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Solutions for Chapter 4.17: SUMMARY

Elementary Principles of Chemical Processes | 4th Edition | ISBN: 9780470616291 | Authors: Richard M. Felder Ronald W. Rousseau, Lisa G. Bullard

Full solutions for Elementary Principles of Chemical Processes | 4th Edition

ISBN: 9780470616291

Elementary Principles of Chemical Processes | 4th Edition | ISBN: 9780470616291 | Authors: Richard M. Felder Ronald W. Rousseau, Lisa G. Bullard

Solutions for Chapter 4.17: SUMMARY

Solutions for Chapter 4.17
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This textbook survival guide was created for the textbook: Elementary Principles of Chemical Processes, edition: 4. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 4.17: SUMMARY includes 1 full step-by-step solutions. Since 1 problems in chapter 4.17: SUMMARY have been answered, more than 23324 students have viewed full step-by-step solutions from this chapter. Elementary Principles of Chemical Processes was written by and is associated to the ISBN: 9780470616291.

Key Chemistry Terms and definitions covered in this textbook
  • accuracy.

    The closeness of a measurement to the true value of the quantity that is measured. (1.8)

  • 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)

  • alkylthio group

    An SR group.

  • Annulene

    A cyclic hydrocarbon with a continuous alternation of single and double bonds.

  • dash

    In bond-line structures, agroup going behind the page.

  • enantiomerically pure

    A substance that consists of a single enantiomer, and not its mirror image.

  • fibrous proteins

    Proteins that consist of linear chains that are bundled together.

  • intermediate

    A structure corresponding to a local minimum (valley) in an energy diagram.

  • lactone

    A cyclic ester.

  • levorotatory

    A compound thatrotates plane-polarized light in a counterclockwisedirection (-).

  • ozonolysis

    A reaction in which the CRC bond of an alkene is cleaved to form two CRO bonds.

  • polar aprotic solvent

    A solvent that lacks hydrogen atoms connected directly to an electronegative atom.

  • polysaccharides

    Polymers made up of repeating monosaccharide units linked together by glycoside bonds.

  • Polyurethane

    A polymer containing the !NHCO2! group as a repeating unit

  • product

    A substance produced in a chemical reaction; it appears to the right of the arrow in a chemical equation. (Section 3.1)

  • radical initiator

    A compound with a weak bond that undergoes homolytic bond cleavage with great ease, producing radicals that can initiate a radical chain process.

  • Reaction mechanism

    A step-by-step description of how a chemical reaction occurs.

  • retro Diels-Alder reaction

    The reverse of a Diels-Alder reaction, achieved at high temperature. A cyclohexene derivative is converted into a diene and a dienophile.

  • sp2-hybridized orbitals

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

  • steroids

    Lipids that are based on a tetracyclic ring system involving three six-membered rings and one five-membered ring. Cholesterol is an example.

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