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Solutions for Chapter 14.15SE: 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 14.15SE

Solutions for Chapter 14.15SE
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Since 2 problems in chapter 14.15SE have been answered, more than 68022 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. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. Chapter 14.15SE includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • aldol addition reaction

    A reaction that occurs when an aldehyde or ketone is attacked by an enolate ion. The product of an aldol addition reaction is always a b-hydroxy aldehyde or ketone.

  • Anomers

    Carbohydrates that differ in confi guration only at their anomeric carbons.

  • beta elimination

    An elimination reaction in which a proton from the beta (b) position is removed together with the leaving group, forming a double bond.

  • cathodic protection

    A means of protecting a metal against corrosion by making it the cathode in a voltaic cell. This can be achieved by attaching a more easily oxidized metal, which serves as an anode, to the metal to be protected. (Section 20.8)

  • closest packing.

    The most efficient arrangements for packing atoms, molecules, or ions in a crystal. (11.4)

  • combustion reaction.

    A reaction in which a substance reacts with oxygen, usually with the release of heat and light, to produce a flame. (4.4)

  • Decarboxylation

    Loss of CO2 from a carboxyl group.

  • delocalized molecular orbitals.

    Molecular orbitals that are not confined between two adjacent bonding atoms but actually extend over three or more atoms. (10.8)

  • diene

    A compound containing two carbon-carbon p bonds.

  • hydrogen bonding

    Bonding that results from intermolecular attractions between molecules containing hydrogen bonded to an electronegative element. The most important examples involve OH, NH, and HF. (Section 11.2)

  • intermolecular forces

    The attractive forces between molecules.

  • Monomer

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

  • plane-polarized light

    Light for which all photons have the same polarization, generally formed by passing light through a polarizing filter.

  • Racemic mixture

    A mixture of equal amounts of two enantiomers.

  • Rate determining step

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

  • Resolution

    Separation of a racemic mixture into its enantiomers; in mass spectrometry, a measure of how well a mass spectrometer separates ions of different mass.

  • Sigma (s) molecular orbital

    A molecular orbital in which electron density is concentrated between two nuclei, along the axis joining them, and is cylindrically symmetrical

  • Staggered conformation

    A conformation about a carbon-carbon single bond in which the atoms or groups on one carbon are as far apart as possible from atoms or groups on an adjacent carbon.

  • third order

    A reaction that has a rate equation in which the sum of all exponents is three

  • Wavenumbers (—n )

    The frequency of electromagnetic radiation expressed as the number of waves per centimeter, with units cm21 (read: reciprocal centimeters).

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