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Solutions for Chapter 25.5: REACTIONS OF THIOESTERS WITH NUClEOpHIlES Thioesters, like

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Full solutions for Organic Chemistry | 6th Edition

ISBN: 9781936221349

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Solutions for Chapter 25.5: REACTIONS OF THIOESTERS WITH NUClEOpHIlES Thioesters, like

Solutions for Chapter 25.5
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Organic Chemistry was written by and is associated to the ISBN: 9781936221349. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. Chapter 25.5: REACTIONS OF THIOESTERS WITH NUClEOpHIlES Thioesters, like includes 2 full step-by-step solutions. Since 2 problems in chapter 25.5: REACTIONS OF THIOESTERS WITH NUClEOpHIlES Thioesters, like have been answered, more than 39972 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • activate

    For a substituted aromatic ring, the effect of an electron-donating substituent that increases the rate of electrophilic aromatic substitution.

  • alkanes

    Compounds of carbon and hydrogen containing only carbon–carbon single bonds. (Sections 2.9 and 24.2)

  • Alkoxy group

    An !OR group where R is an alkyl group

  • alpha (a) amino acid

    A compound containing a carboxylic acid group (COOH) as well as an amino group (NH2), both of which are attached to the same carbon atom.

  • amines.

    Organic bases that have the functional group —NR2, where R may be H, an alkyl group, or an aromatic group. (24.4)

  • base ionization constant (Kb).

    The equilibrium constant for the base ionization. (15.6)

  • Brønsted base.

    A substance capable of accepting a proton. (4.3)

  • chemical bond

    A strong attractive force that exists between atoms in a molecule. (Section 8.1)

  • coordinate covalent bond.

    A bond in which the pair of electrons is supplied by one of the two bonded atoms; also called a dative bond. (9.9)

  • cycloalkane

    An alkane whose structure contains a ring.

  • dehydrohalogenation

    An elimination reaction involving the loss of H and a halogen (such as Cl, Br, or I).

  • Electronegativity

    A measure of the force of an atom’s attraction for electrons

  • Hess’s law

    The heat evolved in a given process can be expressed as the sum of the heats of several processes that, when added, yield the process of interest. (Section 5.6)

  • Isotactic polymer

    A polymer with identical confi gurations (either all R or all S) at all chiral centers along its chain, as, for example, isotactic polypropylene

  • Nucleophilic aromatic substitution

    A reaction in which a nucleophile, most commonly a halogen, on an aromatic ring is replaced by another nucleophile.

  • photon

    When electromagnetic radiation is viewed as a particle, an individual packet of energy.

  • photon

    The smallest increment (a quantum) of radiant energy; a photon of light with frequency n has an energy equal to hn. (Section 6.2)

  • racemic mixture

    A solution containing equal amounts of both enantiomers.

  • Thermoplastic

    A polymer that can be melted and molded into a shape that is retained when it is cooled.

  • Thiol

    A compound containing an !SH (sulfhydryl) group bonded to an sp3 -hybridized carbon.

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