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Solutions for Chapter 9.7: summary of substitution and elimination reactions of alkyl Halides

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 9.7: summary of substitution and elimination reactions of alkyl Halides

Solutions for Chapter 9.7
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Since 1 problems in chapter 9.7: summary of substitution and elimination reactions of alkyl Halides have been answered, more than 36591 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. 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 9.7: summary of substitution and elimination reactions of alkyl Halides includes 1 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • addition reaction

    A reaction in which a reagent adds to the two carbon atoms of a carbon–carbon multiple bond. (Section 24.3)

  • antioxidants

    Radical scavengers that prevent autooxidation by preventing radical chain reactions from beginning.

  • chemical properties

    Properties that describe a substance’s composition and its reactivity; how the substance reacts or changes into other substances. (Section 1.3)

  • conductor.

    Substance capable of conducting electric current. (21.3)

  • coordination compound

    A compound containing a metal ion bonded to a group of surrounding molecules or ions that act as ligands. (Section 23.2)

  • Coupling constant

    The separation on an NMR spectrum (in hertz) between adjacent peaks in a multiplet and a quantitative measure of the infl uence of the spin-spin coupling with adjacent nuclei.

  • diffusion.

    The gradual mixing of molecules of one gas with the molecules of another by virtue of their kinetic properties. (5.7)

  • E2

    A bimolecular eliminationreaction.eclipsed conformation (Sect. 4.7): A conformationin which groups are eclipsing each other in aNewman projection.

  • enthalpy of formation

    The enthalpy change that accompanies the formation of a substance from the most stable forms of its component elements. (Section 5.7)

  • fingerprint region

    The region of an IR spectrum that contains signals resulting from the vibrational excitation of most single bonds (stretching and bending).

  • Infrared (IR) spectroscopy

    A spectroscopic technique in which a compound is irradiated with infrared radiation, absorption of which causes covalent bonds to change from a lower vibration state to a higher one. Infrared spectroscopy is particularly valuable for determining the kinds of functional groups present in a molecule.

  • intensive property

    A property that is independent of the amount of material considered, for example, density. (Section 1.3)

  • Markovnikov addition

    In additionreactions, the observation that the hydrogen atomis generally placed at the vinylic position alreadybearing the larger number of hydrogen atoms.

  • nuclear binding energy

    The energy required to decompose an atomic nucleus into its component protons and neutrons. (Section 21.6)

  • photoelectric effect

    The emission of electrons from a metal surface induced by light. (Section 6.2)

  • radical

    A chemical entity with an unpaired electron.

  • Solvolysis

    A nucleophilic substitution in which the solvent is also the nucleophile

  • Terpene

    A compound whose carbon skeleton can be divided into two or more units identical with the carbon skeleton of isoprene

  • Valence-shell electron-pair repulsion (VSEPR)

    A method for predicting bond angles based on the idea that electron pairs repel each other and keep as far apart as possible.

  • Vicinal coupling

    a !CH"CH2 group

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