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Textbooks / Chemistry / Principles of Instrumental Analysis 6

Principles of Instrumental Analysis 6th Edition - Solutions by Chapter

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

Principles of Instrumental Analysis | 6th Edition - Solutions by Chapter

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

Principles of Instrumental Analysis was written by and is associated to the ISBN: 9780495012016. This textbook survival guide was created for the textbook: Principles of Instrumental Analysis , edition: 6. The full step-by-step solution to problem in Principles of Instrumental Analysis were answered by , our top Chemistry solution expert on 03/02/18, 06:21PM. Since problems from 34 chapters in Principles of Instrumental Analysis have been answered, more than 10721 students have viewed full step-by-step answer. This expansive textbook survival guide covers the following chapters: 34.

Key Chemistry Terms and definitions covered in this textbook
  • active site

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

  • anomers

    Stereoisomeric cyclic hemiacetals of an aldose or ketose that differ from each other in their configuration at the anomeric carbon.

  • antibonding molecular orbital.

    A molecular orbital that is of higher energy and lower stability than the atomic orbitals from which it was formed. (10.6)

  • Avogadro‚Äôs hypothesis

    A statement that equal volumes of gases at the same temperature and pressure contain equal numbers of molecules. (Section 10.3)

  • beta particles.

    See beta rays.

  • chelate effect

    The generally larger formation constants for polydentate ligands as compared with the corresponding monodentate ligands. (Section 23.3)

  • Claisen condensation

    A nucleophilic acyl substitution reaction in which the nucleophile is an ester enolate and the electrophile is an ester.

  • degenerate

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

  • electron-sea model

    A model for the behavior of electrons in metals. (Section 12.4)

  • enthalpy of formation

    The enthalpy change that accompanies the formation of a substance from the most stable forms of its component elements. (Section 5.7)

  • Fischer esterifi cation

    The process of forming an ester by refl uxing a carboxylic acid and an alcohol in the presence of an acid catalyst, commonly H2SO4, ArSO3H, or HCl

  • haloalkane

    An organic compound containing at least one halogen.

  • Lewis structures

    A drawing style inwhich the electrons take center stage.linear polymer (Sect. 27.6): A polymer thathas only a minimal amount of branching or nobranching at all.

  • nitrous acid

    A compound with molecular formula HONO.

  • Polarimeter

    An instrument for measuring the ability of a compound to rotate the plane of plane-polarized light.

  • Polarizability

    A measure of the ease of distortion of the distribution of electron density about an atom or group in response to interaction with other molecules or ions. Fluorine which has a high electronegativity and holds its electrons tightly, has a very low polarizability. Iodine, which has a lower electronegativity and holds its electrons less tightly, has a very high polarizability.

  • prostaglandins

    Lipids that contain 20 carbon atoms and are characterized by a five-membered ring with two side chains.

  • standard atmospheric pressure

    Defined as 760 torr or, in SI units, 101.325 kPa. (Section 10.2)

  • thioacetal

    A compound that contains two SR groups, both of which are connected to the same carbon atom.

  • van der Waals radius

    The minimum distance of approach to an atom that does not cause nonbonded interaction strain.

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