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Solutions for Chapter 4.103: 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 4.103: SUMMARY

Solutions for Chapter 4.103
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This textbook survival guide was created for the textbook: Elementary Principles of Chemical Processes, edition: 4. Elementary Principles of Chemical Processes was written by and is associated to the ISBN: 9780470616291. Since 1 problems in chapter 4.103: SUMMARY have been answered, more than 38718 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 4.103: SUMMARY includes 1 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alkenes

    Hydrocarbons containing one or more carbon–carbon double bonds. (Section 24.2)

  • Anti stereoselectivity

    The addition of atoms or groups of atoms to opposite faces of a carbon-carbon double bond.

  • Aprotic acid

    An acid that is not a proton donor; an acid that is an electron pair acceptor in a Lewis acid-base reaction.

  • beta elimination

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

  • boiling point.

    The temperature at which the vapor pressure of a liquid is equal to the external atmospheric pressure. (11.8)

  • Brønsted–Lowry base

    A substance (molecule or ion) that acts as a proton acceptor. (Section 16.2)

  • conduction band

    A band of molecular orbitals lying higher in energy than the occupied valence band and distinctly separated from it. (Section 12.7)

  • dispersion forces

    Intermolecular forces resulting from attractions between induced dipoles. Also called London dispersion forces. (Section 11.2)

  • enolate

    The resonance-stabilized conjugate base of a ketone, aldehyde, or ester.

  • gauche conformation

    A conformation that exhibits a gauche interaction.

  • gauche interaction

    The steric interaction that results when two groups in a Newman projection are separated by a dihedral angle of 60°.

  • High-density lipoprotein (HDL)

    Plasma particles, density 1.06–1.21 g/mL, consisting of approximately 33% proteins, 30% cholesterol, 29% phospholipids, and 8% triglycerides.

  • Hydrophilic

    From the Greek, meaning water-loving.

  • Imide

    A functional group in which two acyl groups, RCO! or ArCO!, are bonded to a nitrogen atom

  • Lewis dot structure

    The symbol of an element surrounded by a number of dots equal to the number of electrons in the valence shell of the atom

  • oxime

    A compound with the structure R2CRN!OH.

  • Pericyclic reaction

    A reaction that takes place in a single step, without intermediates, and involves a cyclic redistribution of bonding electrons

  • physical properties

    Properties that can be measured without changing the composition of a substance, for example, color and freezing point. (Section 1.3)

  • saturated

    A compound that contains no p bonds.

  • termolecular

    For mechanisms, a step that involves three chemical entities.

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