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Solutions for Chapter 19: Chemistry: Atoms First 1st Edition

Chemistry: Atoms First | 1st Edition | ISBN: 9780073511160 | Authors: Julia Burdge, Jason Overby

Full solutions for Chemistry: Atoms First | 1st Edition

ISBN: 9780073511160

Chemistry: Atoms First | 1st Edition | ISBN: 9780073511160 | Authors: Julia Burdge, Jason Overby

Solutions for Chapter 19

Solutions for Chapter 19
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Textbook: Chemistry: Atoms First
Edition: 1
Author: Julia Burdge, Jason Overby
ISBN: 9780073511160

Chemistry: Atoms First was written by and is associated to the ISBN: 9780073511160. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Chemistry: Atoms First , edition: 1. Since 135 problems in chapter 19 have been answered, more than 89130 students have viewed full step-by-step solutions from this chapter. Chapter 19 includes 135 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • antibonding MO

    A high-energy molecular orbital resulting from the destructive interference between atomic orbitals.

  • aromatic hydrocarbon.

    A hydrocarbon that contains one or more benzene rings. (24.1)

  • Baeyer-Villiger oxidation

    A reaction in which a ketone is treated with a peroxy acid and is converted into an ester via the insertion of an oxygen atom.

  • Basicity

    An equilibrium property measured by the position of equilibrium in an acid-base reaction, as, for example, the acid-base reaction between ammonia and water.

  • Carboxylic ester

    A derivative of a carboxylic acid in which H of the carboxyl group is replaced by a carbon.

  • chemistry.

    The study of matter and the changes it undergoes. (1.1)

  • core electrons.

    All nonvalence electrons in an atom. (8.2)

  • double bond

    A covalent bond involving two electron pairs. (Section 8.3)

  • electrochemistry

    The branch of chemistry that deals with the relationships between electricity and chemical reactions. (Chapter 20: Introduction)

  • exo

    In Diels-Alder reactions that produce bicyclic structures, the positions that are anti to the larger bridge.

  • furanose

    A five-membered cyclic hemiacetal form of a carbohydrate.

  • node

    In atomic and molecular orbitals, a location where the value of y is zero.

  • optically pure

    A solution containing just one enantiomer, but not its mirror image.

  • racemic mixture

    A mixture of equal amounts of the dextrorotatory and levorotatory forms of a chiral molecule. A racemic mixture will not rotate the plane of polarized light. (Section 23.4)

  • retention of configuration

    During a reaction, when the configuration of a chirality center remains unchanged.

  • single bond

    A covalent bond involving one electron pair. (Section 8.3)

  • Solvolysis

    A nucleophilic substitution in which the solvent is also the nucleophile

  • Stork enamine synthesis

    A Michaelreaction in which an enamine functions as anucleophile.

  • Transfer RNA (tRNA

    A ribonucleic acid that carries a specifi c amino acid to the site of protein synthesis on ribosomes

  • trivalent

    An element, such as nitrogen, that forms three bonds.

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