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Solutions for Chapter 19: Nuclear Chemistry

Chemistry | 12th Edition | ISBN: 9780078021510 | Authors: Jerrold E. Marsden

Full solutions for Chemistry | 12th Edition

ISBN: 9780078021510

Chemistry | 12th Edition | ISBN: 9780078021510 | Authors: Jerrold E. Marsden

Solutions for Chapter 19: Nuclear Chemistry

Solutions for Chapter 19
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Textbook: Chemistry
Edition: 12
Author: Jerrold E. Marsden
ISBN: 9780078021510

Chemistry was written by and is associated to the ISBN: 9780078021510. Since 110 problems in chapter 19: Nuclear Chemistry have been answered, more than 11652 students have viewed full step-by-step solutions from this chapter. Chapter 19: Nuclear Chemistry includes 110 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry, edition: 12. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • 1,4-addition

    A reaction involving the addition of two groups to a conjugated p system in which one group is installed at the C1 position and the other group is installed at the C4 position.

  • addition to p bond

    One of the six kinds of arrow-pushing patterns used in drawing mechanisms for radical reactions. A radical adds to a p bond, destroying the p bond and generating a new radical.

  • Aliphatic amine

    An amine in which nitrogen is bonded only to alkyl groups.

  • amino acid

    A carboxylic acid that contains an amino 1¬NH22 group attached to the carbon atom adjacent to the carboxylic acid 1¬COOH2 functional group. (Section 24.7)

  • chain branching

    During polymerization, the growth of a branch connected to the main chain.

  • Chain propagation

    A step in a chain reaction characterized by the reaction of a reactive intermediate and a molecule to give a new reactive intermediate and a new molecule.

  • chemistry

    The scientific discipline that studies the composition, properties, and transformations of matter. (Chapter 1: Introduction)

  • Claisen condensation

    A nucleophilic acyl substitution reaction in which the nucleophile is an ester enolate and the electrophile is an ester.

  • Condensation polymerization

    A polymerization in which chain growth occurs in a stepwise manner between difunctional monomers. Also called step-growth polymerization.

  • dispersion forces

    Intermolecular forces resulting from attractions between induced dipoles. Also called London dispersion forces. (Section 11.2)

  • functional group

    An atom or group of atoms that imparts characteristic chemical properties to an organic compound. (Section 24.1)

  • Ground state

    The lowest energy state of a system.

  • lipid bilayer

    The main fabricof cell membranes, assembled primarily fromphosphoglycerides.

  • Meta (m)

    Refers to groups occupying 1,3-positions on a benzene ring.

  • Planck constant (h)

    The constant that relates the energy and frequency of a photon, E = hn. Its value is 6.626 * 10-34 J@s. (Section 6.2)

  • Raoult’s law

    A law stating that the partial pressure of a solvent over a solution, Psolution, is given by the vapor pressure of the pure solvent, P° solvent, times the mole fraction of a solvent in the solution, Xsolvent: Psolution = XsolventP° solvent. (Section 13.5)

  • Sharpless asymmetric epoxidation

    A reaction that converts an alkene into an epoxide via a stereospecific pathway.

  • step-growth polymers

    Polymers that are formed under conditions in which the individual monomers react with each other to form oligomers, which are then joined together to form polymers.

  • tetrahedral

    The geometry of an atom with four bonds separated from each other by 109.5°.

  • VSEPR theory

    Valence Shell Electron Pair Repulsion theory, which can be used to predict the geometry around an atom.

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