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Solutions for Chapter 14: Mass Spectrometry, Infrared Spectroscopy, and Ultraviolet/Visible Spectroscopy

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9780321803221

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 14: Mass Spectrometry, Infrared Spectroscopy, and Ultraviolet/Visible Spectroscopy

Solutions for Chapter 14
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Textbook: Organic Chemistry
Edition: 7
Author: Paula Yurkanis Bruice
ISBN: 9780321803221

This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Since 31 problems in chapter 14: Mass Spectrometry, Infrared Spectroscopy, and Ultraviolet/Visible Spectroscopy have been answered, more than 18682 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by and is associated to the ISBN: 9780321803221. Chapter 14: Mass Spectrometry, Infrared Spectroscopy, and Ultraviolet/Visible Spectroscopy includes 31 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alkylation

    A reaction that achieves the installation of an alkyl group. For example, an SN2 reaction in which an alkyl group is connected to an attacking nucleophile.

  • anode

    An electrode at which oxidation occurs. (Section 20.3)

  • Aryl group (Ar -)

    A group derived from an arene by removal of an H.

  • Bonding electrons

    Valence electrons involved in forming a covalent bond (i.e., shared electrons).

  • Brønsted–Lowry base

    A substance (molecule or ion) that acts as a proton acceptor. (Section 16.2)

  • chemical equation

    A representation of a chemical reaction using the chemical formulas of the reactants and products; a balanced chemical equation contains equal numbers of atoms of each element on both sides of the equation. (Section 3.1)

  • chemical formula

    A notation that uses chemical symbols with numerical subscripts to convey the relative proportions of atoms of the different elements in a substance. (Section 2.6)

  • fibers

    Strands of a polymer that are generated when the polymer is heated, forced through small holes, and then cooled.

  • law of definite proportions

    A law that states that the elemental composition of a pure substance is always the same, regardless of its source; also called the law of constant composition. (Section 1.2)

  • nonelectrolyte

    A substance that does not ionize in water and consequently gives a nonconducting solution. (Section 4.1)

  • nuclear model

    Model of the atom with a nucleus containing protons and neutrons and with electrons in the space outside the nucleus. (Section 2.2)

  • Orthogonal

    Having no net overlap.

  • polydentate ligand

    A ligand in which two or more donor atoms can coordinate to the same metal ion. (Section 23.3)

  • Primary structure of nucleic acids

    The sequence of bases along the pentose-phosphodiester backbone of a DNA or RNA molecule read from the 5’ end to the 3’ end

  • protein

    A biopolymer formed from amino acids. (Section 24.7)

  • resonance stabilization

    The stabilization associated with the delocalization of electrons via resonance.

  • retro Diels-Alder reaction

    The reverse of a Diels-Alder reaction, achieved at high temperature. A cyclohexene derivative is converted into a diene and a dienophile.

  • Schiemann reaction

    The conversion of an aryl diazonium salt into fluorobenzene upon treatment with fluoroboric acid (HBF4).

  • Steric strain

    The strain that arises when nonbonded atoms separated by four or more bonds are forced closer to each other than their atomic (contact) radii would allow. Steric strain is also called non-bonded interaction strain, or van der Waals strain.

  • Valence Bond Theory

    A model of bonding that places electron pairs between adjacent atoms to create bonds.

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