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Solutions for Chapter 17: Carboxylic Acids

Organic Chemistry | 7th Edition | ISBN: 9781133952848 | Authors: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9781133952848

Organic Chemistry | 7th Edition | ISBN: 9781133952848 | Authors: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Solutions for Chapter 17: Carboxylic Acids

Solutions for Chapter 17
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Textbook: Organic Chemistry
Edition: 7
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
ISBN: 9781133952848

This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Since 48 problems in chapter 17: Carboxylic Acids have been answered, more than 7523 students have viewed full step-by-step solutions from this chapter. Chapter 17: Carboxylic Acids includes 48 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by and is associated to the ISBN: 9781133952848.

Key Chemistry Terms and definitions covered in this textbook
  • alkene

    A compound that possesses a carbon-carbon double bond.

  • alkylation

    A reaction that achieves the installation of an alkyl group. For example, an SN2 reaction in which an alkyl group is connected to an attacking nucleophile.

  • alkynes.

    Hydrocarbons that contain one or more carbon-carbon triple bonds. They have the general formula CnH2n22, where n 5 2,3, . . . . (24.2)

  • Base peak

    The peak caused by the most abundant ion in a mass spectrum; the most intense peak. It is assigned an arbitrary intensity of 100

  • blocking group

    A group that can be readily installed and uninstalled. Used for regiochemical control during synthesis.

  • carbohydrates

    A class of substances formed from polyhydroxy aldehydes or ketones. (Section 24.8)

  • chemical equilibrium

    A state of dynamic balance in which the rate of formation of the products of a reaction from the reactants equals the rate of formation of the reactants from the products; at equilibrium the concentrations of the reactants and products remain constant. (Section 4.1;Chapter 15: Introduction)

  • configuration

    The 3D spatial orientation of the groups connected to a chirality center (R or S ) or of the groups in a stereoisiomeric alkene (E or Z).

  • core electrons.

    All nonvalence electrons in an atom. (8.2)

  • electrolytic cell

    A device in which a nonspontaneous oxidation–reduction reaction is caused to occur by passage of current under a sufficient external electrical potential. (Section 20.9)

  • Enamine

    An unsaturated compound derived by the reaction of an aldehyde or ketone and a secondary amine followed by loss of H2O; R2C"CR!NR2

  • l-Monosaccharide

    A monosaccharide that, when written as a Fischer projection, has the !OH on its penultimate carbon to the left.

  • meso compound

    A compound that possesses chirality centers and an internal plane of symmetry.

  • Nernst equation

    An equation that relates the cell emf, E, to the standard emf, E°, and the reaction quotient, Q: E = E° - 1RT>nF2 ln Q. (Section 20.6)

  • nonaromatic

    A compound that lacks a ring with a continuous system of overlapping p orbitals.

  • oxyacid

    A compound in which one or more OH groups, and possibly additional oxygen atoms, are bonded to a central atom. (Section 16.10)

  • Pericyclic reaction

    A reaction that takes place in a single step, without intermediates, and involves a cyclic redistribution of bonding electrons

  • Potential energy

    The energy that can be released if given an opportunity

  • proton

    A positively charged subatomic particle found in the nucleus of an atom. (Section 2.3)

  • Telechelic polymer

    A polymer in which its growing chains are terminated by formation of new functional groups at both ends of its chains. These new functional groups are introduced by adding reagents, such as CO2 or ethylene oxide, to the growing chains.

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