Solutions for Chapter 5.2: The Nomenclature of Alkenes

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 8th Edition

ISBN: 9780134042282

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 5.2: The Nomenclature of Alkenes

Solutions for Chapter 5.2
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Chapter 5.2: The Nomenclature of Alkenes includes 1 full step-by-step solutions. Organic Chemistry was written by Patricia and is associated to the ISBN: 9780134042282. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. Since 1 problems in chapter 5.2: The Nomenclature of Alkenes have been answered, more than 12137 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
  • acid.

    A substance that yields hydrogen ions (H1) when dissolved in water. (2.7)

  • aldonic acid

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

  • Brønsted base.

    A substance capable of accepting a proton. (4.3)

  • Carboxylic ester

    A derivative of a carboxylic acid in which H of the carboxyl group is replaced by a carbon.

  • Dienophile

    A compound containing a double bond (consisting of one or two C, N, or O atoms) that can react with a conjugated diene to give a Diels-Alder adduct.

  • enthalpy of reaction

    The enthalpy change associated with a chemical reaction. (Section 5.4)

  • fibers

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

  • First ionization potential

    The energy needed to remove the most loosely held electron from an atom or molecule.

  • Friedel-Crafts reaction

    An electrophilic aromatic substitution in which a hydrogen of an aromatic ring is replaced by an alkyl or acyl group.

  • Heterolytic bond cleavage

    Cleavage of a bond so that one fragment retains both electrons and the other retains none.

  • high-resolution mass spectrometry

    A technique that involves the use of a detector that can measure the m/z values to four decimal places.This technique allows for the determination of the molecular formula of an unknown compound.

  • instantaneous rate

    The reaction rate at a particular time as opposed to the average rate over an interval of time. (Section 14.2)

  • ionization energy

    The energy required to remove an electron from a gaseous atom when the atom is in its ground state. (Section 7.4)

  • Ketose

    A monosaccharide containing a ketone group.

  • nucleus

    The very small, very dense, positively charged portion of an atom; it is composed of protons and neutrons. (Section 2.2)

  • primary structure

    The sequence of amino acids along a protein chain. (Section 24.7)

  • racemic mixture

    A mixture of equal amounts of the dextrorotatory and levorotatory forms of a chiral molecule. A racemic mixture will not rotate the plane of polarized light. (Section 23.4)

  • spin-spin splitting

    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.

  • strong deactivators

    Groups that strongy deactivate an aromatic ring toward electrophilic aromatic substitution, thereby significantly decreasing the rate of the reaction.

  • sulfoxide

    A compound containing an SRO bond that is flanked on both sides by R groups.

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