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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 13018 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
  • alkali metals

    Members of group 1A in the periodic table. (Section 7.7)

  • Anti conformation

    A conformation about a single bond in which two groups on adjacent carbons lie at a dihedral angle of 180°.

  • azide synthesis

    A method for preparing primary amines that avoids the formation of secondary and tertiary amines.

  • boiling-point elevation (DTb).

    The boiling point of the solution (Tb) minus the boiling point of the pure solvent (T° b). (12.6)

  • chair conformation

    The lowest energy conformation for cyclohexane, in which all bond angles are fairly close to 109.5° and all hydrogen atoms are staggered.

  • Conjugate base

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

  • coupling (of protons)

    A phenomenon observed most commonly for nonequivalent protons connected to adjacent carbon atoms in which the multiplicity of each signal is affected by the other.

  • d sugar

    A carbohydrate for whichthe chirality center farthest from the carbonylgroup will have an OH group pointing to theright in the Fischer projection.

  • Double-headed arrow

    A symbol used to show that structures on either side of it are resonance-contributing structures

  • fibrous proteins

    Proteins that consist of linear chains that are bundled together.

  • fission

    The splitting of a large nucleus into two smaller ones. (Section 21.6)

  • Glycosidic bond

    The bond from the anomeric carbon of a glycoside to an !OR group

  • hyperconjugation

    An effect that explains why alkyl groups stabilize a carbocation.

  • imidazole

    A compound containing a five-membered ring that is similar to pyrrole but has one extra nitrogen atom at the 3 position.

  • isoelectric point (pI)

    For an amino acid, the specific pH at which the concentration of the zwitterionic form reaches its maximum value.

  • photosynthesis

    The process that occurs in plant leaves by which light energy is used to convert carbon dioxide and water to carbohydrates and oxygen. (Section 23.3)

  • Rearrangement

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

  • steroids

    Lipids that are based on a tetracyclic ring system involving three six-membered rings and one five-membered ring. Cholesterol is an example.

  • thiols

    Compounds containing a mercapto group (SH).

  • Triglyceride (triacylglycerol)

    An ester of glycerol with three fatty acids

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