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Solutions for Chapter 4.10SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Solutions for Chapter 4.10SE

Solutions for Chapter 4.10SE
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Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 4.10SE have been answered, more than 249982 students have viewed full step-by-step solutions from this chapter. Chapter 4.10SE includes 2 full step-by-step solutions. 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
  • 1,2-elimination

    An elimination reaction in which a proton from the beta (b) position is removed together with the leaving group, forming a double bond.

  • alkanes

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

  • alkyl halide

    An organic compound containing at least one halogen.

  • Bond length

    The distance between atoms in a covalent bond in picometers (pm; 1 pm 5 10212 m) or Å (1Å 5 10210 m).

  • conrotatory

    In electrocyclic reactions,a type of rotation in which the orbitals being used to form the new s bond must rotate in the same way.

  • critical temperature (Tc).

    The temperature above which a gas will not liquefy. (11.8)

  • deuterium

    The isotope of hydrogen whose nucleus contains a proton and a neutron: 2 1H. (Section 22.2)

  • exothermic

    Any process with a negative DH (the system gives energy to the surroundings).

  • High-resolution mass spectrometry

    Instrumentation that is capable of separating ions that differ in mass by as little as 0.0001 amu

  • levorotatory, or merely levo or l

    A term used to label a chiral molecule that rotates the plane of polarization of plane-polarized light to the left (counterclockwise). (Section 24.4)

  • micelle

    A group of molecules arranged in a sphere such that the surface of the sphere is comprised of polar groups, rendering the micelle water soluble.

  • Nucleophile

    From the Greek meaning nucleus-loving. Any species that can donate a pair of electrons to form a new covalent bond; alternatively, a Lewis base

  • optical isomerism

    A form of isomerism in which the two forms of a compound (stereoisomers) are nonsuperimposable mirror images. (Section 23.4)

  • optically active

    Possessing the ability to rotate the plane of polarized light. (Section 23.4)

  • osmosis

    The net movement of solvent through a semipermeable membrane toward the solution with greater solute concentration. (Section 13.5)

  • oxidation number (oxidation state)

    A positive or negative whole number assigned to an element in a molecule or ion on the basis of a set of formal rules; to some degree it reflects the positive or negative character of that atom. (Section 4.4)

  • oxyanion

    A polyatomic anion that contains one or more oxygen atoms. (Section 2.8)

  • rate-determining step

    The slowest elementary step in a reaction mechanism. (Section 14.6)

  • stereospecific

    A reaction in which the configuration of the product is dependent on the configuration of the starting material.

  • wedge

    In bond-line structures, a group in front of the page.

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