×
Log in to StudySoup
Get Full Access to Chemistry - Textbook Survival Guide
Join StudySoup for FREE
Get Full Access to Chemistry - Textbook Survival Guide

Solutions for Chapter 15.8: Esterification

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 15.8: Esterification

Solutions for Chapter 15.8
4 5 0 330 Reviews
14
1

Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. Chapter 15.8: Esterification includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Since 2 problems in chapter 15.8: Esterification have been answered, more than 36553 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions.

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)

  • Alkoxy group

    An !OR group where R is an alkyl group

  • boiling point.

    The temperature at which the vapor pressure of a liquid is equal to the external atmospheric pressure. (11.8)

  • Brønsted-Lowry base

    A compound that can serve as a proton acceptor.

  • carbon black

    A microcrystalline form of carbon. (Section 22.9)

  • chemical shift (d)

    In an NMR spectrum, the location of a signal, defined relative to the frequency of absorption of a reference compound, tetramethylsilane (TMS).

  • crystal-field theory

    A theory that accounts for the colors and the magnetic and other properties of transition-metal complexes in terms of the splitting of the energies of metal ion d orbitals by the electrostatic interaction with the ligands. (Section 23.6)

  • crystalline solid (crystal)

    A solid whose internal arrangement of atoms, molecules, or ions possesses a regularly repeating pattern in any direction through the solid. (Section 12.2)

  • Enantioselective reaction

    A reaction that produces one enantiomer in preference to the other.

  • Enthalpy change, DH

    The difference in total bond strengths and solvation between various points under comparison on a reaction coordinate diagram

  • fuel value

    The energy released when 1 g of a substance is combusted. (Section 5.8)

  • Homolytic bond cleavage

    Cleavage of a bond so that each fragment retains one electron; formation of radicals.

  • hydrocracking

    A process performed in the presence of hydrogen gas by which large alkanes in petroleum are converted into smaller alkanes that are more suitable for use as gasoline.

  • l-Monosaccharide

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

  • Mass spectrum

    A plot of the relative abundance of ions versus their mass-to-charge ratio

  • Oxymercuration-reduction

    A method for converting an alkene to an alcohol. The alkene is treated with mercury(II) acetate followed by reduction with sodium borohydride.

  • Pi (p) bond

    A covalent bond formed by the overlap of parallel 2p orbitals.

  • Sandmeyer reactions

    Reactions that utilize copper salts (CuX) and enable the installation of a halogen or a cyano group on an aromatic ring.

  • Secondary structure of nucleic acids

    The ordered arrangement of nucleic acid strands

  • Trans

    A prefi x meaning across from.

×
Log in to StudySoup
Get Full Access to Chemistry - Textbook Survival Guide
Join StudySoup for FREE
Get Full Access to Chemistry - Textbook Survival Guide
×
Reset your password