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Solutions for Chapter 11.5: Oxidation of Alcohols

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 11.5: Oxidation of Alcohols

Solutions for Chapter 11.5
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This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Organic Chemistry was written by and is associated to the ISBN: 9780321803221. Since 1 problems in chapter 11.5: Oxidation of Alcohols have been answered, more than 35712 students have viewed full step-by-step solutions from this chapter. Chapter 11.5: Oxidation of Alcohols includes 1 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • aldehyde

    An organic compound that contains a carbonyl group 1C “O2 to which at least one hydrogen atom is attached. (Section 24.4)

  • anion.

    An ion with a net negative charge. (2.5)

  • base

    A substance that is an H+ acceptor; a base produces an excess of OH-1aq2 ions when it dissolves in water. (Section 4.3)

  • Birch reduction

    A reaction in which benzene is reduced to give 1,4-cyclohexadiene.

  • Brønsted acid.

    A substance capable of donating a proton. (4.3)

  • carbonyl group

    The C “O double bond, a characteristic feature of several organic functional groups, such as ketones and aldehydes. (Section 24.4)

  • Center of symmetry

    A point so situated that identical components of an object are located on opposite sides and equidistant from that point along any axis passing through it.

  • chlor-alkali process.

    The production of chlorine gas by the electrolysis of aqueous NaCl solution. (22.6)

  • Claisen rearrangement

    A [3,3] sigmatropic rearrangement that is observed for allylic vinylic ethers.

  • Condensation polymerization

    A polymerization in which chain growth occurs in a stepwise manner between difunctional monomers. Also called step-growth polymerization.

  • Friedel-Crafts acylation

    An electrophilic aromatic substitution reaction that installs an acyl group on an aromatic ring.

  • Lactone

    A cyclic ester.

  • oxyanion

    A polyatomic anion that contains one or more oxygen atoms. (Section 2.8)

  • oxymercuration-demercuration

    A two-step process for the Markovnikov addition of water across an alkene. With this process, carbocation rearrangements do not occur.

  • phenolate

    The conjugate base of phenol or a substituted phenol.

  • polyatomic ion

    An electrically charged group of two or more atoms. (Section 2.7)

  • salt

    An ionic compound formed by replacing one or more hydrogens of an acid by other cations. (Section 4.3)

  • secondary alkyl halide

    An organohalide in which the alpha (a) position is connected to exactly two alkyl groups.

  • Stork enamine synthesis

    A Michaelreaction in which an enamine functions as anucleophile.

  • vinylic carbocation

    A carbocation in which the positive charge resides on a vinylic carbon atom. This type of carbocation is very unstable and will not readily form in most cases.

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