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Solutions for Chapter 10: Elimination Reactions of Alkyl Halides Competition Between Substitution and Elimination

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 10: Elimination Reactions of Alkyl Halides Competition Between Substitution and Elimination

Solutions for Chapter 10
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Textbook: Organic Chemistry
Edition: 7
Author: Paula Yurkanis Bruice
ISBN: 9780321803221

Since 35 problems in chapter 10: Elimination Reactions of Alkyl Halides Competition Between Substitution and Elimination have been answered, more than 8644 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by Patricia and is associated to the ISBN: 9780321803221. Chapter 10: Elimination Reactions of Alkyl Halides Competition Between Substitution and Elimination includes 35 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7.

Key Chemistry Terms and definitions covered in this textbook
  • asymmetric hydrogenation

    The addition of H2 across only one face of a p bond.

  • base.

    A substance that yields hydroxide ions (OH2) when dissolved in water. (2.7)

  • Carbonyl group (Section 1.3C)

    A C"O group.

  • Chemical shift (d)

    The shift in parts per million of an NMR signal relative to the signal of TMS

  • density

    The ratio of an object’s mass to its volume. (Section 1.4)

  • desalination

    The removal of salts from seawater, brine, or brackish water to make it fit for human consumption. (Section 18.4)

  • Heterocyclic aromatic amine

    An amine in which nitrogen is one of the atoms of an aromatic ring.

  • Hofmann rule

    Any b-elimination that occurs preferentially to give the less substituted alkene as the major product.

  • immiscible liquids

    Liquids that do not dissolve in one another to a significant extent. (Section 13.3)

  • Lactone

    A cyclic ester.

  • lipid bilayer

    The main fabricof cell membranes, assembled primarily fromphosphoglycerides.

  • nucleophilic attack

    One of the four arrow-pushing patterns for ionic reactions.

  • Orthogonal

    Having no net overlap.

  • phospholipid

    A form of lipid molecule that contains charged phosphate groups. (Section 24.9)

  • Pyranose

    A six-membered cyclic form of a monosaccharide.

  • quantitative analysis

    The determination of the amount of a given substance that is present in a sample. (Section 17.7)

  • quaternary structure

    The structure that arises when a protein consists of two or more folded polypeptide chains that aggregate to form one protein complex.

  • Sanger dideoxy method

    A method developed by Frederick Sanger for sequencing DNA molecules

  • strong deactivators

    Groups that strongy deactivate an aromatic ring toward electrophilic aromatic substitution, thereby significantly decreasing the rate of the reaction.

  • Substitution

    A reaction in which an atom or group of atoms in a compound is replaced by another atom or group of atoms.

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