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Solutions for Chapter 11: Organic Chemistry 8th Edition

Organic Chemistry | 8th Edition | ISBN: 9780321768414 | Authors: L.G. Wade Jr

Full solutions for Organic Chemistry | 8th Edition

ISBN: 9780321768414

Organic Chemistry | 8th Edition | ISBN: 9780321768414 | Authors: L.G. Wade Jr

Solutions for Chapter 11

Solutions for Chapter 11
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Textbook: Organic Chemistry
Edition: 8
Author: L.G. Wade Jr
ISBN: 9780321768414

Chapter 11 includes 56 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Since 56 problems in chapter 11 have been answered, more than 152306 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by and is associated to the ISBN: 9780321768414. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8.

Key Chemistry Terms and definitions covered in this textbook
  • Alkoxy group

    An !OR group where R is an alkyl group

  • alkyl group

    A group that is formed by removing a hydrogen atom from an alkane. (Section 25.3)

  • aromatic

    A compound containing a planar ring of continuously overlapping p orbitals with 4n+2p electrons.

  • boat conformation

    A conformation of cyclohexane in which all bond angles are fairly close to 109.5° and many hydrogen atoms are eclipsing each other.

  • boranes

    Covalent hydrides of boron. (Section 22.11)

  • chlorohydrin

    A compound containing a Cl group and a hydroxyl group (OH) on adjacent carbon atoms.

  • cholesteric liquid crystalline phase

    A liquid crystal formed from flat, disc-shaped molecules that align through a stacking of the molecular discs. (Section 11.7)

  • combustion reaction.

    A reaction in which a substance reacts with oxygen, usually with the release of heat and light, to produce a flame. (4.4)

  • constructive interference

    When two waves interact with each other in a way that produces a wave with a larger amplitude.

  • Dehydration

    Elimination of water.

  • d–d transition

    The transition of an electron in a transition-metal compound from a lower-energy d orbital to a higher-energy d orbital. (Section 23.6)

  • Edman degradation

    A method for analyzing the sequence of amino acids in apeptide by removing one amino acid residue at a time and identifying each residue as it is removed.

  • fats

    Triglycerides that are solids atroom temperature.

  • Hammond postulate

    In an exothermic process the transition state is closer in energy to the reactants than to the products, and therefore the structure of the transition state more closely resembles the reactants. In contrast, the transition state in an endothermic process is closer in energy to the products, and therefore the transition state more closely resembles the products.

  • hydrohalogenation

    A reaction that involves the addition of H and X (either Br or Cl) across an alkene.

  • isolated diene

    A compound containing two carbon-carbon p bonds that are separated by two or more s bonds.

  • Lewis structures

    A drawing style inwhich the electrons take center stage.linear polymer (Sect. 27.6): A polymer thathas only a minimal amount of branching or nobranching at all.

  • Lewis symbol (electron-dot symbol)

    The chemical symbol for an element, with a dot for each valence electron. (Section 8.1)

  • loss of a leaving group

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

  • Nucleophilic substitution

    Any reaction in which one nucleophile is substituted for another at a tetravalent carbon atom.

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