Solutions for Chapter 24.7SE: 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 24.7SE

Solutions for Chapter 24.7SE
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Chapter 24.7SE includes 2 full step-by-step solutions. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 24.7SE have been answered, more than 141460 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • addition polymerization

    Polymerization that occurs through coupling of monomers with one another, with no other products formed in the reaction. (Section 12.8)

  • Alditol

    The product formed when the C"O group of a monosaccharide is reduced to a CHOH group.

  • alkyl amines

    A format for naming amines containing simple alkyl groups.

  • Antiaromatic compound

    A monocyclic compound that is planar or nearly so, has one 2p orbital on each atom of the ring, and has 4n p electrons in the cyclic arrangement of overlapping 2p orbitals, where n is an integer. Antiaromatic compounds are especially unstable

  • antioxidants

    Radical scavengers that prevent autooxidation by preventing radical chain reactions from beginning.

  • Atactic polymer

    A polymer with completely random confi gurations at the chiral centers along its chain, as, for example, atactic polypropylene

  • breeder reactor.

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

  • Brønsted-Lowry acid

    A compound that can serve as a proton donor.

  • copolymer.

    A polymer containing two or more different monomers. (25.2)

  • Cycloaddition reaction

    A reaction in which two reactants add together in a single step to form a cyclic product. The best known of these is the Diels-Alder reaction

  • dehydrohalogenation

    An elimination reaction involving the loss of H and a halogen (such as Cl, Br, or I).

  • diastereotopic

    Nonequivalent protons for which the replacement test produces diastereomers.

  • ester

    An organic compound that has an OR group attached to a carbonyl; it is the product of a reaction between a carboxylic acid and an alcohol. (Section 24.4)

  • interhalogens

    Compounds formed between two different halogen elements. Examples include IBr and BrF3. (Section 22.4)

  • nucleotide

    Compounds formed from a molecule of phosphoric acid, a sugar molecule, and an organic nitrogen base. Nucleotides form linear polymers called DNA and RNA, which are involved in protein synthesis and cell reproduction. (Section 24.10)

  • polarimeter

    A device that measures the rotation of plane-polarized light caused by optically active compounds.

  • property

    A characteristic that gives a sample of matter its unique identity. (Section 1.1)

  • secondary cell

    A voltaic cell that can be recharged. (Section 20.7)

  • Triglyceride (triacylglycerol)

    An ester of glycerol with three fatty acids

  • Wolff-Kishner reduction

    A method for converting a carbonyl group into a methylene group (CH2) under basic conditions.

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