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Solutions for Chapter 4.4: An Asymmetric Center is a Cause of Chirality in a Molecule

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 8th Edition

ISBN: 9780134042282

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 4.4: An Asymmetric Center is a Cause of Chirality in a Molecule

Solutions for Chapter 4.4
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This expansive textbook survival guide covers the following chapters and their solutions. Chapter 4.4: An Asymmetric Center is a Cause of Chirality in a Molecule includes 2 full step-by-step solutions. Since 2 problems in chapter 4.4: An Asymmetric Center is a Cause of Chirality in a Molecule have been answered, more than 31133 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. Organic Chemistry was written by and is associated to the ISBN: 9780134042282.

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)

  • alkenes

    Hydrocarbons containing one or more carbon–carbon double bonds. (Section 24.2)

  • allylic carbocation

    A carbocation in which the positive charge is adjacent to a carbon-carbon double bond.

  • Benzyne intermediate

    A reactive intermediate formed by b-elimination from adjacent carbon atoms of a benzene ring and having a triple bond in the benzene ring. The second p bond of the benzyne triple bond is formed by the weak overlap of coplanar 2p orbitals on adjacent carbons.

  • blocking group

    A group that can be readily installed and uninstalled. Used for regiochemical control during synthesis.

  • complex ion (complex)

    An assembly of a metal ion and the Lewis bases (ligands) bonded to it. (Section 17.5)

  • constitutional isomers

    Compounds that have the same molecular formula but differ in the way the atoms are connected.

  • delocalized

    A lone pair or charge that is participating in resonance.

  • dipole

    A molecule with one end having a partial negative charge and the other end having a partial positive charge; a polar molecule. (Section 8.4)

  • electrophile

    A compound containing an electron-deficient atom that is capable of accepting a pair of electrons.

  • entropy

    The measure of disorder associated with a system.

  • Faraday constant (F )

    The magnitude of charge of one mole of electrons: 96,500 C>mol. (Section 20.5)

  • homogeneous catalysts

    A catalyst that dissolves in the reaction medium.

  • hydrogen bonding

    Bonding that results from intermolecular attractions between molecules containing hydrogen bonded to an electronegative element. The most important examples involve OH, NH, and HF. (Section 11.2)

  • isoelectronic series

    A series of atoms, ions, or molecules having the same number of electrons. (Section 7.3)

  • Lewis symbol (electron-dot symbol)

    The chemical symbol for an element, with a dot for each valence electron. (Section 8.1)

  • meso compound

    A compound that possesses chirality centers and an internal plane of symmetry.

  • photoelectric effect

    The emission of electrons from a metal surface induced by light. (Section 6.2)

  • retrosynthetic analysis

    A systematic set of principles that enable the design of a synthetic route by working backward from the desired product.

  • Wavenumbers (—n )

    The frequency of electromagnetic radiation expressed as the number of waves per centimeter, with units cm21 (read: reciprocal centimeters).

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