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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 25577 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 and is associated to the ISBN: 9780073402741.

Key Chemistry Terms and definitions covered in this textbook
  • amphoteric oxides and hydroxides

    Oxides and hydroxides that are only slightly soluble in water but that dissolve in either acidic or basic solutions. (Section 17.5)

  • Carbocation

    A species in which a carbon atom has only six electrons in its valence shell and bears a positive charge

  • chemical kinetics.

    The area of chemistry concerned with the speeds, or rates, at which chemical reactions occur. (13.1)

  • chiral.

    Compounds or ions that are not superimposable with their mirror images. (23.4)

  • coordination number

    The number of adjacent atoms to which an atom is directly bonded. In a complex the coordination number of the metal ion is the number of donor atoms to which it is bonded. (Sections 12.37 and 24.2)

  • Curved arrow

    A symbol used to show the redistribution of valence electrons in resonance contributing structures or reactions, symbolizing movement of two electrons

  • diastereomers

    Stereoisomers that are not mirror images of one another.

  • electrostatic potential maps

    A three-dimensional, rainbowlike image used to visualize partial charges in a compound.

  • epimer

    Diastereomers that differ from each other in the configuration of only one chirality center.

  • fuel cell

    A voltaic cell that utilizes the oxidation of a conventional fuel, such as H2 or CH4, in the cell reaction. (Section 20.7)

  • gauche interaction

    The steric interaction that results when two groups in a Newman projection are separated by a dihedral angle of 60°.

  • hydrogen bonding

    A special type of dipole-dipole interaction that occurs between an electronegative atom and a hydrogen atom that is connected to another electronegative atom.

  • isotactic

    A polymer in which the repeating units contain chirality centers which all have the same configuration.

  • lone pair

    A pair of unshared, or nonbonding, electrons.

  • Molecular ion (M1)

    The radical cation formed by removal of a single electron from a parent molecule in a mass spectrometer.

  • nonpolar covalent bond

    A covalent bond in which the electrons are shared equally. (Section 8.4) normal boiling point The boiling point at 1 atm pressure. (Section 11.5)

  • optical isomerism

    A form of isomerism in which the two forms of a compound (stereoisomers) are nonsuperimposable mirror images. (Section 23.4)

  • Organometallic compound

    A compound that contains a carbon-metal bond.

  • ozonolysis

    A reaction in which the CRC bond of an alkene is cleaved to form two CRO bonds.

  • second order

    A reaction that has a rate equation in which the sum of all exponents is two.

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