Solutions for Chapter 7.9 SE: 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 7.9 SE

Solutions for Chapter 7.9 SE
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Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 7.9 SE have been answered, more than 146002 students have viewed full step-by-step solutions from this chapter. Chapter 7.9 SE includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13.

Key Chemistry Terms and definitions covered in this textbook
  • absorbance

    In UV-Vis spectroscopy, the value log (I0/I) where I0 is the intensity of the reference beam and I is the intensity of the sample beam.

  • Acylium ion

    A resonance-stabilized cation with the structure [RC"O]1 or [ArC"O]1. The positive charge is delocalized over both the carbonyl carbon and the carbonyl oxygen.

  • capillary action

    The process by which a liquid rises in a tube because of a combination of adhesion to the walls of the tube and cohesion between liquid particles. (Section 11.3)

  • cathode.

    The electrode at which reduction occurs. (18.2)

  • chain reaction

    A series of reactions in which one reaction initiates the next. (Section 21.7)

  • chlorofluorocarbons

    Compounds composed entirely of chlorine, fluorine, and carbon. (Section 18.3)

  • condensed structure

    A drawing style in which none of the bonds are drawn. Groups of atoms are clustered together when possible. For example, isopropanol has two CH3 groups, both of which are connected to the central carbon atom, shown like this: (CH3)2CHOH.

  • coupling constant

    When signal splitting occurs in NMR spectroscopy, the distance between the individual peaks of a signal.

  • Fingerprint region

    Vibrations in the region 1500 to 400 cm21 of an IR spectrum are complex and diffi cult to analyze but are characteristic for different molecules.

  • Frost circle

    A graphic method for determining the relative energies of p MOs for planar, fully conjugated, monocyclic compounds.

  • Henderson-Hasselbalch equation

    An equation that is often employed to calculate the pH of buffered solutions: pH = pKa + log 3conjugated base4 3acid4

  • isoprene

    2-Methyl-1,3-butadiene.

  • ketone

    A compound in which the carbonyl group 1C “O2 occurs at the interior of a carbon chain and is therefore flanked by carbon atoms. (Section 24.4)

  • lambda max (lmax)

    In UVVis spectroscopy, the wavelength of maximum absorption.

  • Ortho

    Refers to groups occupying l,2-positions on a benzene ring.

  • plastic

    A material that can be formed into particular shapes by application of heat and pressure. (Section 12.8)

  • reducing sugar

    A carbohydrate that is oxidized upon treatment with Tollens’ reagent, Fehling’s reagent, or Benedict’s reagent.

  • Ring current

    An applied magnetic fi eld causes the p electrons of an aromatic ring to circulate, giving rise to the so-called ring current and an associated magnetic fi eld that opposes the applied fi eld in the middle of the ring but reinforces the applied fi eld on the outside of the ring.

  • second law of thermodynamics

    A statement of our experience that there is a direction to the way events occur in nature. When a process occurs spontaneously in one direction, it is nonspontaneous in the reverse direction. It is possible to state the second law in many different forms, but they all relate back to the same idea about spontaneity. One of the most common statements found in chemical contexts is that in any spontaneous process the entropy of the universe increases. (Section 19.2)

  • tautomers

    Constitutional isomers that rapidly interconvert via the migration of a proton.

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