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Solutions for Chapter 8.1: Functional Group Transformation by Nucleophilic Substitution

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 8.1: Functional Group Transformation by Nucleophilic Substitution

Solutions for Chapter 8.1
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Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Since 1 problems in chapter 8.1: Functional Group Transformation by Nucleophilic Substitution have been answered, more than 27766 students have viewed full step-by-step solutions from this chapter. Chapter 8.1: Functional Group Transformation by Nucleophilic Substitution includes 1 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • 1,2-addition

    A reaction involving the addition of two groups to a conjugated p system in which one group is installed at the C1 position and the other group is installed at the C2 position.

  • alkali metals

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

  • Allylic

    Next to a carbon-carbon double bond.

  • Arene

    A term used to classify benzene and its derivatives.

  • autoionization

    The process whereby water spontaneously forms low concentrations of H+1aq2 and OH-1aq2 ions by proton transfer from one water molecule to another. (Section 16.3)

  • broadband decoupling

    In 13C NMR spectroscopy, a technique in which all 13C!1H splitting is suppressed with the use of two rf transmitters.

  • Conjugated

    A conjugated diene or carbonyl is one in which the double bonds are separated by one single bond

  • coordination number

    The number of adjacent atoms to which an atom is directly bonded. In a complex the coordination number of the metal ion is the number of donor atoms to which it is bonded. (Sections 12.37 and 24.2)

  • deoxyribonucleic acid (DNA)

    A polynucleotide in which the sugar component is deoxyribose. (Section 24.10)

  • equatorial position

    For chair conformations of substituted cyclohexanes, a position that is approximately along the equator of the ring.

  • Faraday constant (F )

    The magnitude of charge of one mole of electrons: 96,500 C>mol. (Section 20.5)

  • flagpole interactions

    For cyclohexane, the steric interactions that occur between the flagpole hydrogen atoms in a boat conformation.

  • immiscible liquids

    Liquids that do not dissolve in one another to a significant extent. (Section 13.3)

  • intensive property

    A property that is independent of the amount of material considered, for example, density. (Section 1.3)

  • l-Monosaccharide

    A monosaccharide that, when written as a Fischer projection, has the !OH on its penultimate carbon to the left.

  • normal melting point

    The melting point at 1 atm pressure. (Section 11.6)

  • phosphatidic acid

    A phosphoric monoester, which is the simplest kind of phosphoglyceride.

  • Polyamide

    A polymer in which each monomer unit is joined to the next by an amide bond, as, for example, nylon 66.

  • van der Waals radius

    The minimum distance of approach to an atom that does not cause nonbonded interaction strain.

  • vibrational excitation

    In IR spectroscopy, the energy of a photon is absorbed and temporarily stored as vibrational energy

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