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Solutions for Chapter 8: Alkyl Halides and Elimination Reactions

Organic Chemistry | 3rd Edition | ISBN: 9780077354725 | Authors: Janice Gorzynski Smith

Full solutions for Organic Chemistry | 3rd Edition

ISBN: 9780077354725

Organic Chemistry | 3rd Edition | ISBN: 9780077354725 | Authors: Janice Gorzynski Smith

Solutions for Chapter 8: Alkyl Halides and Elimination Reactions

Solutions for Chapter 8
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Textbook: Organic Chemistry
Edition: 3
Author: Janice Gorzynski Smith
ISBN: 9780077354725

Chapter 8: Alkyl Halides and Elimination Reactions includes 62 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9780077354725. Since 62 problems in chapter 8: Alkyl Halides and Elimination Reactions have been answered, more than 34857 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 3. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • addition to p bond

    One of the six kinds of arrow-pushing patterns used in drawing mechanisms for radical reactions. A radical adds to a p bond, destroying the p bond and generating a new radical.

  • beta (b) position

    The position immediately adjacent to an alpha (a) position.

  • Bredt’s rule

    A rule that states that it is not possible for a bridgehead carbon of a bicyclic system to possess a carbon carbon double bond if it involves a trans p bond being incorporated in a ring comprised of fewer than eight atoms.

  • chemical equilibrium

    A state of dynamic balance in which the rate of formation of the products of a reaction from the reactants equals the rate of formation of the reactants from the products; at equilibrium the concentrations of the reactants and products remain constant. (Section 4.1;Chapter 15: Introduction)

  • Conjugate addition

    Addition of a nucleophile to the b-carbon of an a,b-unsaturated carbonyl compound. (Section 20.2A) Addition to carbons 1 and 4 of a conjugated diene.

  • Conjugated

    A conjugated diene or carbonyl is one in which the double bonds are separated by one single bond

  • excited state

    A state that is achieved when a compound absorbs energy.

  • first-order reaction

    A reaction in which the reaction rate is proportional to the concentration of a single reactant, raised to the first power. (Section 14.4)

  • Haworth projection

    A way to view furanose and pyranose forms of monosaccharides. The ring is drawn fl at and most commonly viewed through its edge with the anomeric carbon on the right and the oxygen atom of the ring to the rear

  • homopolymer

    A polymer constructed from a single type of monomer.

  • lipid bilayer

    The main fabricof cell membranes, assembled primarily fromphosphoglycerides.

  • Messenger RNA (mRNA)

    A ribonucleic acid that carries coded genetic information from DNA to the ribosomes for the synthesis of proteins

  • natural gas

    A naturally occurring mixture of gaseous hydrocarbon compounds composed of hydrogen and carbon. (Section 5.8)

  • overlap

    The extent to which atomic orbitals on different atoms share the same region of space. When the overlap between two orbitals is large, a strong bond may be formed. (Section 9.4)

  • particle accelerator

    A device that uses strong magnetic and electrostatic fields to accelerate charged particles. (Section 21.3)

  • photosynthesis

    The process that occurs in plant leaves by which light energy is used to convert carbon dioxide and water to carbohydrates and oxygen. (Section 23.3)

  • Radical inhibitor

    A compound such as a phenol that selectively reacts with radicals to remove them from a chain reaction and terminate the chain

  • SN2

    A bimolecular nucleophilic substitution reaction.

  • spin magnetic quantum number 1ms2

    A quantum number associated with the electron spin; it may have values of +12 or -12. (Section 6.7)

  • Staggered conformation

    A conformation about a carbon-carbon single bond in which the atoms or groups on one carbon are as far apart as possible from atoms or groups on an adjacent carbon.

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