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Solutions for Chapter 20.7: The Haloform Reaction

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 20.7: The Haloform Reaction

Solutions for Chapter 20.7
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Since 1 problems in chapter 20.7: The Haloform Reaction have been answered, more than 7383 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 20.7: The Haloform Reaction includes 1 full step-by-step solutions. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741.

Key Chemistry Terms and definitions covered in this textbook
  • acetoacetic ester synthesis

    A threestep process that converts an alkyl halide into a methyl ketone with the introduction of three new carbon atoms.

  • acylium ion

    The resonancestabilized, cationic intermediate of a Friedel-Crafts acylation, formed by treating an acyl halide with aluminum trichloride.

  • amorphous solid.

    A solid that lacks a regular three-dimensional arrangement of atoms or molecules. (11.7)

  • binary compounds.

    Compounds formed from just two elements. (2.7)

  • Brønsted–Lowry acid

    A substance (molecule or ion) that acts as a proton donor. (Section 16.2)

  • chlorofluorocarbons

    Compounds composed entirely of chlorine, fluorine, and carbon. (Section 18.3)

  • electron density

    A term associatedwith the probability of finding an electron in aparticular region of space.

  • Electrophoresis

    The process of separating compounds on the basis of their electric charge

  • ferrimagnetism

    A form of magnetism in which unpaired electron spins on different-type ions point in opposite directions but do not fully cancel out. (Section 23.1)

  • fuel value

    The energy released when 1 g of a substance is combusted. (Section 5.8)

  • fusion

    The joining of two light nuclei to form a more massive one. (Section 21.6)

  • heat of fusion

    The enthalpy change, ?H, for melting a solid. (Section 11.4)

  • hydrocracking

    A process performed in the presence of hydrogen gas by which large alkanes in petroleum are converted into smaller alkanes that are more suitable for use as gasoline.

  • Lipid

    A biomolecule isolated from plant or animal sources by extraction with nonpolar organic solvents, such as diethyl ether and hexane.

  • molecular orbital (MO)

    An allowed state for an electron in a molecule. According to molecular-orbital theory, a molecular orbital is entirely analogous to an atomic orbital, which is an allowed state for an electron in an atom. Most bonding molecular orbitals can be classified as s or p, depending on the disposition of electron density with respect to the internuclear axis. (Section 9.7)

  • photodissociation

    The breaking of a molecule into two or more neutral fragments as a result of absorption of light. (Section 18.2)

  • reaction mechanism

    A series of intermediates and curved arrows that show howthe reaction occurs in terms of the motion of electrons.

  • reductive amination

    The conversion of a ketone or aldehyde into an imine under conditions in which the imine is reduced as soon as it is formed, giving an amine.

  • secondary cell

    A voltaic cell that can be recharged. (Section 20.7)

  • spectroscopy

    The study of the interaction between matter and electromagnetic radiation.

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