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Solutions for Chapter 14.9SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

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

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Solutions for Chapter 14.9SE

Solutions for Chapter 14.9SE
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Chapter 14.9SE includes 2 full step-by-step solutions. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. 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. Since 2 problems in chapter 14.9SE have been answered, more than 245478 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • Alkyl group

    A group derived by removing a hydrogen from an alkane; given the symbol R!

  • Amino acid

    A compound that contains both an amino group and a carboxyl group

  • annulenes

    Compounds consisting of a single ring containing a fully conjugated p system. Benzene is [6]annulene.

  • bond-line structures

    The most common drawing style employed by organic chemists. All carbon atoms and most hydrogen atoms are implied but not explicitly drawn in a bond-line structure.

  • breeder reactor.

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

  • Conjugate base

    The species formed when an acid transfers a proton to a base

  • Correlation tables

    Tables of data on absorption patterns of functional groups.

  • Cumulated

    A cumulated diene is one in which two double bonds share an sp-hybridized carbon

  • Double-headed arrow

    A symbol used to show that structures on either side of it are resonance-contributing structures

  • electron density

    The probability of finding an electron at any particular point in an atom; this probability is equal to c2, the square of the wave function. Also called the probability density. (Section 6.5)

  • Hofmann elimination

    When treated with a strong base, a quaternary ammonium halide undergoes b-elimination by an E2 mechanism to give the less-substituted alkene as the major product

  • Index of hydrogen defi ciency

    The sum of the number of rings and p bonds in a molecule.

  • Newman projection

    A drawing style that is designed to show the conformation of a molecule.

  • Polyester

    A polymer in which each monomer unit is joined to the next by an ester bond, as, for example, poly(ethylene terephthalate).

  • R

    A term used to designate the configuration of a chirality center, determined in the following way: Each of the four groups is assigned a priority, and the molecule is then rotated (if necessary) so that the #4 group is directed behind the page (on a dash). A clockwise sequence for 1-2-3 is designated as R.

  • rare earth element

    See lanthanide element. (Sections 6.8 and 6.9)

  • Reduction

    The gain of electrons. Alternatively, either the gain of hydrogen, loss of oxygen, or both

  • syn-coplanar

    A conformation in which a hydrogen atom and a leaving group are separated by a dihedral angle of exactly 0°.

  • torsional angle

    The angle between two groups in a Newman projection, also called the dihedral angle.

  • Wohl degradation

    A process that involves the removal of a carbon atom from an aldose. The aldehyde group is first converted to a cyanohydrin, followed by loss of HCN in the presence of a base.

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