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Solutions for Chapter 17.4SE: 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 17.4SE

Solutions for Chapter 17.4SE
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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. Since 2 problems in chapter 17.4SE have been answered, more than 66522 students have viewed full step-by-step solutions from this chapter. Chapter 17.4SE includes 2 full step-by-step solutions. 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
  • amphoteric

    Compounds that will react with either acids or bases. Amino acids are amphoteric.

  • antiaromatic

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

  • antibonding molecular orbital.

    A molecular orbital that is of higher energy and lower stability than the atomic orbitals from which it was formed. (10.6)

  • bridgeheads

    In a bicyclic system, the carbon atoms where the rings are fused together.

  • conformation

    A three-dimensional shape that can be adopted by a compound as a result of rotation about single bonds.

  • denaturation

    A process during which a protein unfolds under conditions of mild heating.

  • E1cb mechanism

    An eliminationreaction in which the leaving group only leavesafter deprotonation occurs. This process occurs atthe end of an aldol condensation.

  • Electromagnetic radiation

    Light and other forms of radiant energy.

  • excited state

    A higher energy state than the ground state. (Section 6.3)

  • Fourier-transform NMR (FT-NMR)

    In nuclear magnetic resonance (NMR) spectroscopy, a technique in which the sample is irradiated with a short pulse that covers the entire range of relevant rf frequencies.

  • homogeneous equilibrium

    The equilibrium established between reactant and product substances that are all in the same phase. (Section 15.4)

  • methyl shift

    A type of carbocation rearrangement in which a methyl group migrates.

  • off-resonance decoupling

    In NMR spectroscopy, a technique in which only the one-bond couplings are observed. CH3 groups appear as quartets, CH2 groups appear as triplets, CH groups appear as doublets, and quaternary carbon atoms appear as singlets.

  • overlap

    The extent to which atomic orbitals on different atoms share the same region of space. When the overlap between two orbitals is large, a strong bond may be formed. (Section 9.4)

  • prostaglandins

    Lipids that contain 20 carbon atoms and are characterized by a five-membered ring with two side chains.

  • radial probability function

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

  • Radical

    Any chemical species that contains one or more unpaired electrons.

  • reverse osmosis

    The process by which water molecules move under high pressure through a semipermeable membrane from the more concentrated to the less concentrated solution. (Section 18.4)

  • Stereoisomers

    Isomers that have the same molecular formula and the same connectivity of their atoms but a different orientation of their atoms in space

  • substituents

    In nomenclature, the groups connected to the parent chain.

Textbook Survival Guides

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