Solutions for Chapter 16.10SE: 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 16.10SE

Solutions for Chapter 16.10SE
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Chapter 16.10SE includes 2 full step-by-step solutions. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 16.10SE have been answered, more than 147630 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.

Key Chemistry Terms and definitions covered in this textbook
  • alkanes

    Compounds of carbon and hydrogen containing only carbon–carbon single bonds. (Sections 2.9 and 24.2)

  • Alkene metathesis

    A reaction in which two alkenes interchange the carbons attached to their double bonds.

  • azo coupling

    An electrophilic aromatic substitution reaction in which an aryldiazonium salt reacts with an activated aromatic ring.

  • battery

    A self-contained electrochemical power source that contains one or more voltaic cells. (Section 20.7)

  • Chain termination

    A step in a chain reaction that involves destruction of reactive intermediates

  • Cyanohydrin

    A molecule containing an !OH group and a !CN group bonded to the same carbon.

  • elastomer

    A material that can undergo a substantial change in shape via stretching, bending, or compression and return to its original shape upon release of the distorting force. (Section 12.6)

  • electronic charge

    The negative charge carried by an electron; it has a magnitude of 1.602 * 10-19 C. (Section 2.3)

  • f-block metals

    Lanthanide and actinide elements in which the 4f or 5f orbitals are partially occupied. (Section 6.9)

  • Gibbs free energy (G)

    The ultimate arbiter of the spontaneity of a reaction, where DG = DH - T DS.

  • Glycol

    A compound with hydroxyl (!OH) groups on adjacent carbons.

  • Inductive effect

    The polarization of the electron density of a covalent bond caused by the electronegativity of a nearby atom.

  • lambda max (lmax)

    In UVVis spectroscopy, the wavelength of maximum absorption.

  • 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

  • Node

    A point in space where the value of a wave function is zero

  • observed rotation

    The extent to which plane-polarized light is rotated by a solution of a chiral compound.

  • Oligosaccharide

    A carbohydrate containing four to ten monosaccharide units, each joined to the next by a glycosidic bond.

  • optically inactive

    A compound that does not rotate plane-polarized light.

  • substitution reactions

    Reactions in which one group is replaced by another group.

  • Vinyl group

    A carbocation in which the positive charge is on one of the carbons of a carbon-carbon double bond.

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