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Solutions for Chapter 22.1: THE NOMENCLATURE OF AMINO ACIDS

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 22.1: THE NOMENCLATURE OF AMINO ACIDS

Organic Chemistry was written by and is associated to the ISBN: 9780321803221. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Since 5 problems in chapter 22.1: THE NOMENCLATURE OF AMINO ACIDS have been answered, more than 38131 students have viewed full step-by-step solutions from this chapter. Chapter 22.1: THE NOMENCLATURE OF AMINO ACIDS includes 5 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
  • Axial bond

    A bond to a chair conformation of cyclohexane that extends from the ring parallel to the imaginary axis through the center of the ring; a bond that lies roughly perpendicular to the equator of the ring.

  • bomb calorimeter

    A device for measuring the heat evolved in the combustion of a substance under constant-volume conditions. (Section 5.5)

  • bond enthalpy

    The enthalpy change, ?H, required to break a particular bond when the substance is in the gas phase. (Section 8.8)

  • chemically equivalent

    In NMR spectroscopy, protons (or carbon atoms) that occupy identical electronic environments and produce only one signal.

  • degenerate

    Having the same energy.

  • Dipole-dipole interaction

    The attraction between the positive end of one dipole and the negative end of another.

  • Double-headed arrow

    A symbol used to show that structures on either side of it are resonance-contributing structures

  • electrophilic aromatic substitution

    A substitution reaction in which an aromatic proton is replaced by an electrophile and the aromatic moiety is preserved.

  • leveling effect

    An effect thatprevents the use of bases stronger than hydroxidewhen the solvent is water.

  • lithium dialkyl cuprate

    A nucleophilic compound with the general structureR2CuLi.

  • Meisenheimer complex

    Theresonance-stabilized intermediate of a nucleophilicaromatic substitution reaction.

  • organic chemistry

    The study of carbon-containing compounds, typically containing carbon–carbon bonds. (Section 2.9; Chapter 24:Introduction)

  • peroxides

    Compounds with the general structure R!O!O!R.

  • primary cell

    A voltaic cell that cannot be recharged. (Section 20.7)

  • prostaglandins

    Lipids that contain 20 carbon atoms and are characterized by a five-membered ring with two side chains.

  • rate constant

    A constant of proportionality between the reaction rate and the concentrations of reactants that appear in the rate law. (Section 14.3)

  • SN2

    A bimolecular nucleophilic substitution reaction.

  • tertiary structure

    The threedimensional shape of a protein.

  • Thiol

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

  • Ylide

    A neutral molecule with positive and negative charges on adjacent atoms

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