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Solutions for Chapter 7: Alkyl Halides and Nucleophilic Substitution

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 7: Alkyl Halides and Nucleophilic Substitution

Solutions for Chapter 7
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Textbook: Organic Chemistry
Edition: 3
Author: Janice Gorzynski Smith
ISBN: 9780077354725

This expansive textbook survival guide covers the following chapters and their solutions. Chapter 7: Alkyl Halides and Nucleophilic Substitution includes 80 full step-by-step solutions. Since 80 problems in chapter 7: Alkyl Halides and Nucleophilic Substitution have been answered, more than 66263 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 3. Organic Chemistry was written by and is associated to the ISBN: 9780077354725.

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

    Polymerization that occurs through coupling of monomers with one another, with no other products formed in the reaction. (Section 12.8)

  • bonding atomic radius

    The radius of an atom as defined by the distances separating it from other atoms to which it is chemically bonded. (Section 7.3)

  • Boyle’s law.

    The volume of a fixed amount of gas maintained at constant temperature is inversely proportional to the gas pressure. (5.3)

  • Chiral center

    A tetrahedral atom, most commonly carbon, that is bonded to four different groups; also called a chirality center

  • conductor.

    Substance capable of conducting electric current. (21.3)

  • conservation of orbital symmetry

    During a reaction, the requirement that the phases of the frontier MOs must be aligned.

  • copolymer.

    A polymer containing two or more different monomers. (25.2)

  • cycloaddition reactions

    Reactions in which two p systems are joined together in a way that forms a ring. In the process, two p bonds are converted into two s bonds.

  • dipole

    A molecule with one end having a partial negative charge and the other end having a partial positive charge; a polar molecule. (Section 8.4)

  • exergonic

    Any process with a negative DG.

  • half-life

    The time required for the concentration of a reactant substance to decrease to half its initial value; the time required for half of a sample of a particular radioisotope to decay. (Sections 14.4 and 21.4)

  • ignal splitting in NMR

    Spin-spin coupling with adjacent nuclei split NMR signals depending on the extent of coupling and the number of adjacent equivalent nuclei.

  • molecular hydrides

    Compounds formed when hydrogen reacts with nonmetals and metalloids. (Section 22.2)

  • nucleotide

    Compounds formed from a molecule of phosphoric acid, a sugar molecule, and an organic nitrogen base. Nucleotides form linear polymers called DNA and RNA, which are involved in protein synthesis and cell reproduction. (Section 24.10)

  • Phenyl group

    A group derived by removing an H from benzene; abbreviated C6H5! or Ph!.

  • quartet

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

  • radiotracer

    A radioisotope that can be used to trace the path of an element in a chemical system. (Section 21.5)

  • sp3-hybridized orbitals

    Atomic orbitals that are achieved by mathematically averaging one s orbital with three p orbitals to form four hybridized atomic orbitals.

  • substitution reactions

    Reactions in which one group is replaced by another group.

  • wavenumber

    In IR spectroscopy, the location of each signal is reported in terms of this frequency-related unit.

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