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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 27658 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
  • aldose

    A carbohydrate that contains an aldehyde group.

  • bond order

    The number of bonding electron pairs shared between two atoms, minus the number of antibonding electron pairs: bond order = (number of bonding electrons - number of antibonding electrons)/2. (Section 9.7)

  • Bonding electrons

    Valence electrons involved in forming a covalent bond (i.e., shared electrons).

  • chain-growth polymer

    A polymer that is formed under conditions in which the monomers do not react directly with each other, but rather, each monomer is added to the growing chain, one at a time.

  • chemical formula.

    An expression showing the chemical composition of a compound in terms of the symbols for the atoms of the elements involved. (2.6)

  • chlorophyll

    A plant pigment that plays a major role in conversion of solar energy to chemical energy in photosynthesis. (Section 23.3)

  • dienophile

    A compound that reacts with a diene in a Diels-Alder reaction.

  • E (Section 5.2C)

    From the German, entgegen, opposite. Specifi es that groups of higher priority on the carbons of a double bond are on opposite sides

  • exothermic

    Any process with a negative DH (the system gives energy to the surroundings).

  • isotopes

    Atoms of the same element containing different numbers of neutrons and therefore having different masses. (Section 2.3)

  • N-glycoside

    The product obtained when a monosaccharide is treated with an amine in the presence of an acid catalyst.

  • Photolysis

    Cleavage by light.

  • Polyamide

    A polymer in which each monomer unit is joined to the next by an amide bond, as, for example, nylon 66.

  • primary structure

    The sequence of amino acids along a protein chain. (Section 24.7)

  • Protic solvent

    A solvent that is a hydrogen-bond donor. Common protic solvents are water, low-molecular-weight alcohols, and low-molecular weight carboxylic acids.

  • Reaction coordinate diagram

    A graph showing the energy changes that occur during a chemical reaction; energy is plotted on the vertical axis and reaction progress is plotted on the horizontal axis.

  • reaction mechanism

    A detailed picture, or model, of how the reaction occurs; that is, the order in which bonds are broken and formed and the changes in relative positions of the atoms as the reaction proceeds. (Section 14.6)

  • reductive amination

    The conversion of a ketone or aldehyde into an imine under conditions in which the imine is reduced as soon as it is formed, giving an amine.

  • sigma 1S2 bond

    A covalent bond in which electron density is concentrated along the internuclear axis. (Section 9.6)

  • zwitterion

    A net neutral compound that exhibits charge separation. Amino acids exist as zwitterions at physiological pH.

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