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Solutions for Chapter 19.16: Hydrolysis of Nitriles

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 19.16: Hydrolysis of Nitriles

Solutions for Chapter 19.16
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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. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. Since 1 problems in chapter 19.16: Hydrolysis of Nitriles have been answered, more than 20542 students have viewed full step-by-step solutions from this chapter. Chapter 19.16: Hydrolysis of Nitriles includes 1 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Allylic carbocation

    A carbocation in which an allylic carbon bears the positive charge.

  • Angle strain

    The strain that arises when a bond angle is either compressed or expanded compared to its optimal value.

  • aryl amine

    An amine in which the nitrogen atom is connected directly to an aromatic ring.

  • base ionization constant (Kb).

    The equilibrium constant for the base ionization. (15.6)

  • becquerel

    The SI unit of radioactivity. It corresponds to one nuclear disintegration per second. (Section 21.4)

  • conjugate acid

    A substance formed by addition of a proton to a Brønsted–Lowry base. (Section 16.2)

  • crystallization

    The process in which molecules, ions, or atoms come together to form a crystalline solid. (Section 13.2)

  • Furanose

    A fi ve-membered cyclic form of a monosaccharide.

  • galvanic cell

    See voltaic cell. (Section 20.3)

  • Hess’s law

    The heat evolved in a given process can be expressed as the sum of the heats of several processes that, when added, yield the process of interest. (Section 5.6)

  • Heterocyclic aromatic amine

    An amine in which nitrogen is one of the atoms of an aromatic ring.

  • immiscible liquids

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

  • Lewis acid

    Any molecule or ion that can form a new covalent bond by accepting a pair of electrons.

  • nucleophilic acyl substitution

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

  • oxidation

    A reaction in which one compound undergoes an increase in oxidation state.

  • primary structure

    For proteins, the sequence of amino acid residues.

  • radical anion

    An intermediate that has both a negative charge and an unpaired electron.

  • redox (oxidation–reduction) reaction

    A reaction in which certain atoms undergo changes in oxidation states. The substance increasing in oxidation state is oxidized; the substance decreasing in oxidation state is reduced. (Section 4.4; Chapter 20: Introduction)

  • sterically hindered

    A compound or region of a compound that is very bulky.

  • sulfoxide

    A compound containing an SRO bond that is flanked on both sides by R groups.

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