Solutions for Chapter 6.4: Electrophilic Addition of Hydrogen Halides to Alkenes

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 6.4: Electrophilic Addition of Hydrogen Halides to Alkenes

Solutions for Chapter 6.4
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This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. Chapter 6.4: Electrophilic Addition of Hydrogen Halides to Alkenes includes 2 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 6.4: Electrophilic Addition of Hydrogen Halides to Alkenes have been answered, more than 11000 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • alternating copolymers

    A copolymer that contains an alternating distribution of repeating units.

  • angstrom

    A common non-SI unit of length, denoted Å, that is used to measure atomic dimensions: 1Å = 10-10 m. (Section 2.3)

  • Aprotic solvent

    A solvent that cannot serve as a hydrogen-bond donor; nowhere in the molecule is there a hydrogen bonded to an atom of high electronegativity. Common aprotic solvents are dichloromethane, diethyl ether, and dimethyl sulfoxide

  • Carbenoid

    A compound that delivers the elements of a carbene without actually producing a free carbene.

  • Delocalization

    The spreading of electron density over a larger volume of space.

  • density

    The ratio of an object’s mass to its volume. (Section 1.4)

  • directed aldol addition

    A techniquefor performing a crossed aldol addition thatproduces one major product.

  • fragmentation

    In mass spectrometry, when the molecular ion breaks apart into fragments.

  • ion–dipole force

    The force that exists between an ion and a neutral polar molecule that possesses a permanent dipole moment. (Section 11.2)

  • isoelectric point (pI)

    For an amino acid, the specific pH at which the concentration of the zwitterionic form reaches its maximum value.

  • isomers

    Compounds whose molecules have the same overall composition but different structures. (Sections 2.9 and 23.4)

  • J value

    When signal splitting occurs in 1H NMR spectroscopy, the distance (in hertz) between the individual peaks of a signal.

  • nitrosonium ion

    The NO+ ion, which is formed when NaNO2 is treated with HCl.

  • Phenol

    A compound that contains an !OH bonded to a benzene ring; a benzenol.

  • reaction quotient (Q)

    The value that is obtained when concentrations of reactants and products are inserted into the equilibrium expression. If the concentrations are equilibrium concentrations, Q = K; otherwise, Q ? K. (Section 15.6)

  • Rearrangement

    A change in connectivity of the atoms in a product compared with the con nectivity of the same atoms in the starting material.

  • saponification

    Hydrolysis of an ester in the presence of a base. (Section 24.4)

  • symmetrical ether

    An ether (R!O!R) where both R groups are identical.

  • Tesla (T)

    The SI unit for magnetic fi eld strength.

  • Zaitsev product

    The more substituted product (alkene) of an elimination reaction.

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