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Solutions for Chapter 2.15: Applying the IUPAC Rules: The Names of the C6H14 Isomers

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 2.15: Applying the IUPAC Rules: The Names of the C6H14 Isomers

Solutions for Chapter 2.15
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Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. Chapter 2.15: Applying the IUPAC Rules: The Names of the C6H14 Isomers includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 2.15: Applying the IUPAC Rules: The Names of the C6H14 Isomers have been answered, more than 7359 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • atomic number (Z).

    The number of protons in the nucleus of an atom. (2.3)

  • basic anhydride (basic oxide)

    An oxide that forms a base when added to water; soluble metal oxides are basic anhydrides. (Section 22.5)

  • carbon black

    A microcrystalline form of carbon. (Section 22.9)

  • catalyst.

    A substance that increases the rate of a chemical reaction without itself being consumed. (13.6)

  • chiral.

    Compounds or ions that are not superimposable with their mirror images. (23.4)

  • copolymer.

    A polymer containing two or more different monomers. (25.2)

  • coupling constant

    When signal splitting occurs in NMR spectroscopy, the distance between the individual peaks of a signal.

  • dihedral angle

    The angle by which two groups are separated in a Newman projection.

  • enantiomer

    A nonsuperimposable mirror image.

  • hydrolysis

    A reaction in which bonds are cleaved by treatment with water.

  • intermolecular forces

    The attractive forces between molecules.

  • ketose

    A carbohydrate that contains a ketone group.

  • lambda max (lmax)

    In UVVis spectroscopy, the wavelength of maximum absorption.

  • nitration

    An electrophilic aromatic substitution reaction that involves the installation of a nitro group (NO2) on an aromatic ring.

  • Pauli exclusion principle

    No more than two electrons may be present in an orbital. If two electrons are present, their spins must be paired

  • pyrometallurgy

    A process in which heat converts a mineral in an ore from one chemical form to another and eventually to the free metal. (Section 23.2)

  • quantitative analysis

    The determination of the amount of a given substance that is present in a sample. (Section 17.7)

  • Schiff base

    An alternative name for an imine

  • solvent extraction

    A process by which one or more compounds are removed from a mixture of organic compounds, based on a difference in solubility and/or acid-base properties.

  • terminal alkynes

    Compounds with the following structure: R!C#C!H

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