Solutions for Chapter 3.8: Axial and Equatorial Bonds in Cyclohexane

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 3.8: Axial and Equatorial Bonds in Cyclohexane

Solutions for Chapter 3.8
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This expansive textbook survival guide covers the following chapters and their solutions. Since 1 problems in chapter 3.8: Axial and Equatorial Bonds in Cyclohexane have been answered, more than 12519 students have viewed full step-by-step solutions from this chapter. Chapter 3.8: Axial and Equatorial Bonds in Cyclohexane includes 1 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741.

Key Chemistry Terms and definitions covered in this textbook
  • base

    A substance that is an H+ acceptor; a base produces an excess of OH-1aq2 ions when it dissolves in water. (Section 4.3)

  • Carbonyl group (Section 1.3C)

    A C"O group.

  • coupling constant

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

  • dipole moment (m)

    The amount of partial charge (d ) on either end of a dipole multiplied by the distance of separation (d): m=d × d

  • Eclipsed conformation

    A conformation about a carboncarbon single bond in which the atoms or groups on one carbon are as close as possible to the atoms or groups on an adjacent carbon.

  • entropy

    The measure of disorder associated with a system.

  • exothermic

    Any process with a negative DH (the system gives energy to the surroundings).

  • half-reaction

    An equation for either an oxidation or a reduction that explicitly shows the electrons involved, for example, Zn2 + 1aq2 + 2 e- ¡ Zn1s2. (Section 20.2)

  • Hydride ion

    A hydrogen atom with two electrons in its valence shell; H:!

  • isoprene

    2-Methyl-1,3-butadiene.

  • ketose

    A carbohydrate that contains a ketone group.

  • lambda max (lmax)

    In UVVis spectroscopy, the wavelength of maximum absorption.

  • lattice energy

    The energy required to separate completely the ions in an ionic solid. (Section 8.2)

  • Mercaptan

    A common name for a thiol; that is, any compound that contains an -SH (sulfhydryl) group

  • metallic bond

    Bonding, usually in solid metals, in which the bonding electrons are relatively free to move throughout the three-dimensional structure. (Section 8.1)

  • Monosaccharide

    A carbohydrate that cannot be hydrolyzed to a simpler carbohydrate.

  • nitrosonium ion

    The NO+ ion, which is formed when NaNO2 is treated with HCl.

  • Observed rotation

    the number of degrees through which a compound rotates the plane of polarized light

  • regiochemistry

    A term describing a consideration that must be taken into account for a reaction in which two or more constitutional isomers can be formed.

  • 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.

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