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Solutions for Chapter 12.7: FriedelCrafts Acylation of Benzene

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 12.7: FriedelCrafts Acylation of Benzene

Solutions for Chapter 12.7
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Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Since 2 problems in chapter 12.7: FriedelCrafts Acylation of Benzene have been answered, more than 25612 students have viewed full step-by-step solutions from this chapter. Chapter 12.7: FriedelCrafts Acylation of Benzene includes 2 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • 1,2-elimination

    An elimination reaction in which a proton from the beta (b) position is removed together with the leaving group, forming a double bond.

  • activated complex (transition state)

    The particular arrangement of atoms found at the top of the potential-energy barrier as a reaction proceeds from reactants to products. (Section 14.5)

  • Aromatic compound

    A term used initially to classify benzene and its derivatives. More accurately, it is used to classify any compound that meets the Hückel criteria for aromaticity (Section 21.2A).

  • auxochrome

    When applying Woodward-Fieser rules, the groups attached to the chromophore.

  • condensation polymerization

    Polymerization in which molecules are joined together through condensation reactions. (Section 12.8)

  • conjugate base

    In an acid-base reaction, the product that results when an acid is deprotonated.

  • Delocalization

    The spreading of electron density over a larger volume of space.

  • 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

  • extensive property

    A property that depends on the amount of material considered; for example, mass or volume. (Section 1.3)

  • Haworth projection

    A way to view furanose and pyranose forms of monosaccharides. The ring is drawn fl at and most commonly viewed through its edge with the anomeric carbon on the right and the oxygen atom of the ring to the rear

  • ion-product constant

    For water, Kw is the product of the aquated hydrogen ion and hydroxide ion concentrations: 3H+43OH-4 = Kw = 1.0 * 10-14 at 25 °C. (Section 16.3)

  • ketone

    A compound in which the carbonyl group 1C “O2 occurs at the interior of a carbon chain and is therefore flanked by carbon atoms. (Section 24.4)

  • lipid

    Naturally occurring compoundsthat can be extracted from cells usingnonpolar organic solvents.

  • oxyanion

    A polyatomic anion that contains one or more oxygen atoms. (Section 2.8)

  • proteins

    Polypeptide chains comprised of more than 40 or 50 amino acids.

  • pyranose ring

    A six-membered cyclic hemiacetal form of a carbohydrate.

  • radiotracer

    A radioisotope that can be used to trace the path of an element in a chemical system. (Section 21.5)

  • sp2-hybridized orbitals

    Atomic orbitals that are achieved by mathematically averaging one s orbital with two p orbitals to form three hybridized atomic orbitals.

  • syn addition

    An addition reaction in which two groups are added to the same face of a p bond.

  • 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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