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Solutions for Chapter 7.6: The Addition of Hydrogen Halides and the Addition of Halogens to an Alkyne

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 7.6: The Addition of Hydrogen Halides and the Addition of Halogens to an Alkyne

Solutions for Chapter 7.6
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Since 2 problems in chapter 7.6: The Addition of Hydrogen Halides and the Addition of Halogens to an Alkyne have been answered, more than 7194 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by Patricia and is associated to the ISBN: 9780134042282. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. Chapter 7.6: The Addition of Hydrogen Halides and the Addition of Halogens to an Alkyne includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • acidic cleavage

    A reaction in which bonds are broken in the presence of an acid. For example, in the presence of a strong acid, an ether is converted into two alkyl halides.

  • actinide element

    Element in which the 5f orbitals are only partially occupied. (Section 6.8)

  • Alkylation reaction

    Any reaction in which a new carbon-carbon bond to an alkyl group is formed.

  • auxochrome

    When applying Woodward-Fieser rules, the groups attached to the chromophore.

  • carbon black

    A microcrystalline form of carbon. (Section 22.9)

  • Chain termination

    A step in a chain reaction that involves destruction of reactive intermediates

  • chelate effect

    The generally larger formation constants for polydentate ligands as compared with the corresponding monodentate ligands. (Section 23.3)

  • chelating agent

    A polydentate ligand that is capable of occupying two or more sites in the coordination sphere. (Section 23.3)

  • chemical property.

    Any property of a substance that cannot be studied without converting the substance into some other substance. (1.6)

  • chlorofluorocarbons (CFCs)

    Compound containing only carbon, chlorine, and fluorine.

  • coupling (of protons)

    A phenomenon observed most commonly for nonequivalent protons connected to adjacent carbon atoms in which the multiplicity of each signal is affected by the other.

  • d–d transition

    The transition of an electron in a transition-metal compound from a lower-energy d orbital to a higher-energy d orbital. (Section 23.6)

  • electromagnetic radiation (radiant energy)

    A form of energy that has wave characteristics and that propagates through a vacuum at the characteristic speed of 3.00 * 108 m >s. (Section 6.1)

  • Fishhook arrow

    A barbed curved arrow used to show the change in position of a single electron.

  • lattice energy

    The energy required to separate completely the ions in an ionic solid. (Section 8.2)

  • nucleic acids

    Polymers of high molecular weight that carry genetic information and control protein synthesis. (Section 24.10)

  • nucleophile

    A compound containing an electron-rich atom that is capable of donating a pair of electrons.

  • radical initiator

    A compound with a weak bond that undergoes homolytic bond cleavage with great ease, producing radicals that can initiate a radical chain process.

  • tetravalent

    An element, such as carbon, that forms four bonds.

  • Woodward-Fieser rules

    Rules for predicting the wavelength of maximum absorption for a compound with extended conjugation.

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