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Solutions for Chapter 16.15SE: 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 16.15SE

Solutions for Chapter 16.15SE
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Since 2 problems in chapter 16.15SE have been answered, more than 67410 students have viewed full step-by-step solutions from this chapter. Chapter 16.15SE includes 2 full step-by-step solutions. 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. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • allylic bromination

    A radical reaction that achieves installation of a bromine atom at an allylic position.

  • Angle strain

    The strain that arises when a bond angle is either compressed or expanded compared to its optimal value.

  • 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

  • antibonding molecular orbital

    A molecular orbital in which electron density is concentrated outside the region between the two nuclei of bonded atoms. Such orbitals, designated as s* or p*, are less stable (of higher energy) than bonding molecular orbitals. (Section 9.7)

  • Aufbau principle

    Orbitals fi ll in order of increasing energy, from lowest to highest.

  • condensation reaction

    A chemical reaction in which a small molecule (such as a molecule of water) is split out from between two reacting molecules. (Sections 12.6 and 22.8)

  • Conjugated

    A conjugated diene or carbonyl is one in which the double bonds are separated by one single bond

  • diene

    A compound containing two carbon-carbon p bonds.

  • electron domain

    In the VSEPR model, a region about a central atom in which an electron pair is concentrated. (Section 9.2)

  • Hund’s rule

    A rule stating that electrons occupy degenerate orbitals in such a way as to maximize the number of electrons with the same spin. In other words, each orbital has one electron placed in it before pairing of electrons in orbitals occurs. (Section 6.8)

  • induction

    The withdrawal of electron density that occurs when a bond is shared by two atoms of differing electronegativity.

  • interhalogens

    Compounds formed between two different halogen elements. Examples include IBr and BrF3. (Section 22.4)

  • Molecular dipole moment (m)

    The vector sum of individual bond dipoles.

  • Oligosaccharide

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

  • primary structure

    The sequence of amino acids along a protein chain. (Section 24.7)

  • Prostaglandin

    A member of the family of compounds having the 20-carbon skeleton of prostanoic acid

  • radial probability function

    The probability that the electron will be found at a certain distance from the nucleus. (Section 6.6)

  • solvent

    The dissolving medium of a solution; it is normally the component of a solution present in the greater amount. (Section 4.1)

  • symmetrical ether

    An ether (R!O!R) where both R groups are identical.

  • Wavelength (l)

    The distance between consecutive peaks on a wave

Textbook Survival Guides

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