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Solutions for Chapter 4.77: 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 4.77: SUMMARY

Solutions for Chapter 4.77
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This textbook survival guide was created for the textbook: Elementary Principles of Chemical Processes, edition: 4. Chapter 4.77: SUMMARY includes 1 full step-by-step solutions. Since 1 problems in chapter 4.77: SUMMARY have been answered, more than 41984 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. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • 1,2-Shift

    A type of rearrangement in which an atom or group of atoms with its bonding electrons moves from one atom to an adjacent electron-defi cient atom.

  • atom.

    The basic unit of an element that can enter into chemical combination. (2.2)

  • cation

    A positively charged ion. (Section 2.7)

  • Chain-transfer reaction

    The transfer of reactivity of an endgroup from one chain to another during a polymerization

  • chemically equivalent

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

  • conformation

    A three-dimensional shape that can be adopted by a compound as a result of rotation about single bonds.

  • electronegativity

    A measure of the ability of an atom that is bonded to another atom to attract electrons to itself. (Section 8.4)

  • ether

    A compound with the structure R!O!R.

  • half-life

    The time required for the concentration of a reactant substance to decrease to half its initial value; the time required for half of a sample of a particular radioisotope to decay. (Sections 14.4 and 21.4)

  • inversion of configuration

    During a reaction, when the configuration of a chirality center is changed.

  • Lipid bilayer

    A back-to-back arrangement of phospholipid monolayers, often forming a closed vesicle or membrane.

  • Peptide bond

    The special name given to the amide bond formed between the a-amino group of one amino acid and the a-carboxyl group of another amino acid

  • periplanar

    A conformation in which a hydrogen atom and a leaving group are approximately coplanar.

  • pH

    The negative log in base 10 of the aquated hydrogen ion concentration: pH = -log3H+4. (Section 16.4)

  • Polynuclear aromatic hydrocarbon (PAH)

    A hydrocarbon containing two or more fused benzene rings

  • Polysaccharide

    A carbohydrate containing a large number of monosaccharide units, each joined to the next by one or more glycosidic bonds.

  • primary

    A term used to indicate that exactly one alkyl group is attached directly to a particular position. For example, a primary carbocation has one alkyl group (not more) attached directly to the electrophilic carbon atom (C+).

  • reducing agent, or reductant

    The substance that is oxidized and thereby causes the reduction of some other substance in an oxidation–reduction reaction. (Section 20.1)

  • singlet

    In NMR spectroscopy, a signal that is comprised of only one peak.

  • Unimolecular reaction

    A reaction in which only one species is involved in the rate-determining step

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