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Solutions for Chapter 5.2: REACTIONS OF ALkENES WITH HALOgENS

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Full solutions for Organic Chemistry | 6th Edition

ISBN: 9781936221349

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Solutions for Chapter 5.2: REACTIONS OF ALkENES WITH HALOgENS

Solutions for Chapter 5.2
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This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 5.2: REACTIONS OF ALkENES WITH HALOgENS have been answered, more than 39564 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. Organic Chemistry was written by and is associated to the ISBN: 9781936221349. Chapter 5.2: REACTIONS OF ALkENES WITH HALOgENS includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • (n 1 1) rule

    If a hydrogen has n hydrogens nonequivalent to it but equivalent among themselves on the same or adjacent atom(s), its 1 H!NMR signal is split into (n 1 1) peaks

  • bending

    In IR spectroscopy, a type of vibration that generally produces a signal in the fingerprint region of an IR spectrum.

  • bond-line structures

    The most common drawing style employed by organic chemists. All carbon atoms and most hydrogen atoms are implied but not explicitly drawn in a bond-line structure.

  • branched polymer

    A polymer that contains a large number of branches connected to the main chain of the polymer.

  • Carbanion

    An ion in which carbon has an unshared pair of electrons and bears a negative charge.

  • carboxylic acids.

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

  • crystallization.

    The process in which dissolved solute comes out of solution and forms crystals. (12.1)

  • doublet

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

  • Enantioselective reaction

    A reaction that produces one enantiomer in preference to the other.

  • Fluid-mosaic model

    A biological membrane that consists of a phospholipid bilayer with proteins, carbohydrates, and other lipids on the surface and embedded in the bilayer

  • Hybrid orbital

    An orbital formed by the combination of two or more atomic orbitals.

  • Lewis dot structure

    The symbol of an element surrounded by a number of dots equal to the number of electrons in the valence shell of the atom

  • nanomaterial

    A solid whose dimensions range from 1 to 100 nm and whose properties differ from those of a bulk material with the same composition. (Section 12.1)

  • Nitrile

    A compound containing a !C#N (cyano) group bonded to a carbon atom.

  • oxime

    A compound with the structure R2CRN!OH.

  • Polar covalent bond

    A covalent bond between atoms whose difference in electronegativity is between approximately 0.5 and 1.9.

  • R (Section 3.3)

    From the Latin, rectus, straight, correct; used in the R,S convention to show that the order of priority of groups on a chiral center is clockwise.

  • retention time

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

  • Thermochemistry

    The study of the energy of chemical structures.

  • vinylic carbocation

    A carbocation in which the positive charge resides on a vinylic carbon atom. This type of carbocation is very unstable and will not readily form in most cases.