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Solutions for Chapter 4.17SE: 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 4.17SE

Solutions for Chapter 4.17SE
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Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Since 2 problems in chapter 4.17SE have been answered, more than 65296 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 4.17SE includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • anomers

    Stereoisomeric cyclic hemiacetals of an aldose or ketose that differ from each other in their configuration at the anomeric carbon.

  • antiaromatic

    Instability that arises when a planar ring of continuously overlapping p orbitals contains 4n p electrons.

  • 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)

  • carbohydrates

    Polyhydroxy aldehydes or ketones with molecular formula CxH2xOx.

  • deactivate

    For a substitutedaromatic ring, the effect of an electronwithdrawingsubstituent that decreases therate of electrophilic aromatic substitution.

  • diene

    A compound containing two carbon-carbon p bonds.

  • eicosanoids

    A class of lipids which includes leukotrienes, prostaglandins, thromboxanes, and prostacyclins.

  • 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.

  • Equivalent hydrogens

    Hydrogens that have the same chemical environment

  • fossil fuels

    Coal, oil, and natural gas, which are presently our major sources of energy. (Section 5.8)

  • hydride shift

    A type of carbocation rearrangement that involves the migration of a hydride ion (H-).

  • hydroxyl group

    An OH group.

  • n+1 rule

    In NMR spectroscopy, if n is the number of neighboring protons, then the multiplicity will be n+1.

  • optically pure

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

  • Orbital

    A region of space that can hold two electrons

  • ribonucleic acid (RNA)

    A polynucleotide in which ribose is the sugar component. (Section 24.10)

  • ring flip

    A conformational change in which one chair conformation is converted into the other.

  • saponification

    Hydrolysis of an ester in the presence of a base. (Section 24.4)

  • Staggered conformation

    A conformation about a carbon-carbon single bond in which the atoms or groups on one carbon are as far apart as possible from atoms or groups on an adjacent carbon.

  • Wavelength (l)

    The distance between consecutive peaks on a wave

Textbook Survival Guides

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