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Solutions for Chapter 17.1: Nomenclature

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 17.1: Nomenclature

Solutions for Chapter 17.1
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This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Chapter 17.1: Nomenclature includes 2 full step-by-step solutions. Since 2 problems in chapter 17.1: Nomenclature have been answered, more than 27803 students have viewed full step-by-step solutions from this chapter. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741.

Key Chemistry Terms and definitions covered in this textbook
  • absorbance

    In UV-Vis spectroscopy, the value log (I0/I) where I0 is the intensity of the reference beam and I is the intensity of the sample beam.

  • Anabolic steroid

    A steroid hormone, such as testosterone, that promotes tissue and muscle growth and development

  • Bond dipole moment

    A measure of the polarity of a covalent bond. The product of the charge on either atom of a polar bond times the distance between the atoms

  • Born–Haber cycle

    A thermodynamic cycle based on Hess’s law that relates the lattice energy of an ionic substance to its enthalpy of formation and to other measurable quantities. (Section 8.2)

  • crossed aldol reaction

    An aldol reaction that occurs between different partners.

  • Diamagnetic current in NMR

    The circulation of electron density in a molecule in an applied magnetic fi eld.

  • Enantioselective reaction

    A reaction that produces one enantiomer in preference to the other.

  • Functional group

    An atom or group of atoms within a molecule that shows a characteristic set of physical and chemical properties

  • half-life

    The time required for the concentration of a reactant substance to decrease to half its initial value; the time required for half of a sample of a particular radioisotope to decay. (Sections 14.4 and 21.4)

  • Hückel’s rule

    The requirement for an odd number of p electron pairs in order for a compound to be aromatic.

  • lipid

    Naturally occurring compoundsthat can be extracted from cells usingnonpolar organic solvents.

  • methylene group

    A CH2 group.

  • nuclear binding energy

    The energy required to decompose an atomic nucleus into its component protons and neutrons. (Section 21.6)

  • nucleophilic acyl substitution

    A reaction in which a nucleophile attacks a carboxylic acid derivative.

  • oxidation number (oxidation state)

    A positive or negative whole number assigned to an element in a molecule or ion on the basis of a set of formal rules; to some degree it reflects the positive or negative character of that atom. (Section 4.4)

  • probability density 1c22

    A value that represents the probability that an electron will be found at a given point in space. Also called electron density. (Section 6.5)

  • S

    A term used to designate the configuration of a chirality center, determined in the following way: Each of the four groups is assigned a priority, and the molecule is then rotated (if necessary) so that the #4 group is directed behind the page (on a dash). A counterclockwise sequence for 1-2-3 is designated as S.

  • saturated hydrocarbon

    A hydrocarbon that contains no p bonds.

  • Solvolysis

    A nucleophilic substitution in which the solvent is also the nucleophile

  • substrate

    The starting alkyl halide in a substitution or elimination reaction.

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