of Instrumental Analysis
Edition: 6
Author: Douglas A. Skoog F. James Holler Stanley R. Crouch
ISBN: 9780495012016

Chapter 14: Applications of Ultraviolet -Visible Molecular Absorption SpectrQmetry includes 24 full step-by-step solutions. 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 24 problems in chapter 14: Applications of Ultraviolet -Visible Molecular Absorption SpectrQmetry have been answered, more than 51306 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
  • acylium ion

    The resonancestabilized, cationic intermediate of a Friedel-Crafts acylation, formed by treating an acyl halide with aluminum trichloride.

  • alcohol.

    An organic compound containing the hydroxyl group —OH. (24.4)

  • amino acids.

    A compound that contains at least one amino group and at least one carboxyl group. (25.3)

  • angstrom

    A common non-SI unit of length, denoted Å, that is used to measure atomic dimensions: 1Å = 10-10 m. (Section 2.3)

  • base

    A substance that is an H+ acceptor; a base produces an excess of OH-1aq2 ions when it dissolves in water. (Section 4.3)

  • body-centered lattice

    A crystal lattice in which the lattice points are located at the center and corners of each unit cell. (Section 12.2)

  • bond length

    The distance between the centers of two bonded atoms. (Section 8.3)

  • Chromatography

    A separation method involving passing a vapor or solution mixture through a column packed with a material with different affi nities for different components of the mixture.

  • complete ionic equation

    A chemical equation in which dissolved strong electrolytes (such as dissolved ionic compounds) are written as separate ions. (Section 4.2)

  • degree of substitution

    For alkenes, a classification method that refers to the number of alkyl groups connected to the double bond.

  • Disproportionation

    A termination process that involves the abstraction of a hydrogen atom from the beta position of the propagating radical of one chain by the radical endgroup of another chain.

  • Fischer projections

    A drawing style that is often used when dealing with compounds bearing multiple chirality centers, especially for carbohydrates. (See also Sect. 5.7.)

  • Hybridization

    The combination of atomic orbitals of different types

  • N terminus

    For a peptide chain,the end that contains the amino group.

  • nomenclature

    A system for naming organic compounds.

  • polar covalent bond

    A bond in which the difference in electronegative values of the two atoms is between 0.5 and 1.7.

  • quaternary ammonium salt

    An ionic compound containing a positively charged nitrogen atom connected to four alkyl groups.

  • resonance structures (resonance forms)

    Individual Lewis structures in cases where two or more Lewis structures are equally good descriptions of a single molecule. The resonance structures in such an instance are “averaged” to give a more accurate description of the real molecule. (Section 8.6)

  • third order

    A reaction that has a rate equation in which the sum of all exponents is three

  • Z

    For alkenes, a stereodescriptor that indicates that the two priority groups are on the same side of the p bond.