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Solutions for Chapter 19.5: Nucleophilic Acyl Substitution in Acid Anhydrides

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 19.5: Nucleophilic Acyl Substitution in Acid Anhydrides

Solutions for Chapter 19.5
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This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. Since 1 problems in chapter 19.5: Nucleophilic Acyl Substitution in Acid Anhydrides have been answered, more than 32271 students have viewed full step-by-step solutions from this chapter. Chapter 19.5: Nucleophilic Acyl Substitution in Acid Anhydrides includes 1 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9.

Key Chemistry Terms and definitions covered in this textbook
  • alkali metals.

    The Group 1A elements (Li, Na, K, Rb, Cs, and Fr). (2.4)

  • anomeric carbon

    The C1 position of the cyclic hemiacetal of an aldose or the C2 position of the cyclic hemiacetal of a ketose.

  • aromatic hydrocarbons

    Hydrocarbon compounds that contain a planar, cyclic arrangement of carbon atoms linked by both s and delocalized p bonds. (Section 24.2)

  • atomic weight

    The average mass of the atoms of an element in atomic mass units (amu); it is numerically equal to the mass in grams of one mole of the element. (Section 2.4)

  • biochemistry

    The study of the chemistry of living systems. (Chapter 24: Introduction)

  • corrosion.

    The deterioration of metals by an electrochemical process. (18.7)

  • electron density

    The probability of finding an electron at any particular point in an atom; this probability is equal to c2, the square of the wave function. Also called the probability density. (Section 6.5)

  • elimination

    A reaction involving the loss of a leaving group and formation of a p bond.

  • energy of activation

    In an energy diagram, the height of the energy barrier (the hump) between the reactants and the products.

  • epoxide

    A cyclic ether containing a three-membered ring system. Also called an oxirane (also see Sect. 14.7).

  • fragmentation

    In mass spectrometry, when the molecular ion breaks apart into fragments.

  • halohydrin formation

    A reaction which involves the addition of a halogen and a hydroxyl group (OH) across an alkene.

  • hydrogen bonding

    A special type of dipole-dipole interaction that occurs between an electronegative atom and a hydrogen atom that is connected to another electronegative atom.

  • N-bromosuccinimide

    A reagent used for allylic bromination to avoid a competing reaction in which bromine adds across the p bond.

  • nitrous acid

    A compound with molecular formula HONO.

  • organohalide

    An organic compound containing at least one halogen.

  • peptide

    A chain comprised of a small number of amino acid residues.

  • radioactive

    Possessing radioactivity, the spontaneous disintegration of an unstable atomic nucleus with accompanying emission of radiation. (Section 2.2; Chapter 21: Introduction)

  • sigma 1S2 molecular orbital

    A molecular orbital that centers the electron density about an imaginary line passing through two nuclei. (Section 9.7)

  • Stork enamine synthesis

    A Michaelreaction in which an enamine functions as anucleophile.

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