Solutions for Chapter 3.9SE: 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 3.9SE

Solutions for Chapter 3.9SE
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Since 2 problems in chapter 3.9SE have been answered, more than 148268 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Chapter 3.9SE includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • activity series.

    A summary of the results of many possible displacement reactions. (4.4)

  • Aldehyde

    A compound containing a !CHO group

  • amphoteric oxides and hydroxides

    Oxides and hydroxides that are only slightly soluble in water but that dissolve in either acidic or basic solutions. (Section 17.5)

  • Aprotic acid

    An acid that is not a proton donor; an acid that is an electron pair acceptor in a Lewis acid-base reaction.

  • Autoxidation

    Air oxidation of materials such as unsaturated fatty acids.

  • catalyst.

    A substance that increases the rate of a chemical reaction without itself being consumed. (13.6)

  • curie

    A measure of radioactivity: 1 curie = 3.7 * 1010 nuclear disintegrations per second. (Section 21.4)

  • Downfield

    A signal of an NMR spectrum that is shifted toward the left (larger chemical shift) on the chart paper.

  • Glycosidic bond

    The bond from the anomeric carbon of a glycoside to an !OR group

  • Ground state

    The lowest energy state of a system.

  • haloform reaction

    A reaction in which a methyl ketone is converted into a carboxylic acid upon treatment with excess base and excess halogen, followed by aqueous acid.

  • internal energy

    The total energy possessed by a system. When a system undergoes a change, the change in internal energy, ?E, is defined as the heat, q, added to the system, plus the work, w, done on the system by its surroundings: ?E = q + w. (Section 5.2)

  • leveling effect

    An effect thatprevents the use of bases stronger than hydroxidewhen the solvent is water.

  • Lewis base

    A compound capable offunctioning as an electron pair donor.

  • Monomer

    From the Greek, mono 1 meros, meaning single part. The simplest nonredundant unit from which a polymer is synthesized.

  • Nucleic acid

    A biopolymer containing three types of monomer units: heterocyclic aromatic amine bases derived from purine and pyrimidine, the monosaccharides d-ribose or 2-deoxy-d-ribose, and phosphoric acid

  • oxymercuration-demercuration

    A two-step process for the Markovnikov addition of water across an alkene. With this process, carbocation rearrangements do not occur.

  • Pyranose

    A six-membered cyclic form of a monosaccharide.

  • Resonance hybrid

    A molecule, ion, or radical described as a composite of a number of contributing structures

  • Stereospecific reaction

    A special type of stereoselective reaction in which the stereochemistry of the product is dependent on the stereochemistry of the starting material.

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