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Solutions for Chapter 16.4SE: 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 16.4SE

Solutions for Chapter 16.4SE
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Chapter 16.4SE includes 2 full step-by-step solutions. Since 2 problems in chapter 16.4SE have been answered, more than 66529 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. 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
  • active site

    Specific site on a heterogeneous catalyst or an enzyme where catalysis occurs. (Section 14.7)

  • autoionization

    The process whereby water spontaneously forms low concentrations of H+1aq2 and OH-1aq2 ions by proton transfer from one water molecule to another. (Section 16.3)

  • Autoxidation

    Air oxidation of materials such as unsaturated fatty acids.

  • 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.

  • chemical kinetics

    The area of chemistry concerned with the speeds, or rates, at which chemical reactions occur. (Chapter 14: Introduction)

  • Cycloalkane

    A saturated hydrocarbon that contains carbons joined to form a ring

  • E,Z system

    A system to specify the confi guration of groups about a carbon-carbon double bond

  • enthalpy of formation

    The enthalpy change that accompanies the formation of a substance from the most stable forms of its component elements. (Section 5.7)

  • epoxide

    A cyclic ether containing a three-membered ring system. Also called an oxirane (also see Sect. 14.7).

  • equatorial position

    For chair conformations of substituted cyclohexanes, a position that is approximately along the equator of the ring.

  • heat capacity

    The quantity of heat required to raise the temperature of a sample of matter by 1 °C (or 1 K). (Section 5.5)

  • heat of combustion

    The heat given off during a reaction in which an alkane reacts with oxygen to produce CO2 and water.

  • irreversible process

    A process that cannot be reversed to restore both the system and its surroundings to their original states. Any spontaneous process is irreversible. (Section 19.1)

  • Isotactic polymer

    A polymer with identical confi gurations (either all R or all S) at all chiral centers along its chain, as, for example, isotactic polypropylene

  • main-group elements

    Elements in the s and p blocks of the periodic table. (Section 6.9)

  • Observed rotation

    the number of degrees through which a compound rotates the plane of polarized light

  • optically pure

    A solution containing just one enantiomer, but not its mirror image.

  • resonance structures (resonance forms)

    Individual Lewis structures in cases where two or more Lewis structures are equally good descriptions of a single molecule. The resonance structures in such an instance are “averaged” to give a more accurate description of the real molecule. (Section 8.6)

  • steric number

    The total of (single bonds + lone pairs) for an atom in a compound.

  • Syndiotactic polymer

    A polymer with alternating R and S confi gurations at the chiral centers along its chain, as, for example, syndiotactic polypropylene

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