Solutions for Chapter 5: Organic Chemistry 7th Edition

Organic Chemistry | 7th Edition | ISBN: 9781269406772 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9781269406772

Organic Chemistry | 7th Edition | ISBN: 9781269406772 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 5

Solutions for Chapter 5
4 5 0 258 Reviews
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Textbook: Organic Chemistry
Edition: 7
Author: Paula Yurkanis Bruice
ISBN: 9781269406772

Chapter 5 includes 81 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Organic Chemistry was written by Sieva Kozinsky and is associated to the ISBN: 9781269406772. Since 81 problems in chapter 5 have been answered, more than 89868 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • actinide series.

    Elements that have incompletely filled 5f subshells or readily give rise to cations that have incompletely filled 5f subshells. (7.9)

  • alpha particles

    Particles that are identical to helium-4 nuclei, consisting of two protons and two neutrons, symbol 4 2He or 4 2a. (Section 21.1)

  • amorphous solid

    A solid whose molecular arrangement lacks the regularly repeating long- range pattern of a crystal. (Section 12.2)

  • anomers

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

  • Arrhenius equation

    An equation that relates the rate constant for a reaction to the frequency factor, A, the activation energy, Ea, and the temperature, T: k = Ae-Ea>RT. In its logarithmic form it is written ln k = -Ea>RT + ln A. (Section 14.5)

  • base-dissociation constant (Kb)

    An equilibrium constant that expresses the extent to which a base reacts with solvent water, accepting a proton and forming OH-1aq2. (Section 16.7)

  • Condensation polymerization

    A polymerization in which chain growth occurs in a stepwise manner between difunctional monomers. Also called step-growth polymerization.

  • Deactivating group

    Any substituent on a benzene ring that causes the rate of electrophilic aromatic substitution to be lower than that for benzene.

  • Endothermic reaction

    A reaction in which the enthalpy of the products is higher than the enthalpy of the reactants; a reaction in which heat is absorbed

  • Formal charge

    The charge on an atom in a polyatomic ion or molecule

  • mass spectrometer

    A device inwhich a compound is first vaporized and convertedinto ions, which are then separated anddetected.

  • nanomaterial

    A solid whose dimensions range from 1 to 100 nm and whose properties differ from those of a bulk material with the same composition. (Section 12.1)

  • Oxidation

    The loss of electrons. Alternatively, either the loss of hydrogens, the gain of oxygens, or both.

  • phenoxide

    The conjugate base of phenol or a substituted phenol.

  • Plane-polarized light

    Light oscillating in only parallel planes.

  • polar molecule

    A molecule that possesses a nonzero dipole moment. (Section 8.4)

  • Primary structure of nucleic acids

    The sequence of bases along the pentose-phosphodiester backbone of a DNA or RNA molecule read from the 5’ end to the 3’ end

  • spin magnetic quantum number 1ms2

    A quantum number associated with the electron spin; it may have values of +12 or -12. (Section 6.7)

  • Steroid

    A plant or animal lipid having the characteristic tetracyclic ring structure of the steroid nucleus, namely three sixmembered rings and one fi ve-membered ring.

  • 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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