Solutions for Chapter 5.6SE: 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 5.6SE

Solutions for Chapter 5.6SE
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Since 2 problems in chapter 5.6SE have been answered, more than 123357 students have viewed full step-by-step solutions from this chapter. 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. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. Chapter 5.6SE includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • addition reactions

    Reactions that are characterized by the addition of two groups across a double bond. In the process, the pi (p) bond is broken.

  • aliphatic hydrocarbons.

    Hydrocarbons that do not contain the benzene group or the benzene ring. (24.1)

  • Antibonding molecular orbital

    A molecular orbital in which electrons have a higher energy than they would in isolated atomic orbitals

  • asymmetric hydrogenation

    The addition of H2 across only one face of a p bond.

  • Benzylic position

    An sp3 -hybridized carbon bonded to a benzene ring

  • Carboxylic ester

    A derivative of a carboxylic acid in which H of the carboxyl group is replaced by a carbon.

  • Chair conformation

    The most stable nonplanar conformation of a cyclohexane ring; all bond angles are approximately 109.5°, and all bonds on adjacent carbons are staggered.

  • complex lipid

    A lipid that readily undergoes hydrolysis in aqueous acid or base to produce smaller fragments.

  • covalent compounds.

    Compounds containing only covalent bonds. (9.4)

  • Crystalline domain

    An ordered crystalline region in the solid state of a polymer. Also called a crystallite.

  • Ether

    A compound containing an oxygen atom bonded to two carbon atoms.

  • face-centered lattice

    A crystal lattice in which the lattice points are located at the faces and corners of each unit cell. (Section 12.2)

  • fatty acids

    Long-chain carboxylic acids.

  • heat of fusion

    The enthalpy change, ?H, for melting a solid. (Section 11.4)

  • Heterocyclic amine

    An amine in which nitrogen is one of the atoms of a ring

  • hydrazone

    A compound with the structure R2CRN!NH2.

  • lambda max (lmax)

    In UVVis spectroscopy, the wavelength of maximum absorption.

  • precipitation reaction

    A reaction that occurs between substances in solution in which one of the products is insoluble. (Section 4.2)

  • rate equation

    An equation thatdescribes the relationship between the rate of a reactionand the concentration of reactants.

  • sterically hindered

    A compound or region of a compound that is very bulky.

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