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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 Patricia and is associated to the ISBN: 9780495012016. Since 20 problems in chapter 32: Radiochemical Methods have been answered, more than 2795 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
  • 1,4-addition

    A reaction involving the addition of two groups to a conjugated p system in which one group is installed at the C1 position and the other group is installed at the C4 position.

  • aldonic acid

    The product obtained when the aldehyde group of an aldose is oxidized.

  • Alkylation reaction

    Any reaction in which a new carbon-carbon bond to an alkyl group is formed.

  • Aprotic acid

    An acid that is not a proton donor; an acid that is an electron pair acceptor in a Lewis acid-base reaction.

  • carboxylic acid

    A compound that contains the ¬COOH functional group. (Sections 16.10 and 24.4)

  • Chiral center

    A tetrahedral atom, most commonly carbon, that is bonded to four different groups; also called a chirality center

  • degenerate

    A situation in which two or more orbitals have the same energy. (Section 6.7)

  • deoxyribonucleic acid (DNA)

    A polynucleotide in which the sugar component is deoxyribose. (Section 24.10)

  • dextrorotatory, or merely dextro or d

    A term used to label a chiral molecule that rotates the plane of polarization of plane-polarized light to the right (clockwise). (Section 23.4)

  • electrophile

    A compound containing an electron-deficient atom that is capable of accepting a pair of electrons.

  • energy-level diagram

    A diagram that shows the energies of molecular orbitals relative to the atomic orbitals from which they are derived. Also called a molecular-orbital diagram. (Section 9.7)

  • extensive property

    A property that depends on the amount of material considered; for example, mass or volume. (Section 1.3)

  • living polymer

    A polymer that isformed via anionic polymerization.

  • magic numbers

    Numbers of protons and neutrons that result in very stable nuclei. (Section 21.2)

  • norbornane

    The common name for bicyclo[2.2.1]heptane.

  • oxidation–reduction (redox) reaction

    A chemical reaction in which the oxidation states of certain atoms change. (Section 4.4; Chapter 20: Introduction)

  • polar aprotic solvent

    A solvent that lacks hydrogen atoms connected directly to an electronegative atom.

  • qualitative analysis

    The determination of the presence or absence of a particular substance in a mixture. (Section 17.7)

  • Rearrangement

    A change in connectivity of the atoms in a product compared with the con nectivity of the same atoms in the starting material.

  • Regioselective reaction

    An addition or substitution reaction in which one of two or more possible products is formed in preference to all others that might be formed.

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