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Solutions for Chapter 9.9SE: 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 9.9SE

Solutions for Chapter 9.9SE
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Chapter 9.9SE includes 2 full step-by-step solutions. Since 2 problems in chapter 9.9SE have been answered, more than 66600 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.

Key Chemistry Terms and definitions covered in this textbook
  • activation energy (Ea).

    The minimum amount of energy required to initiate a chemical reaction. (13.4)

  • Aldehyde

    A compound containing a !CHO group

  • alkanes.

    Hydrocarbons having the general formula CnH2n12, where n 5 1,2, . . . . (24.2)

  • amphiprotic

    Refers to the capacity of a substance to either add or lose a proton 1H+2. (Section 16.2)

  • anode

    An electrode at which oxidation occurs. (Section 20.3)

  • 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

  • beta sheet

    A structural form of protein in which two strands of amino acids are hydrogen-bonded together in a zipperlike configuration. (Section 24.7)

  • calorie

    A unit of energy; it is the amount of energy needed to raise the temperature of 1 g of water by 1 °C from 14.5 °C to 15.5 °C. A related unit is the joule: 1 cal = 4.184 J. (Section 5.1)

  • Carbene

    A neutral molecule that contains a carbon atom surrounded by only six valence electrons (R2C:).

  • chain reaction

    A reaction (generally involving radicals) in which one chemical entity can ultimately cause a chemical transformation for thousands of molecules.

  • conjugate addition

    An addition reaction in which a nucleophile and a proton are added across the two ends of a conjugated p system.

  • Diaxial interactions

    Refers to the steric strain arising from interaction between an axial substituent and an axial hydrogen (or other group) on the same side of a chair conformation of a cyclohexane ring

  • enantiomeric excess

    For a mixture containing two enantiomers, the difference between the percent concentration of the major enantiomer and the percent concentration of its mirror image.

  • Lewis dot structure

    The symbol of an element surrounded by a number of dots equal to the number of electrons in the valence shell of the atom

  • nuclear model

    Model of the atom with a nucleus containing protons and neutrons and with electrons in the space outside the nucleus. (Section 2.2)

  • phenoxide

    The conjugate base of phenol or a substituted phenol.

  • quaternary structure

    The structure that arises when a protein consists of two or more folded polypeptide chains that aggregate to form one protein complex.

  • racemic mixture

    A solution containing equal amounts of both enantiomers.

  • sulfide

    A compound that is similar in structure to an ether, but the oxygen atom has been replaced with a sulfur atom. Also called a thioether.

  • three-center, two-electron bonds

    A bond in which two electrons are associated with three atoms, such as in diborane (B2H6).

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