Solutions for Chapter 15: Molecular Luminescence 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 15: Molecular Luminescence Spectrometry

This textbook survival guide was created for the textbook: Principles of Instrumental Analysis , edition: 6. Since 16 problems in chapter 15: Molecular Luminescence Spectrometry have been answered, more than 5006 students have viewed full step-by-step solutions from this chapter. Principles of Instrumental Analysis was written by Patricia and is associated to the ISBN: 9780495012016. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 15: Molecular Luminescence Spectrometry includes 16 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • acidic anhydride (acidic oxide)

    An oxide that forms an acid when added to water; soluble nonmetal oxides are acidic anhydrides. (Section 22.5)

  • adrenocortical hormones

    Hormones that are secreted by the cortex (the outer layer) of the adrenal glands. Adrenocortical hormones are typically characterized by a carbonyl group or hydroxyl group at C11 of the steroid skeleton.

  • alditol

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

  • alkene

    A compound that possesses a carbon-carbon double bond.

  • Alkyl group

    A group derived by removing a hydrogen from an alkane; given the symbol R!

  • aromatic

    A compound containing a planar ring of continuously overlapping p orbitals with 4n+2p electrons.

  • chemical equilibrium.

    A state in which the rates of the forward and reverse reactions are equal. (14.1)

  • cholesteric liquid crystalline phase

    A liquid crystal formed from flat, disc-shaped molecules that align through a stacking of the molecular discs. (Section 11.7)

  • cycloaddition reactions

    Reactions in which two p systems are joined together in a way that forms a ring. In the process, two p bonds are converted into two s bonds.

  • diamagnetism

    The circulation of electron density in the presence of an external magnetic field, which produces a local (induced) magnetic field that opposes the external magnetic field.

  • Edman degradation

    A method for analyzing the sequence of amino acids in apeptide by removing one amino acid residue at a time and identifying each residue as it is removed.

  • fishhook arrow

    A curved arrow with only one barb, indicating the motion of just one electron (also see Sect. 11.1).

  • Ketone

    A compound containing a carbonyl group bonded to two carbons.

  • matter

    Anything that occupies space and has mass; the physical material of the universe. (Section 1.1)

  • mean free path

    The average distance traveled by a gas molecule between collisions. (Section 10.8)

  • Newman projection

    A way to view a molecule by looking along a carbon-carbon single bond

  • reactant

    A starting substance in a chemical reaction; it appears to the left of the arrow in a chemical equation. (Section 3.1)

  • S (Section 3.3

    From the Latin, sinister, left; used in the R,S convention to show that the order of priority of groups on a chiral center is counterclockwise

  • Thermochemistry

    The study of the energy of chemical structures.

  • weak activators

    Groups that weakly activate an aromatic ring toward electrophilic aromatic substitution, thereby enhancing the rate of the reaction.

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