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Solutions for Chapter 23.4: spectroscopy of amiNes

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Full solutions for Organic Chemistry | 6th Edition

ISBN: 9781936221349

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Solutions for Chapter 23.4: spectroscopy of amiNes

Since 3 problems in chapter 23.4: spectroscopy of amiNes have been answered, more than 18369 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by and is associated to the ISBN: 9781936221349. Chapter 23.4: spectroscopy of amiNes includes 3 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6.

Key Chemistry Terms and definitions covered in this textbook
  • active site

    Specific site on a heterogeneous catalyst or an enzyme where catalysis occurs. (Section 14.7)

  • alkylation

    A reaction that achieves the installation of an alkyl group. For example, an SN2 reaction in which an alkyl group is connected to an attacking nucleophile.

  • Anomeric carbon

    The hemiacetal or acetal carbon of the cyclic form of a carbohydrate

  • aromatic hydrocarbons

    Hydrocarbon compounds that contain a planar, cyclic arrangement of carbon atoms linked by both s and delocalized p bonds. (Section 24.2)

  • band gap

    The energy gap between a fully occupied band called a valence band and an empty band called the conduction band. (Section 12.7)

  • basic anhydride (basic oxide)

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

  • beta (b) position

    The position immediately adjacent to an alpha (a) position.

  • bicyclic

    A structure containing two rings that are fused together.

  • chlorophyll

    A plant pigment that plays a major role in conversion of solar energy to chemical energy in photosynthesis. (Section 23.3)

  • collision model

    A model of reaction rates based on the idea that molecules must collide to react; it explains the factors influencing reaction rates in terms of the frequency of collisions, the number of collisions with energies exceeding the activation energy, and the probability that the collisions occur with suitable orientations. (Section 14.5)

  • cumulated diene

    A compound containing two adjacent p bonds.

  • dipole

    A molecule with one end having a partial negative charge and the other end having a partial positive charge; a polar molecule. (Section 8.4)

  • Enamine

    An unsaturated compound derived by the reaction of an aldehyde or ketone and a secondary amine followed by loss of H2O; R2C"CR!NR2

  • Mass spectrum

    A plot of the relative abundance of ions versus their mass-to-charge ratio

  • Micelle

    A spherical arrangement of organic molecules in water solution clustered so that their hydrophobic parts are buried inside the sphere and their hydrophilic parts are on the surface of the sphere and in contact with water

  • momentum

    The product of the mass, m, and velocity, v, of an object. (Section 6.4)

  • Synstereoselective

    The addition of atoms or groups of atoms to the same face of a carbon-carbon double bond.

  • systematic name

    A name that is assigned using the rules of IUPAC nomenclature.

  • termination

    In radical reactions, a step in which two radicals are joined to give a compound with no unshared electrons.

  • valence bond theory

    A theory that treats a bond as the sharing of electrons that are associated with individual atoms, rather than being associated with the entire molecule.

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