Solutions for Chapter 12.8: Synthesis of Alkylbenzenes by AcylationReduction

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 12.8: Synthesis of Alkylbenzenes by AcylationReduction

Solutions for Chapter 12.8
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Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. Since 1 problems in chapter 12.8: Synthesis of Alkylbenzenes by AcylationReduction have been answered, more than 10956 students have viewed full step-by-step solutions from this chapter. Chapter 12.8: Synthesis of Alkylbenzenes by AcylationReduction includes 1 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Absolute confi guration

    Which of the two possible isomers an enantiomer is (i.e., whether it is the right- or left-handed isomer).

  • aldonic acid

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

  • amino acid residue

    The individual repeating units in a polypeptide chain or protein.

  • chiral

    An object that is not superimposable on its mirror image.

  • critical mass

    The amount of fissionable material necessary to maintain a nuclear chain reaction. (Section 21.7)

  • Glass transition temperature (TG)

    The temperature at which a polymer undergoes the transition from a hard glass to a rubbery state

  • Heterocycle

    A cyclic compound whose ring contains more than one kind of atom. Oxirane (ethylene oxide), for example, is a heterocycle whose ring contains two carbon atoms and one oxygen atom.

  • joule (J)

    The SI unit of energy, 1 kg@m2 >s2. A related unit is the calorie: 4.184 J = 1 cal. (Section 5.1)

  • limiting reactant (limiting reagent)

    The reactant present in the smallest stoichiometric quantity in a mixture of reactants; the amount of product that can form is limited by the complete consumption of the limiting reactant. (Section 3.7)

  • LUMO

    The lowest unoccupied molecular orbital.

  • neutralization reaction

    A reaction in which an acid and a base react in stoichiometrically equivalent amounts; the neutralization reaction between an acid and a metal hydroxide produces water and a salt. (Section 4.3)

  • Phenyl group

    A group derived by removing an H from benzene; abbreviated C6H5! or Ph!.

  • Pro-R-hydrogen

    Replacing this hydrogen by deuterium gives a chiral center with an R confi guration

  • pure substance

    Matter that has a fixed composition and distinct properties. (Section 1.2)

  • quintet

    In NMR spectroscopy, a signal that is comprised of five peaks.

  • radionuclide

    A radioactive nuclide. (Section 21.1)

  • Rate determining step

    The step in a multistep reaction sequence that crosses the highest energy barrier.

  • rem

    A measure of the biological damage caused by radiation; rems = rads * RBE. (Section 21.9)

  • Sulfi de

    The sulfur analog of an ether; a molecule containing a sulfur atom bonded to two carbon atoms. Sulfi des are also called thioethers

  • Tollens’ reagent

    A solution prepared by dissolving Ag2O in aqueous ammonia; used for selective oxidation of an aldehyde to a carboxylic acid.

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