Solutions for Chapter 6: Addition Reactions of 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: Addition Reactions of Alkenes

Solutions for Chapter 6
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Textbook: Organic Chemistry,
Edition: 9
Author: Francis A Carey Dr., Robert M. Giuliano
ISBN: 9780073402741

Chapter 6: Addition Reactions of Alkenes includes 44 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Since 44 problems in chapter 6: Addition Reactions of Alkenes have been answered, more than 10876 students have viewed full step-by-step solutions from this chapter. 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.

Key Chemistry Terms and definitions covered in this textbook
  • alkali metals.

    The Group 1A elements (Li, Na, K, Rb, Cs, and Fr). (2.4)

  • Benzyl group (C6H5CH2!)

    The group derived from toluene by removing a hydrogen from its methyl group.

  • Betaine

    A neutral molecule with nonadjacent positive and negative charges. An example of a betaine is the intermediate formed by addition of a Wittig reagent to an aldehyde or ketone

  • decomposition reaction.

    The breakdown of a compound into two or more components. (4.4)

  • diamagnetism

    A type of magnetism that causes a substance with no unpaired electrons to be weakly repelled from a magnetic field. (Section 9.8)

  • diastereomers

    Stereoisomers that are not mirror images of one another.

  • flagpole interactions

    For cyclohexane, the steric interactions that occur between the flagpole hydrogen atoms in a boat conformation.

  • Hell-Volhard-Zelinsky reaction

    A reaction in which a carboxylic acid undergoes a-halogenation when treated with bromine in the presence of PBr3.

  • hemiacetal

    A compound containing a hydroxyl group (OH) and an alkoxy group (OR) connected to the same carbon atom.

  • hybrid orbital

    An orbital that results from the mixing of different kinds of atomic orbitals on the same atom. For example, an sp3 hybrid results from the mixing, or hybridizing, of one s orbital and three p orbitals. (Section 9.5)

  • hydration

    A reaction in which a proton and a hydroxyl group (OH) are added across a p bond.

  • Lactam

    A cyclic amide.

  • mass spectrometer

    An instrument used to measure the precise masses and relative amounts of atomic and molecular ions. (Section 2.4)

  • metallic bond

    Bonding, usually in solid metals, in which the bonding electrons are relatively free to move throughout the three-dimensional structure. (Section 8.1)

  • mole fraction

    The ratio of the number of moles of one component of a mixture to the total moles of all components; abbreviated X, with a subscript to identify the component. (Section 10.6)

  • N-glycoside

    The product obtained when a monosaccharide is treated with an amine in the presence of an acid catalyst.

  • nitration

    An electrophilic aromatic substitution reaction that involves the installation of a nitro group (NO2) on an aromatic ring.

  • optically active

    A compound that rotates plane-polarized light.

  • quintet

    In NMR spectroscopy, a signal that is comprised of five peaks.

  • solubility

    The amount of a substance that dissolves in a given quantity of solvent at a given temperature to form a saturated solution. (Sections 4.2 and 13.2)

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