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Solutions for Chapter 14: Chemical Equilibrium

Chemistry: A Molecular Approach | 3rd Edition | ISBN: 9780321809247 | Authors: Nivaldo J. Tro

Full solutions for Chemistry: A Molecular Approach | 3rd Edition

ISBN: 9780321809247

Chemistry: A Molecular Approach | 3rd Edition | ISBN: 9780321809247 | Authors: Nivaldo J. Tro

Solutions for Chapter 14: Chemical Equilibrium

Solutions for Chapter 14
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Textbook: Chemistry: A Molecular Approach
Edition: 3
Author: Nivaldo J. Tro
ISBN: 9780321809247

This expansive textbook survival guide covers the following chapters and their solutions. Chapter 14: Chemical Equilibrium includes 104 full step-by-step solutions. Since 104 problems in chapter 14: Chemical Equilibrium have been answered, more than 443196 students have viewed full step-by-step solutions from this chapter. Chemistry: A Molecular Approach was written by and is associated to the ISBN: 9780321809247. This textbook survival guide was created for the textbook: Chemistry: A Molecular Approach, edition: 3.

Key Chemistry Terms and definitions covered in this textbook
  • aldehydes.

    Compounds with a carbonyl functional group and the general formula RCHO, where R is an H atom, an alkyl, or an aromatic group. (24.4)

  • alkene

    A compound that possesses a carbon-carbon double bond.

  • Avogadro’s law

    A statement that the volume of a gas maintained at constant temperature and pressure is directly proportional to the number of moles of the gas. (Section 10.3)

  • beta (b) position

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

  • breeder reactor.

    A nuclear reactor that produces more fissionable materials than it uses. (19.5)

  • buffer capacity

    The amount of acid or base a buffer can neutralize before the pH begins to change appreciably. (Section 17.2)

  • carbohydrates

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

  • coupling constant

    When signal splitting occurs in NMR spectroscopy, the distance between the individual peaks of a signal.

  • Crown ether

    A cyclic polyether derived from ethylene glycol and substituted ethylene glycols.

  • Dieckmann cyclization

    An intramolecular Claisen condensation.

  • face-centered lattice

    A crystal lattice in which the lattice points are located at the faces and corners of each unit cell. (Section 12.2)

  • hybrid orbital

    An orbital that results from the mixing of different kinds of atomic orbitals on the same atom. For example, an sp3 hybrid results from the mixing, or hybridizing, of one s orbital and three p orbitals. (Section 9.5)

  • Imine

    A compound containing a carbon-nitrogen double bond, R2C"NR’; also called a Schiff base

  • ionic reaction

    A reaction that involves the participation of ions as reactants, intermediates, or products.

  • Isoelectric point (pI)

    The pH at which an amino acid, polypeptide, or protein has no net charge

  • isoelectronic series

    A series of atoms, ions, or molecules having the same number of electrons. (Section 7.3)

  • lanthanide contraction

    The gradual decrease in atomic and ionic radii with increasing atomic number among the lanthanide elements, atomic numbers 57 through 70. The decrease arises because of a gradual increase in effective nuclear charge through the lanthanide series. (Section 23.1)

  • Lewis base

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

  • plane of symmetry

    A plane that bisects a compound into two halves that are mirror images of each other.

  • Reactive intermediate

    A high-energy species formed between two successive reaction steps, that lies in an energy minimum between the two transition states

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