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Solutions for Chapter 7.7: The Addition of Water to an Alkyne

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 7.7: The Addition of Water to an Alkyne

Since 3 problems in chapter 7.7: The Addition of Water to an Alkyne have been answered, more than 35403 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 and is associated to the ISBN: 9780321803221. Chapter 7.7: The Addition of Water to an Alkyne includes 3 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7.

Key Chemistry Terms and definitions covered in this textbook
  • aromatic hydrocarbon.

    A hydrocarbon that contains one or more benzene rings. (24.1)

  • bimolecular reaction

    An elementary reaction that involves two molecules. (Section 14.6)

  • carboxylic acids.

    Acids that contain the carboxyl group —COOH. (24.4)

  • cathode.

    The electrode at which reduction occurs. (18.2)

  • Chiral

    From the Greek, cheir meaning hand; an object that is not superposable on its mirror image; an object that has handedness.

  • concentration cell

    A voltaic cell containing the same electrolyte and the same electrode materials in both the anode and cathode compartments. The emf of the cell is derived from a difference in the concentrations of the same electrolyte solutions in the compartments. (Section 20.6)

  • donor atom

    The atom of a ligand that bonds to the metal. (Section 23.2)

  • fracking

    The practice in which water laden with sand and other materials is pumped at high pressure into rock formations to release natural gas and other petroleum materials. (Section 18.4)

  • functional group

    A characteristic group of atoms/bonds that possess a predictable chemical behavior.

  • group

    Elements that are in the same column of the periodic table; elements within the same group or family exhibit similarities in their chemical behavior. (Section 2.5)

  • Haworth projection

    For substituted cycloalkanes, a drawing style used to clearly identify which groups are above the ring and which groups are below the ring. (See also Sect. 4.14.)

  • hydrolysis

    A reaction in which bonds are cleaved by treatment with water.

  • imine

    A compound containing a CRN bond.

  • isoelectric point (pI)

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

  • molar heat capacity

    The heat required to raise the temperature of one mole of a substance by 1 °C. (Section 5.5)

  • retention time

    The amount of time required for a compound to exit from a gas chromatograph.

  • saponification

    The base-catalyzed hydrolysis of an ester. This method is used to make soap.

  • Unimolecular reaction

    A reaction in which only one species is involved in the rate-determining step

  • Valence Bond Theory

    A model of bonding that places electron pairs between adjacent atoms to create bonds.

  • Wittig reaction

    A reaction that converts an aldehyde or ketone into an alkene, with the introduction of one or more carbon atoms.

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