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Organic Chemistry 7th Edition - Solutions by Chapter

Organic Chemistry | 7th Edition | ISBN: 9781133952848 | Authors: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9781133952848

Organic Chemistry | 7th Edition | ISBN: 9781133952848 | Authors: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Organic Chemistry | 7th Edition - Solutions by Chapter

The full step-by-step solution to problem in Organic Chemistry were answered by Patricia, our top Chemistry solution expert on 03/16/18, 05:02PM. This expansive textbook survival guide covers the following chapters: 24. Organic Chemistry was written by Patricia and is associated to the ISBN: 9781133952848. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Since problems from 24 chapters in Organic Chemistry have been answered, more than 3015 students have viewed full step-by-step answer.

Key Chemistry Terms and definitions covered in this textbook
  • acidic cleavage

    A reaction in which bonds are broken in the presence of an acid. For example, in the presence of a strong acid, an ether is converted into two alkyl halides.

  • bond enthalpy

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

  • Cation

    An atom or group of atoms bearing a positive charge.

  • Conjugate acid

    The species formed when a base accepts a proton from an acid

  • cyanides.

    Compounds containing the CN2 ion. (22.3)

  • dash

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

  • diastereomers

    Stereoisomers that are not mirror images of one another.

  • Electrophoresis

    The process of separating compounds on the basis of their electric charge

  • equivalence point

    The point in a titration at which the added solute reacts completely with the solute present in the solution. (Section 4.6)

  • Fischer projection

    A twodimensional representation of a molecule; in these projections, groups on the right and left are by convention in front, while those at the top and bottom are to the rear.

  • gas constant (R)

    The constant of proportionality in the ideal-gas equation. (Section 10.4)

  • hydrogen deficiency index (HDI)

    A measure of the number of degrees of unsaturation in a compound.

  • monomers

    Molecules with low molecular weights, which can be joined together (polymerized) to form a polymer. (Section 12.8)

  • N-bromosuccinimide

    A reagent used for allylic bromination to avoid a competing reaction in which bromine adds across the p bond.

  • 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

  • polar aprotic solvent

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

  • Potential energy

    The energy that can be released if given an opportunity

  • rate-determining step

    The sloweststep in a multistep reaction which determines the rate of the reaction.

  • solvent extraction

    A process by which one or more compounds are removed from a mixture of organic compounds, based on a difference in solubility and/or acid-base properties.

  • Transfer RNA (tRNA

    A ribonucleic acid that carries a specifi c amino acid to the site of protein synthesis on ribosomes

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