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Solutions for Chapter 23.1: NomeNclature 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 23.1: NomeNclature of amiNes

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. Since 8 problems in chapter 23.1: NomeNclature of amiNes have been answered, more than 36049 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by and is associated to the ISBN: 9781936221349. Chapter 23.1: NomeNclature of amiNes includes 8 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • addition polymerization

    Polymerization that occurs through coupling of monomers with one another, with no other products formed in the reaction. (Section 12.8)

  • atomic orbital

    A three-dimensional plot of y2 of a wavefunction. It is a region of space that can accommodate electron density.

  • carbohydrates

    A class of substances formed from polyhydroxy aldehydes or ketones. (Section 24.8)

  • concentration cell

    A voltaic cell containing the same electrolyte and the same electrode materials in both the anode and cathode compartments. The emf of the cell is derived from a difference in the concentrations of the same electrolyte solutions in the compartments. (Section 20.6)

  • covalent-network solids

    Solids in which the units that make up the three-dimensional network are joined by covalent bonds. (Section 12.1)

  • electrolytic cell

    A device in which a nonspontaneous oxidation–reduction reaction is caused to occur by passage of current under a sufficient external electrical potential. (Section 20.9)

  • Electromagnetic radiation

    Light and other forms of radiant energy.

  • free energy (Gibbs free energy, G)

    A thermodynamic state function that gives a criterion for spontaneous change in terms of enthalpy and entropy: G = H - TS. (Section 19.5)

  • gauche interaction

    The steric interaction that results when two groups in a Newman projection are separated by a dihedral angle of 60°.

  • greenhouse gases

    Gases in an atmosphere that absorb and emit infrared radiation (radiant heat), “trapping” heat in the atmosphere. (Section 18.2)

  • Hybridization

    The combination of atomic orbitals of different types

  • nuclear disintegration series

    A series of nuclear reactions that begins with an unstable nucleus and terminates with a stable one; also called a radioactive series. (Section 21.2)

  • ortho-para director

    A group that directs the regiochemistry of an electrophilic aromatic substitution reaction such that the incoming electrophile is installed at the ortho or para positions.

  • period

    The row of elements that lie in a horizontal row in the periodic table. (Section 2.5)

  • Prochiral hydrogens

    Refers to two hydrogens bonded to a carbon atom. When a different atom replaces one or the other, the carbon becomes a chiral center. The hydrogens of the CH2 group of ethanol, for example, are prochiral. Replacing one of them by deuterium gives (R)-1-deuteroethanol; replacing the other gives (S)-1-deuteroethanol

  • Shielding in NMR

    Also called diamagnetic shielding; the term refers to the reduction in magnetic fi eld strength experienced by a nucleus underneath electron density induced to circulate when the molecule is placed in a strong magnetic fi eld.

  • solvolysis

    A substitution reaction in which the solvent functions as the nucleophile.

  • sp3 Hybrid orbital

    A hybrid atomic orbital formed by the combination of one s atomic orbital and three 2p atomic orbitals.

  • tautomers

    Constitutional isomers that rapidly interconvert via the migration of a proton.

  • vinylic carbocation

    A carbocation in which the positive charge resides on a vinylic carbon atom. This type of carbocation is very unstable and will not readily form in most cases.

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