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Solutions for Chapter 6.9: The Addition of a Halogen to an Alkene

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 6.9: The Addition of a Halogen to an Alkene

Organic Chemistry was written by Patricia and is associated to the ISBN: 9780321803221. Chapter 6.9: The Addition of a Halogen to an Alkene includes 7 full step-by-step solutions. Since 7 problems in chapter 6.9: The Addition of a Halogen to an Alkene have been answered, more than 8386 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • acetylide ion

    The conjugate base of acetylene or any terminal alkyne.

  • alditol

    The product obtained when the aldehyde group of an aldose is reduced.

  • Bonding electrons

    Valence electrons involved in forming a covalent bond (i.e., shared electrons).

  • calcination

    The heating of an ore to bring about its decomposition and the elimination of a volatile product. For example, a carbonate ore might be calcined to drive off CO2. (Section 23.2)

  • chlorofluorocarbons (CFCs)

    Compound containing only carbon, chlorine, and fluorine.

  • dihydroxylation

    A reaction characterized by the addition of two hydroxyl groups (OH) across an alkene.

  • ether

    A compound with the structure R!O!R.

  • heat of reaction

    The heat given off during a reaction.

  • hydrophilic

    A polar group that has favorable interactions with water.

  • ionization energy

    The energy required to remove an electron from a gaseous atom when the atom is in its ground state. (Section 7.4)

  • ion–dipole force

    The force that exists between an ion and a neutral polar molecule that possesses a permanent dipole moment. (Section 11.2)

  • isoelectronic series

    A series of atoms, ions, or molecules having the same number of electrons. (Section 7.3)

  • l amino acid

    Amino acids with Fischer projections that resemble the Fischer projections of l sugars.

  • l sugar

    A carbohydrate for which the chirality center farthest from the carbonyl group will have an OH group pointing to the left in the Fischer projection.

  • Node

    A point in space where the value of a wave function is zero

  • percent ionization

    The percent of a substance that undergoes ionization on dissolution in water. The term applies to solutions of weak acids and bases. (Section 16.6)

  • Polycarbonate

    A polyester in which the carboxyl groups are derived from carbonic acid

  • ring flip

    A conformational change in which one chair conformation is converted into the other.

  • spontaneous process

    A process that is capable of proceeding in a given direction, as written or described, without needing to be driven by an outside source of energy. A process may be spontaneous even though it is very slow. (Section 19.1)

  • tetrahedral intermediate

    An intermediate with tetrahedral geometry. This type of intermediate is formed when a nucleophile attacks the carbonyl group of a carboxylic acid derivative.

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