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Solutions for Chapter 3.11: Some Cycloalkanes Have Angle Strain

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9780321803221

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 3.11: Some Cycloalkanes Have Angle Strain

Chapter 3.11: Some Cycloalkanes Have Angle Strain includes 3 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. This expansive textbook survival guide covers the following chapters and their solutions. Since 3 problems in chapter 3.11: Some Cycloalkanes Have Angle Strain have been answered, more than 32787 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by and is associated to the ISBN: 9780321803221.

Key Chemistry Terms and definitions covered in this textbook
  • Aufbau principle.

    As protons are added one by one to the nucleus to build up the elements, electrons similarly are added to the atomic orbitals. (7.9)

  • bond cleavage

    The breaking of a bond, either homolytically or heterolytically. bond dissociation energy (Sect. 6.1): The energy required to achieve homolytic bond cleavage (generating radicals).

  • chelating agent.

    A substance that forms complex ions with metal ions in solution. (23.3)

  • chemical properties

    Properties that describe a substance’s composition and its reactivity; how the substance reacts or changes into other substances. (Section 1.3)

  • conjugate base

    In an acid-base reaction, the product that results when an acid is deprotonated.

  • Deactivating group

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

  • dilution

    The process of preparing a less concentrated solution from a more concentrated one by adding solvent. (Section 4.5)

  • electrophilic aromatic substitution

    A substitution reaction in which an aromatic proton is replaced by an electrophile and the aromatic moiety is preserved.

  • 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.

  • glass transition temperature (Tg)

    The temperature at which noncrystalline polymers become very soft.

  • Heterolytic bond cleavage

    Cleavage of a bond so that one fragment retains both electrons and the other retains none.

  • hydrocarbons

    Compounds composed of only carbon and hydrogen. (Section 2.9)

  • molecularity

    The number of molecules that participate as reactants in an elementary reaction. (Section 14.6)

  • phenyl group

    A C6H5 group.

  • Regioselective reaction

    An addition or substitution reaction in which one of two or more possible products is formed in preference to all others that might be formed.

  • representative (main-group) element

    An element from within the s and p blocks of the periodic table (Figure 6.29). (Section 6.9)

  • 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.

  • thiols

    Compounds containing a mercapto group (SH).

  • Transition state

    The highest energy point on a reaction coordinate diagram. The chemical structure at this point is commonly called an activated complex.

  • twist boat

    A conformation of cyclohexane that is lower in energy than a boat conformation but higher in energy than a chair conformation.

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