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Solutions for Chapter 16.9: The Reactions of Esters

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 16.9: The Reactions of Esters

Organic Chemistry was written by and is associated to the ISBN: 9780321803221. Since 4 problems in chapter 16.9: The Reactions of Esters have been answered, more than 41465 students have viewed full step-by-step solutions from this chapter. Chapter 16.9: The Reactions of Esters includes 4 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • absorbance

    In UV-Vis spectroscopy, the value log (I0/I) where I0 is the intensity of the reference beam and I is the intensity of the sample beam.

  • alcohol

    An organic compound obtained by substituting a hydroxyl group 1┬ČOH2 for a hydrogen on a hydrocarbon. (Sections 2.9 and 24.4)

  • aldonic acid

    The product obtained when the aldehyde group of an aldose is oxidized.

  • antibonding molecular orbital.

    A molecular orbital that is of higher energy and lower stability than the atomic orbitals from which it was formed. (10.6)

  • atomic mass.

    The mass of an atom in atomic mass units. (3.1)

  • Birch reduction

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

  • body-centered lattice

    A crystal lattice in which the lattice points are located at the center and corners of each unit cell. (Section 12.2)

  • catalyst

    A substance that changes the speed of a chemical reaction without itself undergoing a permanent chemical change in the process. (Section 14.7)

  • enantiomeric excess

    For a mixture containing two enantiomers, the difference between the percent concentration of the major enantiomer and the percent concentration of its mirror image.

  • exchange (metathesis) reaction

    A reaction between compounds that when written as a molecular equation appears to involve the exchange of ions between the two reactants. (Section 4.2)

  • glass transition temperature (Tg)

    The temperature at which noncrystalline polymers become very soft.

  • green chemistry

    Chemistry that promotes the design and application of chemical products and processes that are compatible with human health and that preserve the environment. (Section 18.5)

  • heat of sublimation

    The enthalpy change, ?H, for vaporization of a solid. (Section 11.4)

  • Hydroxyl group

    An !OH group

  • Michael reaction

    A reaction in which a nucleophile attacks a conjugated p system, resulting in a 1,4-addition.

  • Molar absorptivity (e)

    The absorbance of a 1 M solution of a compound.

  • percent ionization

    The percent of a substance that undergoes ionization on dissolution in water. The term applies to solutions of weak acids and bases. (Section 16.6)

  • Secondary structure of nucleic acids

    The ordered arrangement of nucleic acid strands

  • step-growth polymers

    Polymers that are formed under conditions in which the individual monomers react with each other to form oligomers, which are then joined together to form polymers.

  • twist boat

    A conformation of cyclohexane that is lower in energy than a boat conformation but higher in energy than a chair conformation.

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