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Solutions for Chapter 18: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Solutions for Chapter 18

Solutions for Chapter 18
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Textbook: Chemistry: The Central Science
Edition: 13
Author: Theodore E. Brown
ISBN: 9780321910417

Chapter 18 includes 206 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. Since 206 problems in chapter 18 have been answered, more than 68176 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Allene

    The compound CH2"C"CH2. Any compound that contains adjacent carbon-carbon double bonds; that is, any molecule that contains a C"C"C functional group.

  • 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)

  • autocatalytic

    A reaction for which the reagent necessary to catalyze the reaction is produced by the reaction itself.

  • Benzyl group (C6H5CH2!)

    The group derived from toluene by removing a hydrogen from its methyl group.

  • Chain initiation

    A step in a chain reaction characterized by the formation of reactive intermediates (radicals, anions, or cations) from nonradical or noncharged molecules

  • enantiomerically pure

    A substance that consists of a single enantiomer, and not its mirror image.

  • Entropy (S)

    Measures chaos versus order and chaos is favorable

  • halohydrin formation

    A reaction which involves the addition of a halogen and a hydroxyl group (OH) across an alkene.

  • keto-enol tautomerization

    The equilibrium that is established between an enol and a ketone in either acid-catalyzed or basecatalyzed conditions.

  • l-Monosaccharide

    A monosaccharide that, when written as a Fischer projection, has the !OH on its penultimate carbon to the left.

  • nonionizing radiation

    Radiation that does not have sufficient energy to remove an electron from a molecule. (Section 21.9)

  • photoelectric effect

    The emission of electrons from a metal surface induced by light. (Section 6.2)

  • plastic

    A material that can be formed into particular shapes by application of heat and pressure. (Section 12.8)

  • Polypeptide

    A macromolecule containing many amino acid units, each joined to the next by a peptide bond

  • Rate determining step

    The step in a multistep reaction sequence that crosses the highest energy barrier.

  • Telechelic polymer

    A polymer in which its growing chains are terminated by formation of new functional groups at both ends of its chains. These new functional groups are introduced by adding reagents, such as CO2 or ethylene oxide, to the growing chains.

  • terminal alkynes

    Compounds with the following structure: R!C#C!H

  • thermoplastics

    Polymers that are hard at room temperature but soft when heated.

  • wavelength

    The distance between adjacent peaks of an oscillating magnetic or electric field.

  • Zaitsev’s rule

    A rule stating that the major product of a b-elimination reaction is the most stable alkene; that is, it is the alkene with the greatest number of substituents on the carboncarbon double bond

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