Solutions for Chapter 21.9: Preparation of Amines by Reduction

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 21.9: Preparation of Amines by Reduction

Solutions for Chapter 21.9
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Since 1 problems in chapter 21.9: Preparation of Amines by Reduction have been answered, more than 12684 students have viewed full step-by-step solutions from this chapter. Chapter 21.9: Preparation of Amines by Reduction includes 1 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9.

Key Chemistry Terms and definitions covered in this textbook
  • Alkene metathesis

    A reaction in which two alkenes interchange the carbons attached to their double bonds.

  • Bicycloalkane

    An alkane containing two rings that share two carbons

  • bond angles

    The angles made by the lines joining the nuclei of the atoms in a molecule. (Section 9.1)

  • cation

    A structure that bears a positive charge.

  • chemical equation.

    An equation that uses chemical symbols to show what happens during a chemical reaction. (3.7)

  • diazotization

    The process of forming a diazonium salt by treating a primary amine with NaNO2 and HCl.

  • double helix

    The structure for DNA that involves the winding of two DNA polynucleotide chains together in a helical arrangement. The two strands of the double helix are complementary in that the organic bases on the two strands are paired for optimal hydrogen bond interaction. (Section 24.10)

  • doublet

    In NMR spectroscopy, a signal that is comprised of two peaks.

  • effusion

    The escape of a gas through an orifice or hole. (Section 10.8)

  • enantiomer

    A nonsuperimposable mirror image.

  • Heterolytic bond cleavage

    Cleavage of a bond so that one fragment retains both electrons and the other retains none.

  • intermolecular forces

    The attractive forces between molecules.

  • Mass spectrometry

    An analytical technique for measuring the mass-to-charge ratio (m/z) of ions.

  • normal melting point

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

  • pressure–volume (PV) work

    Work performed by expansion of a gas against a resisting pressure. (Section 5.3)

  • radioisotope

    An isotope that is radioactive; that is, it is undergoing nuclear changes with emission of radiation. (Section 21.1)

  • reaction mechanism

    A series of intermediates and curved arrows that show howthe reaction occurs in terms of the motion of electrons.

  • SN2 reaction

    A bimolecular nucleophilic substitution reaction.

  • 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.

  • Zwitterion

    An internal salt of an amino acid; the carboxylate is negatively charged, and the ammonium group is positively charged

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